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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5
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pubmed:dateCreated |
1989-7-7
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pubmed:abstractText |
A two-dimensional version of the generalized Smoluchowski equation is used to analyze the time (or distance) dependent self diffusion of interacting membrane proteins in concentrated membrane systems. This equation provides a well established starting point for descriptions of the diffusion of particles that interact through both direct and hydrodynamic forces; in this initial work only the effects of direct interactions are explicitly considered. Data describing diffusion in the presence of hard-core repulsions, soft repulsions, and soft repulsions with weak attractions are presented. The effect that interactions have on the self-diffusion coefficient of a real protein molecule from mouse liver gap junctions is also calculated. The results indicate that self diffusion is always inhibited by direct interactions; this observation is interpreted in terms of the caging that will exist at finite protein concentration. It is also noted that, over small distance scales, the diffusion coefficient is determined entirely by the very strong Brownian forces; therefore, as a function of displacement the self-diffusion coefficient decays (rapidly) from its value at infinite dilution to its steady-state interaction-averaged value. The steady-state self-diffusion coefficient describes motion over distance scales that range from approximately 10 nm to cellular dimensions and is the quantity measured in fluorescence recovery after photobleaching experiments. The short-ranged behavior of the diffusion coefficient is important on the interparticle-distance scale and may therefore influence the rate at which nearest-neighbor collisional processes take place. The hard-disk theoretical results presented here are in excellent agreement with lattice Monte-Carlo results obtained by other workers. The concentration dependence of experimentally measured diffusion coefficients of antibody-hapten complexes bound to the membrane surface is consistent with that predicted by the theory. The variation in experimental diffusion coefficients of integral membrane proteins is greater than that predicted by the theory, and may also reflect protein-induced perturbations in membrane viscosity.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/2720077-1059096,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2720077-17834156,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2720077-19431688,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2720077-291959,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2720077-3006037,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2720077-3207834,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2720077-3276003,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/2720077-3651562,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2720077-3778578,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/2720077-7295677
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0006-3495
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
55
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
817-33
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pubmed:dateRevised |
2010-9-9
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pubmed:meshHeading |
pubmed-meshheading:2720077-Animals,
pubmed-meshheading:2720077-Diffusion,
pubmed-meshheading:2720077-Intercellular Junctions,
pubmed-meshheading:2720077-Kinetics,
pubmed-meshheading:2720077-Liver,
pubmed-meshheading:2720077-Mathematics,
pubmed-meshheading:2720077-Membrane Potentials,
pubmed-meshheading:2720077-Membrane Proteins,
pubmed-meshheading:2720077-Mice,
pubmed-meshheading:2720077-Models, Theoretical
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pubmed:year |
1989
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pubmed:articleTitle |
Self diffusion of interacting membrane proteins.
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pubmed:affiliation |
Cell and Molecular Biology Division, Lawrence Berkeley Laboratory, California 94720.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.
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