Wiegel F W, DeLisi C
Am J Physiol. 1982 Nov;243(5):R475-9. doi: 10.1152/ajpregu.1982.243.5.R475.
The paths followed by ligands as they react with or dissociate from cell surface receptors may include weak association with nonreceptor portions of the surface followed by lateral diffusion in the plane of the membrane to a receptor. The change in dimensionality of the diffusion process by utilization of these nonspecific paths has been invoked by a number of investigators as a mechanism for enhancing reaction rate in biological systems. This paper extends our previous work on the calculation of diffusive rate constants for ligand-receptor paths. We find that they have little effect on rate constants unless the number of free receptors per cell has been reduced to less than or equal to 10(2). This number represents better than 90% occupancy for most eukaryotes, suggesting that the dimensional change mechanism is of limited consequence. We show further that when the free receptor number is low enough for rate enhancement, then the primary parameter of consequence is D'K*/D, where D' and D are the two- and three-dimensional diffusion coefficients, respectively, and K* the nonspecific affinity. A 10-fold rate enhancement with 100 free receptors requires that this parameter be of order 10(-3). This value is barely within the lower limit imposed by currently available experimental information, casting doubt on the relevance of nonspecific paths in cellular systems.
配体与细胞表面受体反应或从其解离时所遵循的路径可能包括与表面非受体部分的弱结合,随后在膜平面内横向扩散至受体。许多研究人员提出,利用这些非特异性路径改变扩散过程的维度是提高生物系统反应速率的一种机制。本文扩展了我们之前关于配体 - 受体路径扩散速率常数计算的工作。我们发现,除非每个细胞的游离受体数量减少到小于或等于10²,否则它们对速率常数影响很小。对于大多数真核生物而言,这个数量代表着超过90%的占有率,这表明维度变化机制的作用有限。我们进一步表明,当游离受体数量低到足以提高反应速率时,起主要作用的参数是D'K*/D,其中D'和D分别是二维和三维扩散系数,K*是非特异性亲和力。对于100个游离受体,速率提高10倍要求该参数约为10⁻³。这个值刚好处于现有实验信息所施加的下限范围内,这使得人们对细胞系统中非特异性路径的相关性产生怀疑。