Improved Recovery and Identification of Membrane Proteins from Rat Hepatic Cells using a Centrifugal Proteomic Reactor*

Despite their importance in many biological processes, membrane proteins are underrepresented in proteomic analysis because of their poor solubility (hydrophobicity) and often low abundance. We describe a novel approach for the identification of plasma membrane proteins and intracellular microsomal proteins that combines membrane fractionation, a centrifugal proteomic reactor for streamlined protein extraction, protein digestion and fractionation by centrifugation, and high performance liquid chromatography-electrospray ionization-tandem MS. The performance of this approach was illustrated for the study of the proteome of ER and Golgi microsomal membranes in rat hepatic cells. The centrifugal proteomic reactor identified 945 plasma membrane proteins and 955 microsomal membrane proteins, of which 63 and 47% were predicted as bona fide membrane proteins, respectively. Among these proteins, >800 proteins were undetectable by the conventional in-gel digestion approach. The majority of the membrane proteins only identified by the centrifugal proteomic reactor were proteins with ≥2 transmembrane segments or proteins with high molecular mass (e.g. >150 kDa) and hydrophobicity. The improved proteomic reactor allowed the detection of a group of endocytic and/or signaling receptor proteins on the plasma membrane, as well as apolipoproteins and glycerolipid synthesis enzymes that play a role in the assembly and secretion of apolipoprotein B100-containing very low density lipoproteins. Thus, the centrifugal proteomic reactor offers a new analytical tool for structure and function studies of membrane proteins involved in lipid and lipoprotein metabolism.

Membrane proteins play an important role in a variety of cellular functions, ranging from signal transduction, subcellular compartmentalization, membrane trafficking, and protein secretion, in addition to their function in providing and maintaining the structural integrity of membranes. Not surprisingly, the membrane associated proteins account for nearly 60% of pharmaceutical drug targets (1)(2)(3). Depending upon the physical nature of interactions between proteins and membranes, membrane proteins are broadly classified as integral membrane proteins (proteins that contain hydrophobic transmembrane segments in their sequences) and peripheral membrane proteins. Although the peripheral membrane proteins are in general soluble and relatively amiable for identification using proteomic approaches, integral membrane proteins pose greater challenges owing to low abundance and hydrophobicity (4,5).
Many analytical approaches and strategies have been developed to facilitate membrane protein characterization. The low abundance issue has been addressed by enriching samples using subcellular fractionation, (e.g. sucrose or sorbitol density ultracentrifugation) (6 -9), cationic colloidal silica absorption (10), aqueous-polymer two-phase system (11), and triton X-114 phase separation (12). In addition, high abundant nonmembrane proteins can be separated from membrane proteins by using high-salt and high-pH buffers (13,14). The hydrophobicity issue of membrane proteins has been circumvented by the use of mass spectrometry compatible surfactants (15), organic solvents (60% methanol) (16), and multiple enzymes (17,18). Most of these approaches have been applied to analyze plasma membrane and integral membrane proteins (6,13,14,19,20). However, studies with microsomal membranes using proteomic approach are relatively limited (21,22).
The microsomal membranes, composed of endoplasmic reticulum (ER) 1 and Golgi apparatus, represent the cellular compartments where synthesis, post-translational modification, assembly, and secretion of various proteins and lipoproteins occur. In hepatic cells, the ER and Golgi microsomes play a major role in the assembly and secretion of very low density lipoproteins (VLDL) rich in triglycerides (TAG) and cholesterol (23)(24)(25)(26)(27). Multiple protein factors are required for the process of hepatic VLDL assembly and secretion, of which apolipoprotein (apo) B-100, an extremely large (4536 amino acids) and hydrophobic protein serves as a structural backbone in TAG recruitment during the VLDL assembly process. Another protein, termed microsomal triglyceridetransfer protein (MTP) that is encoded by the abetalipoprotein gene MTTP, is a microsome-resident protein that plays an obligatory role in facilitating VLDL assembly and secretion (25). Expression of other proteins, such as the low density lipoprotein (LDL) receptor, also influences the VLDL assembly and secretion process by regulating degradation of apoB-100 (28). The recruitment of lipids in VLDL assembly starts immediately during and after apoB-100 translation and translocation across the ER membrane (29). However, microsomal membrane proteins that may play a role in the initial VLDL assembly process that occurs in association with membranes are not fully characterized.
The purpose of the current work is to determine the proteome of ER and Golgi microsomal membranes in hepatic cells. Recently, we have developed a microfluidic device, termed the proteomic reactor, for rapid preconcentration, derivatization, and enzymatic digestion (30). This proteomic reactor has been successfully applied to the analysis of complex protein mixtures (31)(32)(33) and post-translational modifications (34 -36). Moreover, a multiplexed proteomic reactor has been developed for parallel processing of minute amounts of protein sample (37). In this study, we developed a simplified reactor compatible with bench-top centrifuges. The centrifugal proteomic reactor allowed improved recovery as well as identification of microsomal membrane proteins from the rat hepatoma cell line McA-RH7777. The centrifugal proteomic reactor identified 945 plasma membrane proteins and 955 microsomal membrane proteins with respectively 63 and 47% predicted as bona fide membrane proteins. Among these proteins, Ͼ800 proteins were undetectable by the conventional in-gel digestion approach.
Cell Culture-The rat hepatoma McA-RH7777 cells were cultured in Dulbecco's modified Eagle's medium supplemented with 10% fetal bovine serum and 10% horse serum as described previously (38).
Plasma and Microsomal Membrane Isolation-The flowchart of membrane preparation is shown in Fig. 1. Cells at 80% confluence (5 ϫ 10 6 cells were plated in 10-cm dish) cultured in the Dulbecco's modified Eagle's medium containing 20% fetal bovine serum were washed with ice-cold phosphate-buffered saline three times. Total of four dishes of cells were collected into homogenization buffer (20 mM Tris-HCl, pH 7.4, 250 mM sucrose, 1 mM EDTA, and protease inhibitor mixture), and homogenized by 20 passes through a ball bearing homogenizer (H and Y Enterprise, Redwood City, CA) (Step 1 in Fig.  1A). The homogenates were centrifuged (11,000 ϫ g, 10 min, 4°C) to pellet nucleus, mitochondria, plasma membrane, and unbroken cells (Step 2). The post-nuclear supernatant was centrifuged (541,000 ϫ g, 16 min, 4°C) to recover the microsome (Step 3a), whereas the pellet was resuspended in the homogenization buffer (devoid of sucrose) using a glass homogenizer, layered onto a 1.12 M sucrose cushion, and centrifuged (100,000 ϫ g, 90 min, 4°C) to sediment plasma membrane at the interface (Step 3b). The respective plasma and microsomal membranes (obtained from 3a and 3b) were subjected to two additional washing steps, namely high pH (sodium carbonate 100 mM, pH 11.0; Step 4) and 4 M Urea (20 mM Tris-HCl pH7.4, 1 mM EDTA, protease inhibitor mixture; Step 5), in an attempt to remove loosely associated peripheral membrane proteins.
Centrifugal Proteomic Reactor-The flowchart for the centrifugal reactor procedures is shown in Fig. 1D. Briefly, 20 g of plasma or microsomal membrane protein was solubilized using an extraction buffer containing 50% methanol, 2 M urea and 2% CHAPS, and the samples were transferred into 1.5 ml Eppendorf tubes (Step 1 in Fig.  1D), mixed with 10 l of strong cation exchange slurry in the presence of 1.2 ml of 50% methanol and 5% formic acid by vigorous vortexing (for 1 min) (Step 2). The samples were centrifuged (16,100 ϫ g, 2 min), and the pellet was again treated with 1.2 ml 0.5% formic acid (Step 3). The samples were reduced by mixing with 20 l of 150 mM NH 4 HCO 3 , 20 mM DTT (shaking at 800 rpm, 56°C, 15 min), and after reduction the dithiothreitol in the sample was diluted using 1.2 ml 0.5% formic acid and followed by centrifugation (Step 4). The samples were then subjected to alkylation by mixing with 20 l of 150 mM NH 4 HCO 3 , 100 mM iodoacetamide in darkness (15 min, room temperature), and the reaction was stopped by adding 1.2 ml of 0.5% formic acid containing 2 g trypsin (Step 5). After centrifugation, the resulting pellet was dissolved in 20 l of 1 M NH 4 HCO 3 , and followed by trypsin digestion on a shaker at 800 rpm at 37°C for 2 h (Step 6). Finally, 1.2 ml of 5% formic acid was added to elute the pH 2.5 fraction by centrifugation, followed by additional nine pH fractions (pH 3.0, 3.5, 4.0, 4.5, 5.0, 5.5, 6.0, 8.0, 12) with 300 l of respective pH buffers (Step 7) (39). The fractionated samples were subjected to liquid chromatography-tandem MS (LC-MS/MS) analysis (Step 8).
After the desalting step, the flow was split, and peptides were eluted through a second 75 m ϫ 150 mm column packed with 3-m C18 beads at ϳ150 nL/min. The peptides were eluted using a gradient (5-80% acetonitrile with 0.1% formic acid) over a 2 h period into an ESI linear trap quadrupole (LTQ)-Orbitrap mass spectrometer (Thermo Electron, Waltham, MA). MS/MS spectra were acquired in a data-dependent acquisition mode that automatically selected and fragmented the 10 most intense peaks from each MS spectrum generated.
In-gel Digestion-Protein samples (20 g) were dried, reconstituted in gel loading buffer and separated by polyacrylamide gel electrophoresis in the presence of SDS (SDS-PAGE) (4ϳ12% NuPAGE gel) at a constant voltage setting of 80 V for 30 min and then 120 V thereafter until the bromphenol blue dye marker reached the bottom of the gel. Proteins were visualized using colloidal blue staining (Invitrogen, Carlsbad, CA), and the gels were sliced into ten pieces of equal length and the in-gel digestion was performed as reported previously (40).
Data Analysis-Maxquant (41) (http://maxquant.org/, version 1.0. 13.13) was used to generate peak lists from raw files, and Mascot (version 2.2.02 Matrix Science, London, UK) was used to search the protein sequence database using the following parameters: carbamidomethyl (C) was set as a fixed modification, whereas oxidation (M, ϩ15.99492 Da) was set as a variable modification. Acquired MS/MS spectra were searched against the decoyed rat International Protein Index protein sequence database (version 3.52, 39,906 protein sequences; European Bioinformatics Institute) augmented with the reversed sequence of each entry in the forward database. The precursor and fragment mass tolerances for the searching were set at 7 ppm and 0.5 Da, respectively. Trypsin was selected as the digestive enzyme with two potential missed cleavages. Only fully tryptic peptides ranked first were accepted in our database searching results. The false positive rate was controlled at Ͻ1% using the equation false positive rate ϭ # of false peptides/(# of true peptides ϩ # of false peptides) ϫ 100. The proteins with at least two unique peptides were accepted for following analysis. The mascot cut-off score is 24 for both reactor and in-gel digestion data sets. Membrane protein prediction was achieved using the DAVID Bioinformatics Resources (http://david.abcc.ncifcrf.gov/)(42) and the Gene Ontology (GO) annotation (www.geneontology.org) and the TransMembrane Hidden Markov Model (TMHMM, http://www.cbs.dtu.dk/services/TMHMM/). We used PANTHER (http://www.pantherdb.org/) to do the biological process annotation. The protein sequence comparison between this study and others was performed using Protein Mapping and Comparison Tool (PROMT, http://www.geneinfo.eu/prompt/), and the two protein sequences with Ͼ ϭ 80% identity were consider as overlapped proteins. Maxquant (41) (version 1.1.1.36) was used for label-free quantitation of the proteins from in-gel and on-reactor digestion.

Plasma and Microsomal
Membrane Preparation-We developed a method that combines membrane fractionation, a centrifugal proteomic reactor, and HPLC-ESI-MS/MS to study membrane proteins with a particular focus on plasma and microsomal membranes. This method consists of first separating plasma and microsomal membranes through multistep centrifugations (Fig. 1A). The proteins from the plasma and microsomal membranes were captured and processed on a centrifugal proteomic reactor prior to analysis by HPLC-ESI-MS/MS. In contrast to our previously reported proteomic reactor for minute amounts of sample, the centrifugal proteomic reactor was constructed in such a way that the amount of samples to be processed can be scaled up to hundreds of micrograms. In addition, all of the processing steps involved centrifugation that effectively minimized sample loss during multiple washing steps (see Experimental Procedures for details). As a proof-of-principle, we compared the results obtained from the membrane enrichment method followed by either the centrifugal proteomic reactor or conventional SDS-PAGE and in-gel digestion method. Plasma and microsomal membranes were isolated from the rat hepatoma McA-RH7777 cells, a cell line that has been used extensively in the studies of hepatic TAG-rich lipoprotein assembly and secretion (43). Approximately 100 g proteins were obtained from respective plasma and microsomal membrane samples derived from four 10-cm dishes of cells (total of about 20 mg cells proteins) using the protocol depicted in Fig. 1A. Staining of SDS-PAGE resolved protein samples derived from equal amounts of cell lysate, plasma membranes, and microsomal membranes, respectively, showed noticeable difference in protein banding patterns (Fig. 1B). Western blot analysis showed (Fig. 1C) that calnexin (an ER membrane protein) was enriched in both plasma and microsomal membrane fractions as compared with that in cell lysate, whereas actin beta (actb, a cytoplasmic protein) and lamin A/C (a nuclear membrane protein) were not detected in these samples. Thus, contamination of plasma or microsomal membranes by cytosol or nucleus was minimal.
Process of Membrane Proteins with the Centrifugal Reactor-Plasma and microsomal membrane proteins obtained above were processed by the centrifugal proteomic reactor prior to LC-MS/MS analysis (Fig. 1D), and the results were contrasted with those derived from conventional in-gel digestion methodology (Fig. 2). There are 62,958 peptides (4651 unique peptides) and 101,794 peptides (5577 unique peptides), resulting in 945 and 955 proteins identified by centrifugal proteomic reactor from plasma and microsomal membranes, respectively; whereas there are only 9843 peptides (297 unique peptides) and 9947 peptides (397 unique peptides), resulting in 110 and 128 proteins identified by conventional in-gel digestion from plasma and microsomal membranes, respectively (Table I, supplemental Table S4). Notably, greater than 95% of membrane proteins detected by the in-gel method were also identified by the reactor approach, authenticating the efficacy of the centrifugal reactor (supplemental Table S1). Moreover, the centrifugal proteomic reactor method exhibited less contamination by cytosolic pro-teins. For instance, actin (actb), identified in plasma and microsomal membranes by in-gel digestion, was not seen either by Western blot or by the centrifugal proteomic reactor. The heatmaps were generated to compare the identified proteins between on-reactor digestion and in-gel digestion using peptide hits and peak intensities from label-free quantitation (supplemental Fig. S6). The patterns of the heatmap from peptide hits and peak intensities were similar to each other. Furthermore, some proteins not identified by MS/MS (no peptide hits because of low quantity) from in-gel digestion were still present in the MS scans and quantified by peak intensity from label-free quantitation.
The plasma and microsomal membrane fractions obtained were enriched for authentic membrane proteins. The DAVID Bioinformatics Resources suggested that of all proteins identified in the plasma and microsomal membranes, ϳ50 -60% were bona fide membrane proteins and ϳ30 -50% were integral membrane proteins, regardless whether the processing was done by in-gel digestion or proteomic reactor method (Table I). Additional analysis using the TMHMM software suggested that ϳ40 -50% of the identified membrane proteins contained transmembrane domain(s) ( Table I). There was considerable overlap (59% of total proteins identified) between plasma and microsomal membrane fractions (supplemental Fig. S1). However, clear distinctions in protein composition did occur between the two fractions. Thus, of total proteins identified, 20% were found only in the plasma membranes, whereas 21% were found only in the microsomal membranes. The percentage of bona fide membrane proteins predicted by the DAVID bioinformatics resources also showed a distinction between the two fractions; whereas 77% in plasma membrane fraction were membrane proteins, the number for microsomal membrane fraction was only 16%. The nonintegral membrane proteins associated with the microsomal membrane fraction were mostly ribosome-and proteasome-related proteins that are involved in protein synthesis and degradation (supplemental Table S1B). Apparently, these proteins are abundant and bind tightly to the microsomal membrane even after high pH and 4 M urea wash. The membrane proteins involved in lipid metabolism and in ER and Golgi trafficking were identified exclusively in the microsomal membrane fraction and not in the plasma membrane fraction. The membrane proteins related to lipid metabolism included elongation of very long chain fatty acids protein 5 (Elovl5, lipid synthesis), lysophosphatidylglycerol acyltransferase 1 (LOC683760, lipid synthesis), solute carrier family 27 (fatty acid transporter), member 6 (Slc27a6, lipid transporting), arylacetamide deacetylase-like 1 (Aadacl1, lipid hydrolysis), and cytochrome P450 2D4 (Cyp2d4v1, lipid oxidation). The membrane proteins involved in ER and Golgi trafficking included ERGIC and golgi 3 (Ergic3), sec1 family domain-containing protein 1 (Scfd1), isoform 1 of protein YIF1B (Yif1b), coatomer subunit beta (Copb1), AP-2 complex subunit mu-1 (Ap2m1). On the other hand, membrane proteins detected exclusively in the plasma membrane fraction (and not in the microsomal membrane fraction) included ATPase and transporters, such as copper-transporting ATPase 1 (Atp7a), isoform D of plasma membrane calcium-transporting ATPase 1 (Atp2b1), sodium and hydrogen exchanger 1 (Slc9a1), sulfate anion transporter 1 (Slc26a1), similar to solute carrier family 37 (glycerol-3-phosphate transporter), member 2 (Slc37a2), sodium-and chloride-dependent glycine transporter 1 (Slc6a9), and chloride channel protein 5 and 7 (Clcn5, Clcn7), to name a few.
Membrane proteins that were only identified by the centrifugal proteomic reactor covered a broad spectrum of functions, ranging from cell communication, adhesion, apoptosis, energy, and intermediate metabolism (Fig. 2). Detailed analysis was performed to determine if the membrane proteins that were only identified by the centrifugal proteomic reactor method had particular characteristics such as size (MW), hydrophobicity (GRAVY), isoelectric point (pI), or the presence of transmembrane (TM) segments. As shown in Fig. 3A, among 110 proteins identified by in-gel digestion in plasma membranes, only 10 (9%) had MW Ͼ100 kDa and 14 (13%) with GRAVY Ͼ 0. The largest MW and GRAVY values identified by in-gel method were 251 kDa and 0.82, respectively. In comparison, the reactor approach identified 123 (15%) proteins with MW Ͼ100 kDa and 199 (24%) proteins with GRAVY Ͼ 0. The largest MW and GRAVY values identified by reactor approach were 3704 kDa and 1.10, respectively (supplemental Fig. S2A and S2B). Likewise, proteins with high MW  and GRAVY values were detected by the reactor approach for microsomal membrane samples (Fig. 3B). These data indicate that the centrifugal proteomic reactor can identify the vast majority of the proteins observed by in gel digestion, but moreover can detect membrane proteins with high MW and hydrophobicity.
With respect to the number of TM segments, only 13 out of total 110 plasma membrane proteins (12%) identified by in-gel digestion had TMs Ն 2. Whereas of total 840 proteins from plasma membrane identified only by the centrifugal proteomic reactor, 247 (29%) had TMs Ն 2 (Fig. 3C). Sim-ilarly, detection of the proportion of microsomal membrane proteins having TMs Ն 2 were increased from 13% by in-gel digestion method to 23% by the reactor approach (Fig. 3D). Thus, the majority of membrane proteins that failed to be detected by the in-gel digestion method were those proteins that contain two or more TM segments. Notably, the proteins with highest transmembrane domains (16 TMs), isoform 1 of multidrug resistance-associated protein 1 (Abcc1) and ATP-binding cassette, subfamily C (CFTR/MRP), member 3 (Abcc3), were only identified by the centrifugal reactor approach (supplemental Fig. S2C and S2D), which are involved in transporting various molecules across extra-and intra-cellular membranes. Another multiple transmembrane spanner protein involved in lipoprotein metabolism, the ATBbinding cassette A1 (Abca1, with 13 TMs predicted by TMHMM software), was also only detected by the reactor approach (supplemental Table S2). On the contrary, pI values (ranging from 4 to 12) of membrane proteins did not appear to have an impact on the recovery between the in-gel digestion and the reactor approach (Figs. 3C and 3D).
Microsomal Membrane Protein Analysis-The ER and Golgi microsomes in hepatic cells act as a cradle for the assembly and secretion of VLDL. Each VLDL particle is composed of a single copy of apoB-100 and various amounts of lipids (such as phospholipids, TAG and cholesterol). Although apoB-100 does not contain any TM segments, the protein has been found in close association with ER microsomal membranes. It has been postulated that the association of apoB-100 with ER membrane represents the initial stage of lipid recruitment during VLDL assembly. Hence, we examined closely the microsomal membrane proteins identified between the in-gel digestion and the reactor methods. It was reported previously that there are 17 proteins interacting with apoB-100 as determined by in vivo and in vitro screening (www.hprd.org). The reactor approach identified 12 of the 17 proteins whereas the in-gel digestion method only detected four (Fig. 4A). The identified apoB-100 interactors included MTP (Mttp) and LDL receptor (Ldlr), which play key roles in apoB-100 lipidation and degradation processes (28,44). Both of the proteins were detected only by the reactor approach and were missed by the in-gel digestion method. Other proteins that interacted with apoB-100 within the microsomes include molecular chaperones that play a role in apoB-100 folding (e.g. calnexin, calreticulin, GRP78/BiP, and protein disulfide isomerise) ( Table II). Association of these chaperone proteins with apoB-100 has been observed previously by cross-linking experiments in hepatic cells (45). Hepatic lipase (Lipc), megalin (Lrp2), apoA-I (Apoa1), and two other proteins that were reported to interact with apoB-100 were not detected in the current study, suggesting that these proteins may not interact with membrane-associated apoB-100 during VLDL assembly, or are present in McA-RH7777 cells at low abundance.
Plasma Membrane Protein Analysis-Finally, we analyzed proteins associated with plasma membranes, particularly proteins with receptor function ranging from signaling, endocytosis, virus entrance, transport, and trafficking, and others (Fig. 4B). Of note, most of these receptor proteins failed to be detected by the in-gel method, among them several play important roles in lipoprotein metabolism, such as LDL receptor (Ldlr), lipolysis stimulated lipoprotein receptor (Lsr), scavenger receptor B1 (Scarb1), and LDL receptor-related protein 1 (Lrp1) (supplemental Table S3). Additionally, the important receptors for signaling transduction, such as tumor necrosis factor (TGF) receptor type 2, epidermal growth factor receptor and insulin receptor, were exclusively detected by centrifugal reactor (supplemental Table S3).

Development of Centrifugal Proteomic
Reactor-The centrifugal proteomic reactor described in the current study has several operational advantages over the previously described column-based proteomic reactor (30,(32)(33)(34)(35)(36)39). First, because all the processing steps, including delipidation, acidification, reduction, alkylation, digestion, and pH gradient elution, were conducted with proteins absorbed onto the SCX beads, the quantity of protein sample loading could be scaled up to hundreds of micrograms. Second, because the transition between each step was achieved by simple centrifugations, the entire process prior to LC-MS/MS could be accomplished in 2 1 ⁄2 hours. Third, the bench-top microfuge-based proteomic reactor eliminated the need for specialized equipment allowing the procedure to be performed in any proteomic laboratory. Using this centrifugal proteomic reactor, we were able to identify over 900 proteins associated with plasma or microsomal membranes from 20 g starting materials, which was eight times more than the number of proteins identified by our conventional in-gel digestion method. The in-gel digestion method conducted in the current study and reported previously yielded as low as 2.22 (47) or 0.65 (19) transmembrane proteins per microgram membrane sample. In contrast, our centrifugal proteomic reactor identified 25 and 19.8 transmembrane proteins per g of plasma and microsomal membrane samples, respectively. Moreover, our centrifugal proteomic reactor identified 50 -60% authentic membrane proteins from the samples, which is far greater than the 20 -30% identification reported previously using combined SDS-PAGE, 2-D LC, and 3-D LC methods for mouse liver microsomes (22). The low recovery of membrane proteins with the in-gel digestion method is most likely attributable to (1) inefficient delipidation or solubilization of proteins during gel electrophoresis, (2) inadequate resolution of proteins with high MW and/or hydrophobicity by the SDS-PAGE, and (3) sample loss as a result of incomplete transfer and extraction of proteins from the polyacrylamide gel. All of these shortcomings associated with in-gel digestion were circumvented by the proteomic reactor method. Moreover, this approach is applicable to other samples, for example we are currently Megalin Heat shock 70 kDa protein 1A ϫ ϫ ϫ ϫ ϫ ϫ using this reactor for total cell and tissue lysate and secreted protein analysis (unpublished results). Improved Identification of Microsomal Membrane Proteins-The ER and Golgi microsomes are the major subcellular organelle for the biosynthesis of various lipids, including glycerolipids, TAG, cholesterol, and sphingolipids. Regulation of the biosynthesis of these lipids has a profound impact on hepatic lipid homeostasis; one of the homeostatic aspects of hepatic lipid metabolism is VLDL assembly and secretion (48). A unique feature associated with VLDL assembly process is that although the structural protein apoB-100 contains no transmembrane segments the protein behaves like a membrane protein, thus tightly binds to membranes during the VLDL assembly process (23). For this reason, apoB-100 has been dubbed as a "secretory membrane protein." The centrifugal proteomic reactor method developed in the current study has identified multiple enzymes that are involved in glycerolipid biosynthesis (mainly acyltransferases) as well as cholesterol and sphingolipid biosynthesis. Some of these lipid synthesis enzymes are known to play an important role in VLDL assembly and secretion. The centrifugal proteomic reactor method has also identified several protein factors that play key roles in VLDL assembly and secretion, including MTP, LDL receptor, and apoE in addition to apoB-100. None of these proteins were detected by the conventional in-gel digestion method. Altogether, studies with proteins associated with the McA-RH7777 microsomal membranes provide strong evidence for the analytical power of the centrifugal proteomic reactor.
Several previously published reports have described the analysis of plasma membrane (47,49,50) and microsomal membrane proteins (49,51,52) of mouse or rat liver origin. Two observations are noteworthy when the current data are compared with those reported previously. First, the number (257) and percentage (56%) of transmembrane proteins identified in the plasma membrane fraction using the current reactor method are much greater than previously reported (supplemental Fig. S4A). Close inspection of our dataset in comparison with the reported datasets revealed marked improvement in identifying proteins involved in lipid and lipoprotein metabolism, such as the extremely large and hydrophobic apolipoprotein B-100 (Apob), lysocardiolipin acyltransferase isoform 1 (Lycat), lysophosphatidylglycerol acyltransferase 1(LOC683760), 1-acylglycerol-3-phosphate O-acyltransferase 1, 2, and (Agpat1, Agpat2, Agpat9). Elongation of very long chain fatty acids protein 5 (Elovl5), long chain fatty acid CoA ligase 3 and 4 (Acsl3, Acsl4) and sphingolipid ⌬(4)desaturase DES1 (Degs1). These proteins were identified exclusively in our microsomal membrane data. Many membrane proteins involved in transportation and signaling transduction, for example, proteins from ATP-binding cassette transporter family (Abca1, Abcb1, Abcb1b, Abcc1, Abcc4, Abcc5 and Abcf2), proteins from solute carrier (SLC) family (Slc1a4, Slc1a5, Slc2a1, Slc3a2, Slc4a2, Slc4a4, Slc6a6, Slc6a8, Slc6a9, Slc7a1, Slc7a5, Slc7a11, Slc9a1, Slc9a3r1, Slc12a7, Slc16a10, Slc20a1, Slc23a1, Slc25a24, Slc27a4, Slc29a2, Slc30a7, Slc35e1, Slc37a2, Slc38a2, Slc38a10, Slc39a1, Slc39a7, and Slc39a10) and proteins from G protein-coupled receptor family (Gprc5c, Gpr39, and Gpr56) were identified only in our plasma membrane data (see supplemental Fig. S3, in which "unique" means proteins not overlapping between different datasets). Second, the percentage of microsomal membrane proteins with TMs Ն 1 identified by the current reactor method was also much greater than the published value (supplemental Fig. S4B), with one exception of rat microsomal membrane proteins (52). In this report ("supplemental  Table in (52)). The lack of complete information of all proteins with TMs in this report (52) precludes an adequate comparison of analytical efficacy between the two studies. We compared our 955 proteins from the microsomal membrane (from one single microsomal membrane reactor experiment) to the 1269 total proteins by Mathias et al. (12) (which were identified by a combination of four distinct triton X-114 phase separation fractions: microsome fraction ϽMFϾ, pellet fraction ϽPFϾ, detergent phase ϽDPϾ, and aqueous phase ϽAPϾ), using PROMT. As shown in supplemental Fig. S5, 538 proteins overlapped between the two datasets, and the proteins predicted with TMs were about 40% in the total proteins.
The grand average of hydropathicity index (GRAVY) and number of transmembrane domains (TMs) are the two major parameters for assessing protein hydrophobicity. The GRAVY indicates the hydrophobicity of the proteins, calculated by adding the hydropathy value for each residue and dividing by the length of the sequence: positive GRAVY (hydrophobic), negative GRAVY (hydrophilic). TMs are the number of transmembrane domains predicted by the TMHMM software. We calculated the correlation coefficients of GRAVY and TMs for our data and others. The correlation coefficients between GRAVY and TMs of plasma membrane from our data, Cao et al. (47), MPIR (49)  In summary, the present centrifugation-based proteomic reactor provides an improved method in identifying membrane proteins with high degree of hydrophobicity and number of transmembrane domains. The availability of this novel technology will facilitate qualitative and quantitative analysis of hydrophobic and membrane proteins involved in lipid and lipoprotein metabolism.