Skip to main content
Log in

Topography and functional information of plasma membrane

  • Published:
Science in China Series C: Life Sciences Aims and scope Submit manuscript

Abstract

By using atomic force microscope (AFM), the topography and function of the plasmalemma surface of the isolated protoplasts from winter wheat mesophyll cells were observed, and compared with dead protoplasts induced by dehydrating stress. The observational results revealed that the plasma membrane of living protoplasts was in a state of polarization. Lipid layers of different cells and membrane areas exhibited distinct active states. The surfaces of plasma membranes were unequal, and were characterized of regionalisation. In addition, lattice structures were visualized in some regions of the membrane surface. These typical structures were assumed to be lipid molecular complexes, which were measured to be 15.8±0.09 nm in diameter and 1.9±0.3 nm in height. Both two-dimensional and three-dimensional imaging showed that the plasmalemma surfaces of winter wheat protoplasts were covered with numerous protruding particles. In order to determine the chemical nature of the protruding particles, living protoplasts were treated by proteolytic enzyme. Under the effect of enzyme, large particles became relatively looser, resulting that their width was increased and their height decreased. The results demonstrated that these particles were likely to be of protein nature. These protein particles at plasmalemma surface were different in size and unequal in distribution. The diameter of large protein particles ranged from 200 to 440 nm, with a central micropore, and the apparent height of them was found to vary from 12 to 40 nm. The diameter of mid-sized protein particles was between 40–60 nm, and a range of 1.8–5 nm was given for the apparent height of them. As for small protein particles, obtained values were 12–40 nm for their diameter and 0.7–2.2 nm for height. Some invaginated pits were also observed at the plasma membrane. They were formed by the endocytosis of protoplast. Distribution density of them at plasmalemma was about 16 pits per 15 μm2. According to their size, we classified the invaginated pits into two types-larger pits measuring 139 nm in diameter and 7.2 nm in depth, and smaller pits measuring 96 nm in diameter and 2.3 nm in depth. On dehydration-induced dead protoplasts, the degree of polarization of plasma membranes decreased. Lipid molecular layers appeared relatively smooth, and the quantity of integral proteins reduced a lot. Invaginated pits were still detectable at the membrane surface, but due to dehydration-induced protoplast contraction, the orifice diameter of pits reduced, and their depth increased. Larger pits averagely measuring 47.4 nm in diameter and 31.9 nm in depth, and smaller pits measuring 26.5 nm in diameter and 43 nm in depth at average. The measured thickness of plasma membranes of mesophyll cells from winter wheat examined by AFM was 6.6–9.8 nm, thicker in regions covered with proteins.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Lin K C. Advances in single biomolecule research. Acta Biophys Sin (in Chinese), 2001, 17(3): 411–418

    CAS  Google Scholar 

  2. Yuan C B, Ding D S, Lu Z H, et. al. Atomic force microscopic investigation on the DMPC Langmuir-Blodgett films. Acta Biophys Sin (in Chinese), 1996, 12(1): 67–70

    Google Scholar 

  3. Wang L, Song Y H, Han X J, et. al. Growth of cationic lipid toward bilayer lipid membrane by solution spreading: Scanning probe microscopy study. Chem Phys Lipids, 2003, 123: 177–185

    Article  PubMed  CAS  Google Scholar 

  4. Jian L C, Sun L H, Sun D L. Change in ATPase activity at plasmallemma and tonoplast during cold hardening of wheat seeding. Acta Biol Exp Sin (in Chinese), 1983, 16: 133–138

    Google Scholar 

  5. Wang H, Sun D L, Lu C F, et al. Stability effects of cold-acclimation on the plasmolemma Ca2+-ATPase of winter wheat seedlings. Acta Botan Sin (in Chinese), 1998, 40(12): 1098–1101

    CAS  Google Scholar 

  6. Sun D L, Wang H, Jian L C. The stabilization on the plasmalemma calciumpump (Ca2+-ATPase) in winter wheat seedlings by the coldresistant agent CR-4. Chin Bull Botany (in Chinese), 1998, 15(2): 50–54

    Google Scholar 

  7. Wang K R. Cytobiology. Beijing: Beijing Normal University Press, 1998. 52–110

    Google Scholar 

  8. Bourdieu L, Ronsin O, Chatenay D. Molecular positional order in Langmuir-Blodgett films by atomic force microscopy. Science, 1993, 259: 798–801

    Article  PubMed  CAS  Google Scholar 

  9. Meyer E, Howald L, Overney R M, et al. Molecular-resolution images of Langmuir-Blodgett films using atomic force microscopy. Nature, 1991, 349: 398–400

    Article  CAS  Google Scholar 

  10. Tokumasu F, Jin A J, Feigenson G W, et al. Atomic force microscopy of nanometric liposome adsorption and nanoscopic membrane domain formation. Ultramicroscopy, 2003, 97: 217–227

    Article  PubMed  CAS  Google Scholar 

  11. Karrasch S, Hegerl R, Hoh J H, et al. Atomic force microscopy produces faithful high-resolution images of protein surfaces in an aqueous environment. Proc Natl Acad Sci USA, 1994, 91: 836–838

    Article  PubMed  CAS  Google Scholar 

  12. Genevieve Devaud, Paul S, Furcinitti, et al. Direct observation of defect structure in protein crystals by atomic force and transmission electron microscopy. Biophys J, 1992, 63: 630–638

    Article  Google Scholar 

  13. Lacapere J-J, Stokes D L, Chatenay D. Atomic force microscopy of three-dimensional membrane protein crystals: Ca-ATPase of sarcoplasmic reticulum. Biophys J, 1992, 63: 303–308.

    PubMed  CAS  Google Scholar 

  14. Kolomytkin O V, Golubok A O, Davydov D N, et al. Ionic channels in Langmuir-Blodgett films imaged by a scanning tunneling microscope. Biophys J, 1991, 59: 889–893

    PubMed  CAS  Google Scholar 

  15. Vogel J, Bendas G, Bakowsky U, et al. The role of glycolipids in mediating cell adhesion: A flow chamber study. Biochim Biophys Acta, 1998, 1372: 205–215

    Article  PubMed  CAS  Google Scholar 

  16. Oesterhelt F, Oesterhelt D, Pfeiffer M, et al. Unfolding Pathways of individual bacteriorhodopsins. Science, 2000, 288: 143–146

    Article  PubMed  CAS  Google Scholar 

  17. You H X, Lau J M, Zhang S W, et al. Atomic force microscopy imaging of living cells: A prelimimary study of the disruptive effect of the cantilever tip on cell morphology. Ultramicroscopy, 2000, 82: 297–305

    Article  PubMed  CAS  Google Scholar 

  18. Dufrene Y F. Application of atomic force microscopy to microbial surfaces: From reconstituted cell surface layers to living cells. Micron, 2001, 32: 153–165

    Article  PubMed  CAS  Google Scholar 

  19. Ehrenhofer U, Rakowska A, Schneider S W, et al. The atomic force microscopy detects ATP-sensitive protein clusters in the plasma membrane of transformed MIDCK cells. Cell Biol Int, 1997, 21(11): 737–746

    Article  PubMed  CAS  Google Scholar 

  20. Crevecoeur M, Lesniewska E, Vie V, et al. Atomic-force microscopy imaging of plasma membrane purified from spinach leaves. Protoplasma, 2000, 212: 46–55

    Article  Google Scholar 

  21. Kaftan D, Brumfeld V, Nevo R, et al. From chloroplasts to photosystems: in situ scanning force microscopy on intact thylakoid membrane. EMBO J, 2002, 21(22): 6146–6153

    Article  PubMed  CAS  Google Scholar 

  22. Jena B P. Fusion Pore or porosome: Structure and dynamics. J Endocrinol, 2003, 176: 169–174

    Article  PubMed  CAS  Google Scholar 

  23. Jena B P, Cho S J, Jeremic A, et al. Structure and composition of the fusion pore. Biophysical J, 2003, 84: 1337–1343

    CAS  Google Scholar 

  24. Janovjak H, Kedrov A, David A, et al. Imaging and detecting molecular interaction of single transmembrane proteins. Neurobiol Aging, 2006, 27: 546–561

    Article  PubMed  CAS  Google Scholar 

  25. Daniel J, Müller K, Sapra T, et al. Single-molecular studies of membrane proteins. Curr Opin Structu Biol, 2006, 16: 489–495

    Article  CAS  Google Scholar 

  26. Li G Y, Xi N, Wang D H. Probing membrane proteins using atomic force microscopy. J Biochem, 2006, 97: 1191–1197

    CAS  Google Scholar 

  27. Müller D J, Janovjk H, Lehto T, et al. Observing structure, function and assembly of single proteins by AFM. Prog Biophys Mol Biol, 2002, 79: 1–43

    Article  PubMed  Google Scholar 

  28. Betz T, Bakowsky U, Müller M R, et al. Conformational change membrane proteins leads to shape change of red blood cells. Bioelectrochemistry, 2007, 1: 122–126

    Article  CAS  Google Scholar 

  29. Domenech O, Merino-Montero S, Montero M T, et al. Surface planar bilayers of phospholipids used in protein membrane reconstitution: An atomic force microscopy study. Coll Surf B-Biointerfaces. 2006, 47: 102–106

    Article  CAS  Google Scholar 

  30. Chen J M, Sun D L. Biological membranes and membrane proteins: From single molecules to cells. Chin Bull Botany (in Chinese), 2003, 20(6): 763–765

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Sun DeLan.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sun, D., Chen, J., Song, Y. et al. Topography and functional information of plasma membrane. Sci. China Ser. C-Life Sci. 51, 95–103 (2008). https://doi.org/10.1007/s11427-008-0007-y

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11427-008-0007-y

Keywords

Navigation