Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1979 Oct;76(10):4750–4754. doi: 10.1073/pnas.76.10.4750

Theory of protein-lipid and protein-protein interactions in bilayer membranes.

J C Owicki, H M McConnell
PMCID: PMC413014  PMID: 291895

Abstract

A model for protein-lipid interactions in bilayer membranes where the proteins are very dilute is extended to higher protein concentration, where appreciable lipid-mediated protein-protein interactions occur. It is found that proteins may change the lipid phase transition temperature and that they weaken the phase transition. There exists a critical protein concentration above which the sharp lipid phase transition is abolished. The model also qualitatively reproduces several experimental observations on the physical behavior of bilayers formed from mixtures of cholesterol and phosphatidylcholines.

Full text

PDF
4750

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Chapman D., Gómez-Fernández J. C., Goñi F. M. Intrinsic protein--lipid interactions. Physical and biochemical evidence. FEBS Lett. 1979 Feb 15;98(2):211–223. doi: 10.1016/0014-5793(79)80186-6. [DOI] [PubMed] [Google Scholar]
  2. Curatolo W., Sakura J. D., Small D. M., Shipley G. G. Protein-lipid interactions: recombinants of the proteolipid apoprotein of myelin with dimyristoyllecithin. Biochemistry. 1977 May 31;16(11):2313–2319. doi: 10.1021/bi00630a001. [DOI] [PubMed] [Google Scholar]
  3. Curatolo W., Verma S. P., Sakura J. D., Small D. M., Shipley G. G., Wallach D. F. Structural effects of myelin proteolipid apoprotein on phospholipids: a Raman spectroscopic study. Biochemistry. 1978 May 2;17(9):1802–1807. doi: 10.1021/bi00602a035. [DOI] [PubMed] [Google Scholar]
  4. Dahlquist F. W., Muchmore D. C., Davis J. H., Bloom M. Deuterium magnetic resonance studies of the interaction of lipids with membrane proteins. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5435–5439. doi: 10.1073/pnas.74.12.5435. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Estep T. N., Mountcastle D. B., Biltonen R. L., Thompson T. E. Studies on the anomalous thermotropic behavior of aqueous dispersions of dipalmitoylphosphatidylcholine-cholesterol mixtures. Biochemistry. 1978 May 16;17(10):1984–1989. doi: 10.1021/bi00603a029. [DOI] [PubMed] [Google Scholar]
  6. Favre E., Baroin A., Bienvenue A., Devaux P. F. Spin-label studies of lipid-protein interactions in retinal rod outer segment membranes. Fluidity of the boundary layer. Biochemistry. 1979 Apr 3;18(7):1156–1162. doi: 10.1021/bi00574a006. [DOI] [PubMed] [Google Scholar]
  7. Grant C. W., McConnell H. M. Glycophorin in lipid bilayers. Proc Natl Acad Sci U S A. 1974 Dec;71(12):4653–4657. doi: 10.1073/pnas.71.12.4653. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Janiak M. J., Small D. M., Shipley G. G. Nature of the Thermal pretransition of synthetic phospholipids: dimyristolyl- and dipalmitoyllecithin. Biochemistry. 1976 Oct 19;15(21):4575–4580. doi: 10.1021/bi00666a005. [DOI] [PubMed] [Google Scholar]
  9. Kleemann W., McConnell H. M. Lateral phase separations in Escherichia coli membranes. Biochim Biophys Acta. 1974 Apr 29;345(2):220–230. doi: 10.1016/0005-2736(74)90260-0. [DOI] [PubMed] [Google Scholar]
  10. Mabrey S., Mateo P. L., Sturtevant J. M. High-sensitivity scanning calorimetric study of mixtures of cholesterol with dimyristoyl- and dipalmitoylphosphatidylcholines. Biochemistry. 1978 Jun 13;17(12):2464–2468. doi: 10.1021/bi00605a034. [DOI] [PubMed] [Google Scholar]
  11. Marsh D., Barrantes F. J. Immobilized lipid in acetylcholine receptor-rich membranes from Torpedo marmorata. Proc Natl Acad Sci U S A. 1978 Sep;75(9):4329–4333. doi: 10.1073/pnas.75.9.4329. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Oldfield E., Gilmore R., Glaser M., Gutowsky H. S., Hshung J. C., Kang S. Y., King T. E., Meadows M., Rice D. Deuterium nuclear magnetic resonance investigation of the effects of proteins and polypeptides on hydrocarbon chain order in model membrane systems. Proc Natl Acad Sci U S A. 1978 Oct;75(10):4657–4660. doi: 10.1073/pnas.75.10.4657. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Owicki J. C., Springgate M. W., McConnell H. M. Theoretical study of protein--lipid interactions in bilayer membranes. Proc Natl Acad Sci U S A. 1978 Apr;75(4):1616–1619. doi: 10.1073/pnas.75.4.1616. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Pink D. A., Chapman D. Protein-lipid interactions in bilayer membranes: a lattice model. Proc Natl Acad Sci U S A. 1979 Apr;76(4):1542–1546. doi: 10.1073/pnas.76.4.1542. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Rubenstein J. L., Smith B. A., McConnell H. M. Lateral diffusion in binary mixtures of cholesterol and phosphatidylcholines. Proc Natl Acad Sci U S A. 1979 Jan;76(1):15–18. doi: 10.1073/pnas.76.1.15. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Warren G. B., Toon P. A., Birdsall N. J., Lee A. G., Metcalfe J. C. Reversible lipid titrations of the activity of pure adenosine triphosphatase-lipid complexes. Biochemistry. 1974 Dec 31;13(27):5501–5507. doi: 10.1021/bi00724a008. [DOI] [PubMed] [Google Scholar]
  17. Wilkinson D. A., Nagle J. F. A differential dilatometer. Anal Biochem. 1978 Jan;84(1):263–271. doi: 10.1016/0003-2697(78)90509-2. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES