Protein Machineries Involved in the Attachment of Heme to Cytochrome c: Protein Structures and Molecular Mechanisms

Cytochromes c (Cyt c) are ubiquitous heme-containing proteins, mainly involved in electron transfer processes, whose structure and functions have been and still are intensely studied. Surprisingly, our understanding of the molecular mechanism whereby the heme group is covalently attached to the apoprotein (apoCyt) in the cell is still largely unknown. This posttranslational process, known as Cyt c biogenesis or Cyt c maturation, ensures the stereospecific formation of the thioether bonds between the heme vinyl groups and the cysteine thiols of the apoCyt heme binding motif. To accomplish this task, prokaryotic and eukaryotic cells have evolved distinctive protein machineries composed of different proteins. In this review, the structural and functional properties of the main maturation apparatuses found in gram-negative and gram-positive bacteria and in the mitochondria of eukaryotic cells will be presented, dissecting the Cyt c maturation process into three functional steps: (i) heme translocation and delivery, (ii) apoCyt thioreductive pathway, and (iii) apoCyt chaperoning and heme ligation. Moreover, current hypotheses and open questions about the molecular mechanisms of each of the three steps will be discussed, with special attention to System I, the maturation apparatus found in gram-negative bacteria.


Introduction
Cytochromes c (Cyts c) are ubiquitous heme-containing proteins involved in a variety of critical processes of cellular metabolism; since their discovery by Keilin in the early 1920s, they have been the focus of multidisciplinary scientific interests and nowadays are considered textbook proteins in biochemistry courses. However, many aspects of c-type cytochromes are still to be unveiled, from the control and fine-tuning of electron transfer reactions and heme reactivity [1][2][3] to the description of Cyt c folding pathways and stability [4][5][6]. The presence of the covalently bound heme prosthetic group dictates the functions of Cyts c, which are associated mainly with electron transfer processes in aerobic and anaerobic respiration and in photosynthesis [7,8]; however, it is now clear that Cyts c play important roles also in other cellular processes such as H 2 O 2 scavenging, cytochrome c oxidase assembly [9], lipid signaling [10], or apoptotic processes in the eukaryotic cells [11,12]. This review deals with a complex and still largely unknown process, whereby the heme is covalently and stereospecifically attached to the apoprotein (apoCyt) in the cell; this posttranslational process is known as Cyt c biogenesis or Cyt c maturation. Over and above its scientific relevance, a full understanding of this posttranslational process may pave the way for future biotechnological applications, such as the design and the production in vivo of novel heme-proteins and biosensors endowed with innovative redox functions [13].
The heme b (Fe-protoporphyrin IX) is synthesized in prokaryotes and eukaryotes along a conserved pathway with highly related enzymes and biosynthetic intermediates [14]; heme c is defined as a heme b, covalently linked to the protein by thioether bonds (Figure 1). In bacteria, heme biosynthesis occurs in the cytoplasm and the final step is the insertion of iron into protoporphyrin IX by ferrochelatase; in the eukaryotic cell, the heme biosynthetic pathway is splitted between the cytosol and the mitochondrion: here, at the level of the mitochondrial inner membrane, the ferrochelatase enzyme catalyzes the heme iron insertion. Although the heme biosynthetic pathway is well characterized, the molecular Figure 1: The heme-binding site typically observed in c-type cytochromes, as exemplified by a close-up view of the structure of P. aeruginosa Cyt c551 (Pa-Cytc; PDB 351c). The heme is shown in red, while the atoms of the residues from the heme-binding motif of Pa-Cytc (C 12 VAC 15 H) and the distal Met61 are color-coded (C: green; O: red; N: blue; S: yellow). The figure highlights the thioether bonds between the Cys12 (on the right) and the vinyl-2, and between Cys15 (on the left) and the vinyl-4. The iron atom of the heme (in gray) is axially coordinated by the distal methionine residue (Met61; shown above the heme plane) and by the proximal histidine residue (His16; shown below the heme plane). mechanism(s) underlying the process of heme trafficking across the membranes is still largely obscure (see [15,16] for reviews on heme synthesis and trafficking in eukaryotes). In all known Cyts c, the heme is covalently linked to the apoCyt with the same stereochemistry: two thioether bonds are present between the vinyls at positions 2 and 4 of the tetrapyrrole ring of heme b and the thiols of the N-and C-terminal cysteines (Cys1 and Cys2, resp.) of a conserved heme-binding motif (C1XXC2H, where X denotes any residues). The iron atom of the Fe-protoporphyrin IX is always axially coordinated to the histidine of the heme-binding motif (on the proximal side of the heme cavity), while a methionine residue on the distal side generally represents the second axial ligand ( Figure 1). C-type cytochromes may contain more than one heme c linked to the protein through different C1XXC2H motifs. From a structural point of view, Cyt c proteins define a well-defined -helical fold (see SCOP-http://scop.mrclmb.cam.ac.uk/scop/ and CATH-http://www.cathdb.info/ protein structure databases), characterized by the presence of three -helices: the N-and C-terminal -helices interact each other in the native structure, while an additional -helix (historically known as the 60 helix) overlays part of the heme cavity. Since the seminal experiment of Anfinsen on horse heart Cyt c [17], it is generally accepted that Cyt c without its covalently bound heme (apoCyt) is an unfolded protein, devoid of appreciable secondary and tertiary structure and that the polypeptide chain is able to fold into its typical Cyt c structure only when the thioether bonds with the heme are formed. As it will be discussed below, these observations raise interesting questions as to how an unfolded protein such as apoCyt, is specifically recognized by the different protein components of the maturation apparatus of the cell. Recently, however, evidence has been presented that, at least in some cases, the Cyt c fold may be attained even in the absence of the heme [18], challenging our current view of the Cyt c folding mechanism [4,19].
C-type cytochromes are synthesized in the cytoplasm (nside of the membrane), but they exert their functions in other subcellular compartments (p-side of the membrane), that is, the periplasm of gram-negative bacteria, the bacterial extracytoplasmic space of gram-positive bacteria, the intermembrane space-IMS, of mitochondria, or the chloroplast thylakoid lumen. It is in these subcellular compartments that the heme b is covalently attached to apoCyt by the appropriate maturation apparatus. In prokaryotes, the necessary translocation of apoCyt across the membrane is carried out by the Sec machinery [26]; this apparatus, composed of the SecAB-DYEFG proteins, is able to translocate unfolded proteins carrying a specific targeting sequence [27]. In eukaryotes, the newly synthesized apoCyt is probably translocated into the mitochondrion via a different mechanism involving components of the TOM complex on the outer side of the membrane and the cytochrome c heme lyase, which probably acts also as an apoCyt receptor in the mitochondrial IMS [28,29]. However, the process is not completely clear, as we still do not know whether the apoCyt is delivered to the mitochondrial matrix and then exported to the IMS [30] or it is translocated directly to the IMS via a different mechanism [31]. It should be noticed that in plants, the translocation of c-type cytochromes into the chloroplast lumen is probably independent on the heme attachment reaction [32,33].
Despite that in all c-type cytochromes, both prokaryotic or eukaryotic, the heme is always covalently linked to the conserved CXXCH heme-binding motif, different maturation apparatuses composed of different proteins have been identified ( [34,35]; see Figures 2, 3, and 4 and Table 1). Structural and functional properties of the protein components of Systems I-III are the focus of the present review; other maturation apparatuses, involved in the unusual attachment of heme b to the protein moiety via a single thioether bond (Systems IV-VI), have been described and reviewed elsewhere [36,37].
With the exception of system III which is present in eukaryotic cells, the distribution of the other Systems among Bacteria, Archaea, and plant cells is complicated by the observation that in many cases, the maturation machinery is not conserved [38], rendering the analysis of their evolutionary origins and relationships difficult [39][40][41]. In -andproteobacteria, in some -and -proteobacteria, in Archaea and in the mitochondria of plants and algae, Cyt c maturation is carried out by a set of eight or nine proteins belonging to System I [42] (Figure 2); in gram-positive bacteria, in cyanobacteria, in the chloroplasts of plants and algae, in -, -and some -proteobacteria the Cyt c maturation process is carried out by three or four proteins belonging to System II [43,44] (Figure 3), while System III occurs in mitochondria of fungi, metazoans, and some protozoa [16,45] (Figure 4) [21], 3KH7 [22], and 2HL7 [23], resp.). Organisms employing System I: -and -proteobacteria, some -proteobacteria (e.g., Nitrosomonas) and -proteobacteria (e.g., Desulfovibrio), and Deinococci and Archaea. Additionally, System I is observed in plant mitochondria and in the mitochondria of some protozoa (e.g., Tetrahymena).
(System I in mitochondria, System III in the p-side of the thylakoid membrane, and System IV in the n-side of the thylakoid membrane [16,38]) makes the classification and the distribution of the different maturation systems even more difficult. With the exception of System III, which is apparently composed of a single protein able to carry out the different tasks of the Cytc maturation process (see below), the various proteins of Systems I and II carry out different functions, including the translocation and delivery of heme b from the cytoplasm where it is synthesized to the relevant subcellular compartment, the chaperoning of apoCyt and the reduction of its disulfide, the formation of the covalent bonds between the heme b and the CXXCH heme-binding motif of the apoprotein ( Table 1). The complexity of System I, compared to the protein composition of other Cyt c maturation systems, has long been discussed; in particular, it has been proposed that a possible explanation is to be found in the ability evolved by organisms employing System I to utilize lower levels of endogenous heme than those necessary for organisms which evolved Systems II or III [46].

System I
The proteins belonging to System I (named CcmABCDE-FGH(I), from Cytochrome c maturation), are membrane proteins exposing their soluble domains (when present) into the periplasm ( Figure 2). All of these proteins are encoded by a single operon in -, -, and -proteobacteria [42,47]. The availability of the entire Ccm operon in a single  [24]. System II is found in plant chloroplasts, in gram-positive bacteria, cyanobacteria,proteobacteria, most -proteobacteria (e.g., Bordetella, Burkholderia), and some -proteobacteria (e.g., Geobacter).

Heme
Intermembrane space

Inner membrane
Outer membrane Cyt c apoCyt HCCS Figure 4: Schematic representation of System III. A single protein (HCCS) associated to the mitochondrial inner membrane is required for Cyt c maturation. The translocation process of heme (shown in red) is unknown. System III is found in the mitochondria of fungi (e.g., S. cerevisiae), vertebrates (e.g., human), and invertebrates (e.g., C. elegans, Drosophila).
plasmid (pEC86; [48]) greatly facilitated the heterologous over-expression of many c-type cytochromes in E. coli [49]. Apparently, c-type cytochromes specificity of the Ccm apparatus is rather low; indeed, in an attempt to characterize the minimal sequence requirements of the apoCyt polypeptide recognized by System I, it was shown that this complex multiprotein apparatus is able to attach the heme even to short, microperoxidase-like peptides carrying the CXXCH motif [50].
As discussed below, different studies, mainly carried out by immunoprecipitation experiments, suggest that the Ccm proteins may be assembled in the bacterial membrane in a maturase multiprotein complex(es). However, the existence and/or stoichiometry of these complexes remains to be determined, either because of the experimental difficulties in handling membrane protein complexes, or because it is possible that these complexes are unstable and only transiently populated. Independently from their functional existence in the bacterial periplasm as independent units or as components of a multisubunit complex, it is clear that each of the Ccm proteins plays a different role, from the transport and chaperoning of the heme cofactor, to the necessary reduction of the disulfide bond between the sulfur atoms of the two Cys residues of the conserved CXXCH motif of apoCyt, and finally to the catalysis of covalent heme attachment. An additional interesting aspect is that, over and above their role in the biogenesis of Cytc, there is also evidence that inactivation of some ccm genes induces phenotypes that cannot be explained only in terms of absence of synthesis of Cyt c; all of these pleiotropic effects are linked to impairment of heme and/or iron trafficking in the periplasm [47]. In particular, it has been recently shown that, in -andproteobacteria (including the human opportunistic pathogen P. aeruginosa), mutations in the ccmC, ccmI and ccmF genes induce phenotypes such as reduced pyoverdine production, reduced bacterial motility or impaired growth in lowiron conditions ( [51] and refs. therein). These observations, suggesting that Ccm proteins perform additional functions critical for bacterial physiology, growth and virulence, provide a rationale to explain why bacteria, at variance with the eukaryotic cell, have evolved a metabolically expensive operon to accomplish an apparently simple task such as heme ligation to apoCyt. Novel hypotheses addressing these aspects and awaiting experimental investigation include (i) the utilization of Ccm-associated heme for additional cellular processes besides attachment to apoCyt, (ii) trafficking a nonheme compound through the Ccm system required for iron acquisition such a siderophore, (iii) the Ccm inactivationdependent accumulation of heme b, a photoreactive molecule whose degradation leads to reactive oxygen species, and (iv) the destructive effect on [Fe-S] clusters of ferrisiderophores reductases.
In the following, the structural (when known) and functional properties of the different components of the System I maturation apparatus will be discussed, dissecting the Cytc maturation process into three main functional steps: heme translocation and delivery, apoCyt thioreductive pathway, and apoCyt chaperoning and heme ligation (a similar modular description can also be found elsewhere (see [34,52])). However, it should be remembered that in many cases the proteins involved in the three steps are not uniquely assigned to a specific module, as they interact with each other; moreover, it has been shown that, in some cases, more than one system can be present [41]. This modular organization of Cyt c biogenesis should therefore be intended only as a way to simplify the description of an overall, highly integrated process. For each of the three functional steps, presentation of the structural and functional properties of the different protein components is followed by a discussion of the proposed molecular mechanism(s).

System I: Components of the Heme Translocation and
Delivery Pathway. CcmA and CcmB proteins show the typical sequence features of the ABC (ATP binding Cassette) transporter family and therefore these components of System I were initially considered as the proteins responsible for the translocation of the newly synthesized heme from the cytoplasm to the periplasmic space. ABC transporters are ubiquitous, multidomain integral membrane proteins that translocate a large variety of substrates across cellular membranes using ATP hydrolysis as a source of energy; they are generally composed of a transmembrane (TM) domain and a conserved cytosolic nucleotide-binding domain [53].
CcmA is a cytoplasmic soluble protein, representing the nucleotide-binding domain of the hypothetical ABC transporter; according to this hypothesis, its sequence contains a nucleotide-binding domain and Walker A and B motifs for ATP hydrolysis [46]. It has also been shown that CcmA possesses ATPase activity in vitro and that the protein is associated with the membrane fraction only when CcmB is also present [54].
CcmB and CcmC are both integral membrane proteins predicted to contain six TM helices. CcmC contains a short WWD domain in its second periplasmic domain and belongs to the heme handling protein family (HHP) [55]. WWD domains are short, tryptophan-rich, aminoacid stretches with the conserved WGX WXWDXRLT sequence (where represents an aromatic amino acid residue and X represents any residue) [40,56]; it has been proposed that proteins containing WWD domains are involved in heme-binding and, as we will see below, a WWD domain is also present in the CcmF protein, another crucial heme-binding protein of System I. CcmC also contains two absolutely conserved histidine residues in its first (between TM helices 1 and 2) and third (between TM helices 5 and 6) periplasmic domains. An attractive hypothesis, still requiring experimental proof, is that the hydrophobic residues within the tryptophan-rich motif provide a platform for the binding of heme, whereas the two conserved His residues (H60 and H184 in E. coli CcmC) act as axial heme ligands [57]; this hypothesis is strengthened by the observation that CcmC indeed interacts directly with heme [58,59]. Immunoprecipitation experiments have shown that in E. coli, CcmABC proteins form a multiprotein complex with a CcmA 2 CcmB 1 CcmC 1 stoichiometry, confirming that these components form an ABCtype transporter complex with unusual functional properties associated to the release of holoCcmE from CcmC [41,46], rather than to heme transport per se. CcmC is an interesting protein, worth of future experimental efforts, as it is known that in some pathogenic bacteria, CcmC mutations are associated to specific phenotypes apparently not related to Cyt c maturation, such as siderophore production in Paracoccus and Pseudomonas [51] and iron utilization in Legionella [60].
Limited information is available about the structure and function of CcmD, which appears to be a small membrane protein (about 70 aminoacid residues) with no conserved sequence features, whose topology is currently debated; contrary to the original proposal [61], additional experiments have shown that in E. coli and R. capsulatus, CcmD is an integral membrane protein composed of a single TM helix, a periplasmic-oriented N-terminus, and a cytoplasmicoriented C-terminus [62]. Immunoprecipitation experiments indicate that CcmD interacts with the CcmA 2 CcmB 1 CcmC 1 complex; even if it is not essential for heme transfer and attachment from CcmC to CcmE, CcmD is strictly required for the release of holoCcmE from the ABC transporter [61,62].
CcmE is a heme-binding protein, discovered as an essential System I component as early as the late 1990's [63]. CcmE is a monotopic membrane protein, anchored to the membrane via its N-terminal TM segment and exposing its active site to the periplasm; it is the only Ccm component of the heme trafficking and delivery module of System I for which a three-dimensional structure is available ( [21] PDB: 1SR3; [64] PDB: 1LM0). The 3D structure of the apo-state (without bound heme) consists of a six-stranded antiparallel -sheet, reminiscent of the classical OB-fold [65] with Nand C-terminal extensions. CcmE can be considered a "heme chaperone, " as it protects the cell from a potentially dangerous compound by sequestering free heme in the periplasm [66]; it is thought to act as an intermediate in the heme delivery pathway of Cytc maturation. The structure of apoCcmE showed no recognizable heme-binding cavities and, in the absence of a 3D structure of CcmE with bound heme (holoC-cmE), the heme-binding region could only be predicted by in silico modeling. It is generally believed that the heme in holoCcmE is solvent exposed, but recent mutagenesis experiments challenged this view [67]. The unusual covalent bond between the nitrogen atom of a histidine residue present in the conserved VLAKHDE motif located in a solvent exposed environment (H130 in E. coli CcmE) and a -carbon of one of the heme vinyl groups has been described in great detail by NMR spectroscopy [68]. Recently, it was shown that CcmE proteins from the proteobacteria D. desulfuricans and D. vulgaris contain the unusual CXXXY heme-binding motif, where the Cys residue replaces the canonical His binding residue. NMR solution structure of D. vulgaris CcmE (PDB: 2KCT) revealed that the proteins adopt the same OB-fold characteristic of the CcmE superfamily. Contrary to what reported for the D. desulfuricans CcmE [69], the homologous protein from D. vulgaris binds ferric heme noncovalently through the conserved C127 residue [70]. An additional conserved residue in CcmE proteins is Tyr134, which was shown to provide a coordination bond to the heme iron of holoCcmE [71,72] once it is released from CcmABCD complex [36], as discussed below.

System I: Heme Translocation and Delivery Pathway
Mechanisms. We still do not know how the b heme is translocated from the cytoplasm (where it is synthesized) to the periplasm, where Cyt c maturation occurs. Different mechanisms such as translocation through a protein channel or free diffusion across the membrane have been proposed [73]. The CcmAB proteins show structural features typical of the ABC transporters and for these reasons, they were originally hypothesized to be involved in the heme b translocation process [57,63,74,75]. However, it is now clear that an alternative process must exist, since it has been shown that periplasmic b-type cytochromes can be produced in the absence of Ccm proteins [76] and that inactivation of the ATPase activity of CcmA does not abolish heme accumulation in the periplasm [46,54]. We have now evidence that CcmC has the ability to bind heme at its WWD domain present in the second periplasmic domain, but it is still not clear if this membrane protein acts as a protein channel for heme translocation, or simply collects it in the periplasm [77].
Another important aspect concerns the oxidation state of the heme iron during translocation and delivery processes; indeed, this property of the heme iron may determine the reaction mechanism by which the unusual CcmE H130 nitrogen is covalently linked to the vinyl -carbon of the heme (see [36] for a detailed discussion of this topic). Based on mutagenesis studies on CcmC [59], a model has been presented whereby oxidized heme is bound to CcmC only in the presence of CcmE, forming a ternary complex. Both CcmC and CcmE provide critical residues for heme-binding: the two conserved His residues (H60 and H180, coordinating the heme iron) and the WWD domain of CcmC and His130 of CcmE, forming the unusual covalent bond with heme vinyl-2 [59]. The ATPase activity of CcmA is then required to release holoCcmE from the CcmABCD complex, a process that depends also on the presence of CcmD [46,54]. It should be noticed that purified holoCcmE alone or in the CcmCDE complex [36,59] contains the heme iron in the oxidized state, an observation that is apparently in contrast with the fact that the heme must be in its reduced state before attachment to apoCyt can occur. Although the oxidation state of the heme iron is currently debated [36,78], it is possible that CcmF, which was recently shown to contain a heme b cofactor, may act as specific heme oxidoreductase (see Section 2.5).

System I: ApoCyt Thioreduction Pathway Components.
The periplasm can be considered a relatively oxidizing environment, due to the presence of an efficient oxidative system composed of the DsbAB proteins [79,80]. DsbA is a highly oxidizing protein ( 0 = 120 mV) that is responsible for the introduction of disulfide bonds into extracytoplasmic proteins [81]. On the basis of the results obtained on E. coli dsbA deletion mutants that are unable to synthesize c-type cytochromes [82,83], it was generally accepted that formation of the intramolecular disulfide bond in apoCyt was a necessary step in the Cyt c biogenesis. However, only reduced apoCyt is clearly competent for heme ligation. It is possible that this seemingly paradoxical thioreduction process has evolved in order to protect the apoCyt from proteolytic degradation, aggregation, and/or formation of intermolecular disulfide bonds with thiols from other molecules (see also Section 3.1 for a discussion about this aspect in System II). Recently, however, an analysis of c-type cytochromes production in several E. coli dsb genes deletion strains led to the hypothesis that DsbA is not necessary for Cyt c maturation and that heme ligation to apoCyt and apoCyt oxidation pathways is alternative, competing processes [84].
In gram-negative bacteria, a thioreduction pathway has evolved to specifically reduce the oxidized apoCyt substrate, Scientifica 7 which includes the Ccm proteins CcmG and CcmH. The necessary reducing power is transferred from the cytoplasmic thioredoxin (TRX) to CcmG via DsbD, a large membrane protein organized in three structural domains: an N-terminal periplasmic domain with a IgG-like fold (nDsbD), a Cterminal periplasmic domain with a thioredoxin-like (TRXlike) fold (cDsbD), and a central domain composed of eight TM helices [85]. Each of these domains contains a pair of Cys residues and transfer electrons via a cascade of disulfide exchange reactions, making DsbD a "redoxhub" in the periplasm, performing disulfide bond exchange reactions with different oxidized proteins [79]. In particular, a combination of X-ray crystallography experiments and kinetic analyses showed that electrons are transferred from the cytoplasmic TRX to the membrane domain of DsbD, followed by reduction of cDsbD and finally of nDsbD which is the direct electron donor to CcmG [85].
CcmG is a membrane-anchored protein, linked to the membrane via an N-terminal TM helix and exposing its soluble TRX-like domain in the periplasm. The 3D structure of the TRX-like domain of CcmG from different bacteria has been solved by X-ray crystallography (E. coli: PDB 1Z5Y [85]; PDB 2B1 K [86]; B. japonicum: PDB 1KNG [87]; P. aeruginosa: PDB 3KH7, 3KH9 [22]) and is generally well conserved, as proved by the low RMSD (0.8Å between Pa-CcmG and Ec-CcmG; 1.35Å between Pa-CcmG and Bj-CcmG). Although all these proteins adopt a TRX-like fold and contain the redox-active motif CXXC in the first -helix, they are inactive in the classic insulin reduction assay [75,88]; CcmG proteins are therefore considered specific thioloxidoreductase, able to recognize and selectively interact only with their upstream and downstream binding partners in the thioreduction process leading to reduced apoCytc. Looking at the 3D structure of the periplasmic domain of the prototypical Pa-CcmG, it is possible to identify the and structural motifs of the TRX fold linked by a short -helix and forming a four-stranded -sheet surrounded by three helices; the protein contains an additional N-terminal extension (residues 26-62) and a central insert (residues 102-123). The redox-active motif of Pa-CcmG (CPSC) is located in the first -helix of the TRX fold, as usually observed in all TRX-like proteins. As for any molecular machinery, where each component must recognize and interact with more than one target (i.e., the substrate and the other components of the apparatus), an open question concerns the mechanism whereby CcmG is able to recognize its different partners. The availability of the crystal structures of Pa-CcmG both in the oxidized (2.2Å resolution) and reduced state (1.8Å resolution) [22] allowed highlighting the structural similarity between the two redox states (Rmsd of the C atoms in the two redox forms is 0.19Å) and therefore to exclude structural rearrangement as the mechanism used by Pa-CcmG to discriminate between reduced (such as the nDsbD domain) and oxidized partners (Pa-CcmH and/or apoCyt).
The standard redox potential of Pa-CcmG ( 0 = 0.213 V at pH 7.0; [22], as well as that of Ec-CcmG ( 0 = 0.212 V [86]), indicates that these proteins act as mild reductants in the thioreductive pathway of Cytc biogenesis. However, the function of thiol-oxidoreductases obviously depends on the pK a values of their activesite Cys residues. The pK a of CysX (6.13 ± 0.05) and CysY (10.5 ± 0.07) are consistent with the pK a values measured in different TRXs, where the active Nterminal Cys residue has a pK a close to pH 7.0, whereas the C-terminal Cys has a much higher pK a [89,90]. Such a large difference between the two pK a values in the TRX family is functionally relevant, because it allows the N-terminal Cys to perform the nucleophilic attack on the target disulfide, while the C-terminal Cys is involved in the resolution of the resulting mixed-disulfide [90].
CcmH is the other component of System I involved in the reduction of apoCyt. Notably, CcmH proteins from different bacterial subgroups may display structural variability; indeed, while in E. coli Ec-CcmH is a bipartite protein characterized by two soluble domains exposed to the periplasm and two TM segments, CcmH from P. aeruginosa (Pa-CcmH) is a one-domain redox-active protein, anchored to the membrane via a single TM helix and homologous to the N-terminal redox-active domain of Ec-CcmH. Surprisingly, the 3D structure of the soluble periplasmic domain of Pa-CcmH revealed that it adopts a peculiar three-helix bundle fold strikingly different from that of canonical thioloxidoreductases ( Figure 5; PDB: 2HL7; [23]). The N-terminal domain of Ec-CcmH was also shown to have the same 3D structure, although helix-swapping and dimerization have been observed in this case (PDB: 2KW0; [91,92]). The conserved redox-active motif (LRCPKC) is located in the loop connecting helices 1 and 2; close to the activesite, the crystal structure reveals the presence of a small pocket on the surface of Pa-CcmH surrounded by conserved hydrophobic and polar residues, which could represent the recognition site for the heme-binding motif of apoCyt.
Concerning the functional properties of this unusual thiol-oxidoreductase, it is interesting to note that its standard redox potential ( 0 = 0.215 V) [23] Figure 6: : Alternative thioreduction pathways which may be operative in System I and hypothesized on the basis of structural and functional characterization of the redox-active Ccm proteins from P. aeruginosa [22,23,25]. Scheme 1 is a linear redox cascade whereby CcmG is the direct reductant of CcmH, which reduces oxidized apoCyt. Scheme 2 envisages a more complex scenario involving the formation of a mixeddisulfide complex between CcmH and apoCyt (Step 1). This complex is the substrate for the attack by reduced CcmG (Step 2) that liberates reduced apoCyt. The resulting disulfide bond between CcmH and CcmG is then resolved by the free Cys thiol of CcmG (probably Cys77 in Pa-CcmG). Adapted from [25].
of the TRX family, the N-terminal Cys is always solvent exposed, in CcmH proteins, the arrangement of the two Cys residues is reversed: the N-terminal Cys residue is buried, whereas the C-terminal Cys residue is solvent exposed. On the basis of this observation, it was suggested that, different from the canonical TRX redox mechanism, CcmH proteins perform the nucleophilic attack on the apoCyt disulfide via their C-terminal Cys residue [23]. This mechanism, which is in agreement with the mechanism proposed earlier for Ec-CcmH on the basis of mutational-complementation studies [93,94], is substantiated by the peculiar pK a values of the active site Cys residues of Pa-CcmH which were found to be similar for both cysteines (8.4 ± 0.1 and 8.6 ± 0.1; [23]). Again, this is different from what is generally observed in the case of TRX proteins, where the pK a value of the Cys residue performing the initial nucleophilic attack is significantly lower than the pK a value of the Cys residue responsible for the resolution of the intermediate mixed-disulfide. It is tempting to speculate that the unusual pK a values of the Pa-CcmH active site thiols may ensure the necessary specificity of this component of the Ccm apparatus toward the CXXCH motif of the apoCyt substrate.

System I: ApoCyt Thioreduction Pathway Mechanism.
Although we know that CcmG and CcmH are the redoxactive components of System I involved in the thioreductive pathway of Cyt c biogenesis, not only an accepted mechanism for the reduction of apoCyt disulfide bond is still lacking, but also the absolute requirement of such a process is now debated [38,84]. Focusing our attention on the reduction of the apoCyt internal disulfide, at least two mechanisms can been hypothesized, which involve either a linear redox cascade of disulfide exchange reactions or a nonlinear redox process involving transient formation of a mixed-disulfide complex, as depicted in Figure 6 and Schemes 1 and 2, respectively.
Both the thiol-disulfide exchange mechanisms depicted in Figure 6 suggest that CcmH is the direct reductant of the apoCytc disulfide; however, even if immunoprecipitation experiments failed to detect the formation of a mixeddisulfide complex between apoCyt and CcmH proteins [95], some in vitro evidence supporting the formation of such a complex has been presented. In particular, it has been shown that Rhodobacter capsulatus and Arabidopsis thaliana CcmH homologues (Rc-CcmH and At-CcmH) are able to reduce the CXXCH motif of an apoCyt-mimicking peptide [75,96]. In the latter case, yeast two-hybrid experiments carried out on At-CcmH, indeed revealed an interaction between the protein and a peptide mimicking the A. thaliana Cyt c sequence. In the case of Pa-CcmH, FRET kinetic experiments employing a Trp-containing fluorescent variant of the protein and a dansylated nonapeptide encompassing the heme-binding motif of P. aeruginosa cytochrome c551 (dans-KGCVACHAI) [23] allowed to directly observe the formation of the mixed-disulfide complex and to measure the off-rate constant of the bound peptide. The results of these in vitro binding experiments allowed to calculate an equilibrium dissociation constant which combines an adequate affinity (low M) with the need to release efficiently reduced apoCyt to other component(s) of the System I maturase complex [23]. More recently, the results obtained by FRET binding experiments carried out with single Cys-containing mutants of Pa-CcmH and Pa-CcmG [25] substantiated the hypothesis depicted in Scheme 2 ( Figure 6). Altogether, these structural and functional results suggest that the thioreduction pathway mechanism leading to reduced apoCyt is better described by Scheme 2 and that reducing equivalents might not be transferred directly from CcmG to apoCyt as depicted in Scheme 1. According to Scheme 2, reduced CcmH (a non-TRX-like thiol-oxidoreductase) specifically recognizes and reduces oxidized apoCyt via the formation of a mixeddisulfide complex, which is subsequently resolved by CcmG. The resulting disulfide bond between CcmH and CcmG is then resolved by the free Cys thiol of CcmG (probably Cys77 in Pa-CcmG).
However, further in vitro experiments with CcmH and apoCyt single Cys-containing mutants are needed to unveil the details of the thioreduction of oxidized apoCyt by CcmH. In particular, it would be crucial to identify the Cys residue of apoCyt that remains free in the apoCyt-CcmH mixeddisulfide complex intermediate (see Scheme 2 and Section 2.6 below) and available to thioether bond formation with one of the heme vinyl groups. Clearly, structure determination of the trapped mixed-disulfide complexes between CcmH, CcmG, and apoCyt (or apoCyt peptides) would provide key information for our understanding of this specialized thioreduction pathway mechanism.

System I: ApoCyt Chaperoning and Heme Attachment
Components. The reduced heme-binding motif of apoCyt is now available to the heme ligation reaction. However, the molecular mechanism whereby the Ccm machinery catalyzes or promotes the formation of the heme-apoCyt covalent bonds is still largely obscure, representing the most important goal in the field. Past observations and recent experiments suggest that CcmF and CcmI, possibly together with CcmH, are involved in these final steps [16,34,36].
CcmF is a large integral membrane protein of more than 600 residues, belonging to the heme handling protein family (HHP; [55]) and predicted to contain 10-15 TM helices (note that some discrepancy exists as to the number of TM helices predicted by computer programs and those predicted on the basis of phoA and lacZ fusion experiments; [40,97]), a conserved WWD domain, and a larger domain devoid of any recognizable sequence features, both exposed to the periplasm. Only recently, E. coli CcmF (Ec-CcmF) has been overexpressed, solubilized from the membrane fraction, and spectroscopically characterized in vitro [36,41]. Surprisingly, the biochemical characterization of recombinant Ec-CcmF allowed to show that the purified protein contains heme b as cofactor in a 1 : 1 stoichiometry; this observation led to the hypothesis that, in addition to its heme lyase function, Ec-CcmF may act as a heme oxidoreductase. In particular, it is possible that the heme b of Ec-CcmF may act as a reductant for the oxidized iron of the heme bound to CcmE [41]; indeed, the in vitro reduction of Ec-CcmF by quinones has been experimentally observed, strengthening the hypothesis about the quinol:heme oxidoreductase function of this elusive protein. The structural model proposed for Ec-CcmF predicts 13 TM helices and, notably, the location of the four completely conserved His residues: according to the model, two of them (His173 and His303) are located in periplasmic exposed loops next to the conserved WWD domain, which is believed to provide a platform for the heme bound to holoCcmE, while His261 is located in one of the TM helices and it is predicted to act as an axial ligand to the heme b of Ec-CcmF; the other conserved His residue (H491) could provide the second axial coordination bond to the heme, although this has not been experimentally addressed. This model of Ec-CcmF therefore envisages that this large membrane protein is characterized by two heme-binding sites: one of them is embedded in the membrane and coordinates a heme b prosthetic group necessary to reduce the CcmE-bound heme hosted in the second heme-binding site and constituted by its WWD domain.
It is interesting to note that in plants mitochondria the CcmF ortholog appears to be split into three different proteins (At-CcmFN1, At-CcmFN2 and At-CcmFC), possibly interacting each other [16]. Since each of these proteins is similar to the corresponding domain in the bacterial CcmF ortholog, this observation may provide useful information in the design of engineered fragments of bacterial CcmF proteins, amenable to structural analyses.
The other System I component, which is generally believed to be involved in the final steps of Cyt c maturation, is CcmI. As stated above, the ccmI gene is present only in some Ccm operons, while in others, the corresponding ORF is present within the ccmH gene (as in E. coli). The functional role of CcmI in Cytc biogenesis is revealed by genetic studies, showing that in R. capsulatus and B. japonicum, inactivation of the ccmI gene leads to inability to synthesize functional c-type cytochromes [98,99]. In R. capsulatus and P. aeruginosa, the CcmI protein (Rc-CcmI and Pa-CcmI, resp.) can be described as being composed of two domains, starting from the N-terminus: a first domain composed of two TM helices connected by a short cytoplasmic region and a large periplasmic domain. Structural variations may be observed among CcmI members from different bacteria; indeed, multiple sequence alignment indicates that the cytoplasmic region of Rc-CcmI contains a leucine zipper motif, which is not present in the putative cytoplasmic region of Pa-CcmI [100][101][102]. Surprisingly, no crystallographic structure is available up to now for the soluble domain of any CcmI protein, with the exception of the ortholog protein NrfG from E. coli, (Ec-NrfG) [103]. This protein is necessary to attach the heme to the unusual heme-binding motif CWSCK (where a Lys residue substitutes the conserved His) present in NrfA, a pentaheme c-type cytochrome [103,104]. According to secondary structure prediction methods [105], it has been proposed that the periplasmic domain of Pa-CcmI is composed of a N-terminal -helical region containing at least three TPR motifs connected by a disordered linker to a -C-terminal region. Multiple sequence analyses and secondary structure prediction methods show that the TPR region of Pa-CcmI can be successfully aligned with many TPR-containing proteins, including Ec-NrfG [106].

System I: ApoCyt Chaperoning and Heme Attachment
Mechanisms. TPR domain-containing proteins are common to eukaryotes, prokaryotes, and archaea; these proteins are generally involved in the assembly of multiprotein complexes and to the chaperoning of unfolded proteins [103,107]. It is therefore plausible that CcmI (or the TPR C-terminal domain of Ec-CcmH) may act to provide a platform for the unfolded apoCyt, chaperoning it to the heme attachment site, presumably located on the WWD domain of CcmF. CcmI may thus be considered a component of a membrane-integral multisubunit heme ligation complex, together with CcmF and CcmH, as experimentally observed by affinity purification experiments carried out with Rc-CcmFHI proteins [97,99,108]. According to the proposed function of CcmI, a critical requirement is represented by its ability to recognize different protein targets over and above apoCyt, such as CcmF and CcmH. However, until now, direct evidence has been presented only for the interaction of CcmI with apoCyt, but the possibility remains that CcmFHI proteins interact each other via their TM helices and not via their periplasmic domains. Interestingly, both for Pa-CcmI [106] or Rc-CcmI [99], CD spectroscopy experiments carried out on the CcmI:apoCyt complex highlighted major conformational changes at the secondary structure level. It is tempting to speculate, on the basis of these results, that in vivo the folding of apoCyt may be induced by the interaction with CcmI. In the case of P. aeruginosa System I proteins, the binding process between Pa-CcmI and its target protein, apoCyt c551 (Pa-apoCyt), has been studied both at equilibrium and kinetically [106]; the measured for this interaction (in the M range) appeared to be low enough to ensure apoCyt delivery to the other components of the Ccm machinery. Clearly, a major question concerns the molecular determinants of such recognition process; interestingly, both affinity coprecipitation assays [99] and equilibrium and kinetic binding experiments [106] highlighted the role played by the C-terminal -helix of Cyt c. Similar observations have been made for the interaction of Ec-NrfG with a peptide mimicking NrfA, its apoCyt substrate [103]; in this case, isothermal titration calorimetry (ITC) experiments indicate that the TPR-domain of NrfG serves as a binding site for the C-terminal motif of NrfA. Altogether, these observations are in agreement with the fact that TPR proteins generally bind to their targets by recognizing their C-terminal region [107].
The CcmI chaperoning activity has been experimentally supported for the first time in the case of Pa-CcmI by citrate synthase tests [106]: it has been proposed that the observed ability to suppress protein aggregation in vitro may reflect the capacity of CcmI to avoid apoCyt aggregation in vivo. Still another piece of the Cyt c biogenesis puzzle has been added recently by showing that Rc-CcmI is able to interact with apoCcmE, either alone or together with its substrate apoCyt c2, forming a stable ternary complex in the absence of heme [109]. This unexpected observation, obtained by reciprocal copurification experiments, provides supporting evidence for the existence of a large multisubunit complex composed of CcmFHI and CcmE, possibly interacting with the CcmABCD complex. It is interesting to note that, while in the case of the CcmI:apoCyt recognition different studies highlighted the crucial role of the C-terminal helical region of apoCyt (see above), in the case of the apoCcmE: apoCyt recognition, the N-terminal region of apoCyt seems to represent a critical region.
It is generally accepted that CcmF is the Ccm component responsible for heme covalent attachment to apoCyt; however, as discussed above, it is possible that this large membrane protein plays such a role only together with other Ccm proteins such as CcmH and CcmI. Moreover, as recently discovered by Kranz and coworkers [36,41], CcmF may also act as a quinole:heme oxidoreductase, ensuring the necessary reduction of the oxidized heme b bound to CcmE. Why it is necessary that the heme iron be in its reduced state rather than in its oxidized state is not completely clear, although it is possible that this is a prerequisite to the mechanism of thioether bond formation [110]. According to current hypotheses, it is likely that the periplasmic WWD domain of CcmF provides a platform for heme b binding. Sanders et al. and Verissimo et al. [34,109] have presented a mechanistic view of the heme attachment process, which takes into account all the available experimental observations on the different Ccm proteins. According to this model, stereospecific heme ligation to reduced apoCyt occurs because only the vinyl-4 group is available to form the first thioether bond with a free cysteine at the apoCyt heme-binding motif, since the vinyl-2 group is involved (at least in the Ec-CcmE) in the covalent bond with His130 of CcmE [67]. However, experimental proof for this hypothesis requires a detailed investigation of the apoCyt thioreduction process catalyzed by CcmH (see Section 2.4).
It should be noticed that the mechanisms described so far for the function(s) played by CcmF (see [34,36,109]) do not envisage a clear role for its large C-terminal periplasmic domain (residues 510 to 611 in Ec-CcmF). It would be interesting to see if this domain, apparently devoid of recognizable sequence features, may mediate intermolecular recognition processes with one (or more) component(s) involved in the heme:apoCyt ligation process.

System II
System II is typically found in gram-positive bacteria and in in -proteobacteria; it is also present in most -and some -proteobacteria, in Aquificales and cyanobacteria, as well as in algal and plant chloroplasts. System II is composed of three or four membrane-bound proteins: CcdA, ResA, CcsA (also known as ResC), and CcsB (also known as ResB) (Figure 3). CcdA and ResA are redox-active proteins involved in the reduction of the disulfide bond in the heme-binding motif of apoCyt, whereas CcsA and CcsB are responsible for the heme-apoCyt ligation process and are considered Cyt c synthethases (CCS). Both CcsA, which is evolutionary related to the CcmC and CcmF proteins of System I [55], and CcsB are integral membrane proteins. In some -proteobacteria, such as Helicobacter hepaticus and Helicobacter pylori, a single fusion protein composed of CcsA and CcsB polypeptides is present [41,111]. Although, as discussed below, evidence has been put forward to support the hypothesis that the CcsBA complex acts a heme translocase, we still do not know if the heme is transported across the membrane by component(s) of System II itself or by a different, unidentified process.

System II: ApoCyt Thioreduction Pathway.
After the Sec machinery secretes the newly synthesized apoCyt, it readily becomes a substrate for the oxidative system present on the outer surface of the cytoplasmic membrane of the grampositive bacteria. In B. subtilis, the BdbCD system [112,113] is functionally, but not structurally, equivalent to the well-characterized DsbAB system present in gram-negative bacteria. As discussed above for System I, the disulfide of the apoCyt heme-binding motif must be reduced in order to allow thioether bonds formation and heme attachment. ResA is the extracytoplasmic membrane-anchored TRX-like protein involved in the specific reduction of the apoCyt disulfide bond; after the disulfide bond exchange reaction has occurred, oxidized ResA is reduced by CcdA which receives its reducing equivalents from a cytoplasmic TRX [114]. Although ResA displays a classical TRX-like fold, the analysis of the 3D structure of oxidized and reduced ResA from B. subtilis (Bs-ResA) showed redox-dependent conformational modifications not observed in other TRXlike proteins. Interestingly, such modifications occur at the level of a cavity proposed to represent the binding site for oxidized apoCyt [24,115,116]. Another peculiar feature of Bs-ResA is represented by the unusually similar pK a values of its the active site Cys residues (8.8 and 8.2, resp.), as observed also in the case of the active site Cys residues of the System I Pa-CcmH (see Section 2.3). However, at variance with Pa-CcmH, in Bs-ResA, the large separation between the two cysteine thiols observed in the structure of the reduced form of the protein can be invoked to account for this result.
CcdA is a large membrane protein containing six TM helices [117,118], homologous to the TM domain of E. coli DsbD [85,119]. Its role in the Cyt c biogenesis is supported by the observation that inactivation of CcdA blocks the production of c-type cytochromes in B. subtilis [120,121]. Moreover, over and above the reduction of its apoCyt substrate, Bs-CcdA is able to reduce the disulfide bond of other secreted proteins, such as StoA [122]. It is interesting to note that ResA and CcdA are not essential for Cyt c synthesis in the absence of BdbD or BdbC or if a disulfide reductant is present in the growth medium [123,124]. As discussed above (Section 2.4), a similar observation was made on the role of the thio-reductive pathway of System I: in this case, persistent production of c-type cytochromes was observed in Dsb-inactivated bacterial strains [38]. Following these observations, the question has been put forward as to why the Cyt c biogenesis process involves this apparently redundant thio-reduction route only to correct the effects of Bdb or Dsb activity. Referring to the case of B. subtilis [111], it has been proposed that the main reason is that BdbD must efficiently oxidize newly secreted proteins, since the activity of most of them depends on the presence of disulfide bonds. Alternatively, it can be hypothesized that the intramolecular disulfide bond of apoCyt protects the protein from proteolytic degradation or aggregation, or from cross-linking to other thiol-containing proteins.

System II: Heme Translocation and Attachment to ApoCyt.
Recent experimental evidence is accumulating supporting the involvement of the heterodimeric membrane complex ResBC, or of the fusion protein CcsBA, in the translocation of heme from the n-side to the p-side of the bacterial membrane. In particular, it has been shown that CcsBA from H. hepaticus (Hh-CcsBA) is able to reconstitute Cyt c biogenesis in the periplasm of E. coli [36]. Moreover, it was also observed that Hh-CcsBA is able to bind reduced heme via two conserved histidines flanking the WWD domain and required both for the translocation of the heme and for the synthetase function of Hh-CcsBA [36]. A different study carried out on B. subtilis System II proteins provided support for heme-binding capability by the ResBC complex; according to the results obtained on recombinant ResBC, the ResB component of the heterodimeric CCS complex is able to covalently bind the heme in the cytoplasm (probably by a Cys residue) and to deliver it to an extracytoplamic domain of ResC, which is responsible for the covalent ligation to apoCyt [117]. It should be noticed, however, that the transfer of the CCS-bound heme to apoCyt still awaits direct experimental proof. Moreover, it has also been reported that in B. subtilis, the inactivation of CCS does not affect the presence of other heme-containing proteins in the periplasm, such as cytochrome b562 [111]; this observation, which is in contrast to the heme-transport hypothesis by CCSs, parallels similar concerns about heme translocation mechanism that are currently discussed in the context of System I (see Section 2.2 above). In the case of the Hh-CcsBA synthetase, site-directed mutagenesis experiments allowed to assign a heme-binding role for the two pairs of conserved His residues; according to the topological model of the protein obtained by alkaline phosphatase (PhoA) assays and GFP fusions, the conserved His77 and His858 residues are located on TM helices, while His761 and His897 are located on the periplasmic side [36]. These observations, together with the results of site-directed mutagenesis experiments, allowed the authors to suggest that His77 and His858 form a low affinity-membrane embedded, heme-binding site for ferrous heme which is subsequently translocated to an external heme-binding domain of Hh-CcsBA, where it is coordinated by His761 and His897. The topological model, therefore, predicts that this last His pair is part of a periplasmic-located WWD domain (homologous to the WWD domains found in the CcmC and CcmF proteins of System I described above).

System III
Strikingly different from Systems I and II, the Cyt c maturation apparatus found in fungi and in metazoan cells (System III) is composed of a single protein, known as Holo-Cytochrome c Synthetase (HCCS) or Cytochrome c Heme Lyase (CCHL), apparently responsible for all the subprocesses described above (heme transport and chaperoning, reduction and chaperoning of apoCyt, and catalysis of the thioether bonds formation between heme and apoCyt) ( Figure 4). Surprisingly, although this protein has been identified in S. cerevisiae mitochondria several years ago [125,126], only very recently the human HCCS has been expressed as a recombinant protein in E. coli and spectroscopically characterized in vitro [127]. It is worth noticing that human HCCS is attracting interest since, over and above its role in Cyt c biogenesis, it is involved in diseases such as microphthalmia with linear skin defects syndrome (MLS), an X-linked genetic disorder [128][129][130] and in other processes, such as Cytc-independent apoptosis in injured motor neurons [131]. Different from animal cells, where a single HCCS is sufficient for the maturation of both soluble and membrane-anchored Cytc (Cyt c and Cy c1, resp.), in S. cerevisiae two homologs, HCCS and HCC1S located in the inner mitochondrial membrane and facing to the IMS space [132,133] are responsible for heme attachment to apoCyt c and apoCyt c1, respectively [125,134]. It should also be noticed that in fungi, an additional FADcontaining protein (Cyc2p) is required for Cyt c synthesis. Cyc2p is a mitochondrial membrane-anchored flavoprotein exposing its redox domain to the IMS, which is required for the maturation of Cyt c but not for that of Cyt c1 [135]. This protein does not contain the conserved Cys residues typically found in disulfide reductases and indeed it is not able to reduce oxidized apoCyt in vitro. However, it has been recently shown that Cyc2p is able to catalyze the NAD(P)Hdependent reduction of heme in vitro [136], a necessary step before the thioether bond formation can occur, as discussed above (see Section 2.6). This result, together with the observation that Cyc2p interacts with HCCS and with apoCyt c and c1 lends support to the proposal that Cyc2p is involved in the reduction of the heme iron in vivo [136,137].
Although HCCS proteins are crucial for Cyt c maturation, we still do not know how these proteins recognize their substrates (heme and apoCyt) and how they promote or catalyze the formation of thioether bonds between the heme vinyl groups and the cysteine thiols of the apoCyt CXXCH motif.
Contrary to the broad specificity of System I, which is able to recognize and attach the heme to prokaryotic and eukaryotic c-type cytochromes [49,50], and even to very short microperoxidase-like sequences [49,50], mitochondrial HCCS is characterized by a higher specificity, as it does not recognize bacterial apoCyt sequences. These observations prompted the investigation of the recognition process between apoCyt and HCCS. Recently, by using a recombinant yeast HCCS and chimerical apoCyt sequences expressed in E. coli, it was possible to conclude that a crucial recognition determinant is represented by the N-terminal region of apoCyt containing the heme-binding motif [35]; notice that, in the context of System I, the same N-terminal region of the Cyt c sequence has been recently identified to be important for the recognition by apoCcmE (see Section 2.6). Over and above the role played by the intervening residues in the CXXCH heme-binding motif [135], it has been shown that a conserved Phe residue, occurring in the N-terminal region before the CXXCH motif, is important for HCCS recognition [35,138]. These results support the hypothesis that this residue, known to be a key determinant of Cytc folding and stability [19,20,139], may also be crucial for Cytc maturation by HCCS.
Another relevant question concerns the ability of HCCS to recognize and bind the heme molecule, as the region of the protein responsible for heme recognition remains to be identified. Initially, it was hypothesized that the recognition of heme could be mediated by the CP motifs present in the HCCS protein [140]; these short sequences are indeed known to bind heme in a variety of heme-containing proteins [141,142]. However, it has been recently shown that CP motifs of the recombinant S. cerevisiae HCCS are not necessary for Cyt c production in E. coli [143], excluding them as key determinants of heme recognition.
The long-awaited in vitro characterization of the recombinant human HCCS allowed for the first time to propose a molecular mechanism underlying Cytc maturation in eukaryotes which can be experimentally tested [127]. According to the proposed model, the human HCCS activity can be described as a four step mechanism, involving (i) heme-binding, (ii) apoCyt recognition, (iii) thioether bonds formation, and (iv) holoCyt c release. In particular, the heme is proposed to play the role of a scaffolding molecule, mediating the contacts between HCCS and apoCyt. Mutagenesis experiments carried out on the recombinant HCCS strongly suggest that heme-binding (Step 1) depends on the presence of a specific His residue (His154), acting as an axial ligand to ferrous heme. Residues present at the Nterminus of apoCyt mediate the recognition with HCCS (Step 2); as discussed above, it is known that this region forms structurally conserved -helix in the fold of all ctype cytochromes. Unfortunately, no information is available up to now concerning the region of HCCS involved in the recognition and binding to the N-terminal region of apoCyt. Coordination of the heme iron by the His residue of the apoCyt heme-binding motif CXXCH provides the second axial ligand to the heme iron and is probably important for the correct positioning of the two apoCyt Cys residues and formation of the thioether bonds (Step 3). The final release of functional Cyt c (Step 4) clearly requires the displacement of the His154:Fe 2+ coordination bond; such a displacement is probably mediated by formation of the coordination bond with the Cyt c conserved Met residue and/or by the simultaneous folding of Cyt c. Again, it is interesting to note that this last hypothesis is in accordance with in vitro folding studies on c-type cytochromes that highlighted the late formation of the Met-Fe coordination during Cyt c folding [144,145].