Skip to main content
Biophysical Journal logoLink to Biophysical Journal
. 1982 Mar;37(3):617–624.

Quantitative characterization of the lateral distribution of membrane proteins within the lipid bilayer.

E Freire, B Snyder
PMCID: PMC1328846  PMID: 7074188

Abstract

The dependence of the lateral distribution of membrane proteins on the size, protein/lipoid molar ratio, and the magnitude of the interaction potentials has been investigated by computer modeling protein-lipid distributions with Monte Carlo calculations. These results have allowed us to develop a quantitative characterization of the distribution of membrane proteins and to correlate these distributions with experimental observables. The topological arrangement of protein domains, protein plus annular lipid domains, and free lipid domains is described in terms of radial distribution, pair connectedness, and cluster distribution functions. The radial distribution functions are used to measure the distribution of intermolecular distances between protein molecules, whereas the pair connectedness functions are used to estimate the physical extension of compositional domains. It is shown that, at characteristic protein/lipid molar ratios, previously isolated domains become connected, forming domain networks that extend over the entire membrane surface. These changes in the lateral connectivity of compositional domains are paralleled by changes in the calculated lateral diffusion coefficients and might have important implications for the regulation of diffusion controlled processes within the membrane.

Full text

PDF
624

Selected References

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

  1. Chapman D., Cornell B. A., Ellasz A. W., Perry A. Interactions of helical polypepetide segments which span the hydrocarbon region of lipid bilayers. Studies of the gramicidin A lipid-water system. J Mol Biol. 1977 Jul 5;113(3):517–538. doi: 10.1016/0022-2836(77)90236-4. [DOI] [PubMed] [Google Scholar]
  2. Correa-Freire M. C., Freire E., Barenholz Y., Biltonen R. L., Thompson T. E. Thermotropic behavior of monoglucocerebroside--dipalmitoylphosphatidylcholine multilamellar liposomes. Biochemistry. 1979 Feb 6;18(3):442–445. doi: 10.1021/bi00570a008. [DOI] [PubMed] [Google Scholar]
  3. Freire E., Snyder B. Estimation of the lateral distribution of molecules in two-component lipid bilayers. Biochemistry. 1980 Jan 8;19(1):88–94. doi: 10.1021/bi00542a014. [DOI] [PubMed] [Google Scholar]
  4. Freire E., Snyder B. Monte Carlo studies of the lateral organization of molecules in two-component lipid bilayers. Biochim Biophys Acta. 1980 Aug 14;600(3):643–654. doi: 10.1016/0005-2736(80)90468-x. [DOI] [PubMed] [Google Scholar]
  5. Gomez-Fernandez J. C., Goni F. M., Bach D., Restall C. J., Chapman D. Protein-lipid interaction. Biophysical studies of (Ca2+ + Mg2+)-ATPase reconstituted systems. Biochim Biophys Acta. 1980 Jun 6;598(3):502–516. doi: 10.1016/0005-2736(80)90031-0. [DOI] [PubMed] [Google Scholar]
  6. Hui S. W., Parsons D. F. Direct observation of domains in wet lipid bilayers. Science. 1975 Oct 24;190(4212):383–384. doi: 10.1126/science.1179216. [DOI] [PubMed] [Google Scholar]
  7. Jost P. C., Griffith O. H., Capaldi R. A., Vanderkooi G. Evidence for boundary lipid in membranes. Proc Natl Acad Sci U S A. 1973 Feb;70(2):480–484. doi: 10.1073/pnas.70.2.480. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Kang S. Y., Gutowsky H. S., Hsung J. C., Jacobs R., King T. E., Rice D., Oldfield E. Nuclear magnetic resonance investigation of the cytochrome oxidase--phospholipid interaction: a new model for boundary lipid. Biochemistry. 1979 Jul 24;18(15):3257–3267. doi: 10.1021/bi00582a010. [DOI] [PubMed] [Google Scholar]
  9. Lindblom G., Johansson L. B., Arvidson G. Effect of cholesterol in membranes. Pulsed nuclear magnetic resonance measurements of lipid lateral diffusion. Biochemistry. 1981 Apr 14;20(8):2204–2207. doi: 10.1021/bi00511a020. [DOI] [PubMed] [Google Scholar]
  10. Marsh D., Watts A., Maschke W., Knowles P. F. Protein--immobilized lipid in dimyristoylphosphatidylcholine-substituted cytochrome oxidase: evidence for both boundary and trapped-bilayer lipid. Biochem Biophys Res Commun. 1978 Mar 30;81(2):397–402. doi: 10.1016/0006-291x(78)91546-2. [DOI] [PubMed] [Google Scholar]
  11. Owicki J. C., McConnell H. M. Lateral diffusion in inhomogeneous membranes. Model membranes containing cholesterol. Biophys J. 1980 Jun;30(3):383–397. doi: 10.1016/S0006-3495(80)85103-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Paddy M. R., Dahlquist F. W., Davis J. H., Bloom M. Dynamical and temperature-dependent effects of lipid-protein interactions. Application of deuterium nuclear magnetic resonance and electron paramagnetic resonance spectroscopy to the same reconstitutions of cytochrome c oxidase. Biochemistry. 1981 May 26;20(11):3152–3162. doi: 10.1021/bi00514a026. [DOI] [PubMed] [Google Scholar]
  13. Papahadjopoulos D., Vail W. J., Pangborn W. A., Poste G. Studies on membrane fusion. II. Induction of fusion in pure phospholipid membranes by calcium ions and other divalent metals. Biochim Biophys Acta. 1976 Oct 5;448(2):265–283. doi: 10.1016/0005-2736(76)90241-8. [DOI] [PubMed] [Google Scholar]
  14. Pearson R. P., Hui S. W., Stewart T. P. Correlative statistical analysis and computer modelling of intramembraneous particle distributions in human erythrocyte membranes. Biochim Biophys Acta. 1979 Nov 2;557(2):265–282. doi: 10.1016/0005-2736(79)90326-2. [DOI] [PubMed] [Google Scholar]
  15. Rice D., Oldfield E. Deuterium nuclear magnetic resonance studies of the interaction between dimyristoylphosphatidylcholine and gramicidin A'. Biochemistry. 1979 Jul 24;18(15):3272–3279. doi: 10.1021/bi00582a012. [DOI] [PubMed] [Google Scholar]
  16. Satir B. Genetic control of membrane mosaicism. J Supramol Struct. 1976;5(3):381–389. doi: 10.1002/jss.400050310. [DOI] [PubMed] [Google Scholar]
  17. Shimshick E. J., McConnell H. M. Lateral phase separation in phospholipid membranes. Biochemistry. 1973 Jun 5;12(12):2351–2360. doi: 10.1021/bi00736a026. [DOI] [PubMed] [Google Scholar]
  18. Snyder B., Freire E. Compositional domain structure in phosphatidylcholine--cholesterol and sphingomyelin--cholesterol bilayers. Proc Natl Acad Sci U S A. 1980 Jul;77(7):4055–4059. doi: 10.1073/pnas.77.7.4055. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Wallace B. A., Engelman D. M. The planar distributions of surface proteins and intramembrane particles in Acholeplasma laidlawii are differentially affected by the physical state of membrane lipids. Biochim Biophys Acta. 1978 Apr 20;508(3):431–449. doi: 10.1016/0005-2736(78)90090-1. [DOI] [PubMed] [Google Scholar]
  20. van Dijck P. W., de Kruijff B., Verkleij A. J., van Deenen L. L., de Gier J. Comparative studies on the effects of pH and Ca2+ on bilayers of various negatively charged phospholipids and their mixtures with phosphatidylcholine. Biochim Biophys Acta. 1978 Sep 11;512(1):84–96. doi: 10.1016/0005-2736(78)90219-5. [DOI] [PubMed] [Google Scholar]

Articles from Biophysical Journal are provided here courtesy of The Biophysical Society

RESOURCES