Linderman J J, Lauffenburger D A
Department of Chemical Engineering, University of Michigan, Ann Arbor 48109.
J Theor Biol. 1988 May 21;132(2):203-45. doi: 10.1016/s0022-5193(88)80157-7.
After binding to specific cell surface receptors, many extracellular ligand molecules are internalized via the process termed receptor-mediated endocytosis. Within the cell, in endosomes, a sorting process occurs: receptors and ligands are directed along various intracellular pathways. The extent of this intracellular separation of receptors from ligands has been shown experimentally to vary with receptor and ligand properties such as binding affinity and valency. In this paper, we propose and analyze a simple model mechanism for the sorting process based on binding and dissociation kinetics along with diffusive molecular transport. We show that the outcome of the sorting process can be directly linked to measurable parameters such as the intrinsic rate constants for the binding to, dissociation from, and crosslinking of receptors by ligands. We further show that this mechanism is able to account for the wide range of reported experimental observations. Manipulation of ligand and receptor properties guided by the results presented here may enable the outcome of the sorting process to be controlled.
许多细胞外配体分子在与特定细胞表面受体结合后,会通过称为受体介导的内吞作用的过程被内化。在细胞内的内体中,会发生一种分选过程:受体和配体沿着各种细胞内途径被引导。实验表明,受体与配体在细胞内这种分离的程度会因受体和配体的性质(如结合亲和力和价态)而有所不同。在本文中,我们基于结合和解离动力学以及扩散性分子转运,提出并分析了一种用于分选过程的简单模型机制。我们表明,分选过程的结果可以直接与可测量的参数相关联,例如配体与受体结合、解离以及交联的固有速率常数。我们进一步表明,这种机制能够解释大量已报道的实验观察结果。根据此处给出的结果对配体和受体性质进行操控,可能会使分选过程的结果得到控制。