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细胞表面的分子流动性。

Molecular mobility on the cell surface.

作者信息

Webb W W, Barak L S, Tank D W, Wu E S

出版信息

Biochem Soc Symp. 1981(46):191-205.

PMID:7039623
Abstract

Many measurements of lateral diffusion of proteins and lipids on cell membranes and lipid model membranes have become available through application of fluorescence photobleaching recovery methods. A puzzling aspect of these results is slow diffusion and partial immobilization of protein molecules on the cell surface. Observed protein diffusion coefficients on vertebrate structural tissue cells are consistently D less than or equal to 10(-10) cm2/s, while lipid analogues diffuse with D approx. 10(-8) cm2/s. Substantial fractions of the cell membrane proteins are not diffusible. In a pure viscous membrane, theoretical fluid dynamics has suggested only small differences between lipid and protein diffusion coefficients. Measurements of protein diffusion in model membranes recently showed D less than or equal to 10(-9) cm2/s, as expected. Recent experiments on cell membranes show that uncoupling of the membrane from the cytoskeleton by formation of blebs releases the membrane protein molecules so that diffusion is enhanced to D greater than or equal to 10(-9) cm2/s and the non-diffusible fraction is eliminated.

摘要

通过应用荧光光漂白恢复方法,已经获得了许多关于蛋白质和脂质在细胞膜及脂质模型膜上横向扩散的测量结果。这些结果中一个令人困惑的方面是蛋白质分子在细胞表面的扩散缓慢且部分固定。在脊椎动物结构组织细胞上观察到的蛋白质扩散系数始终为D≤10^(-10) cm²/s,而脂质类似物的扩散系数约为D≈10^(-8) cm²/s。相当一部分细胞膜蛋白是不可扩散的。在纯粘性膜中,理论流体动力学表明脂质和蛋白质扩散系数之间只有微小差异。最近在模型膜中进行的蛋白质扩散测量显示,正如预期的那样,D≤10^(-9) cm²/s。最近对细胞膜的实验表明,通过形成泡将膜与细胞骨架解偶联会释放膜蛋白分子,从而使扩散增强到D≥10^(-9) cm²/s,并且不可扩散部分被消除。

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