McKinley D N
J Theor Biol. 1983 Aug 7;103(3):405-19. doi: 10.1016/0022-5193(83)90294-1.
Transport of receptors by the coated vesicle pathway entails assembly of clathrin triskelions into a lattice in conjunction with receptors in a membrane. The processes by which the receptors are concentrated, the lattice is assembled, transformed into a cage during vesiculation, and subsequently removed from pinched off vesicles are not understood in regard to mechanism, energetics or control. Tubulin and actin assembly are looked to for analogies applicable to clathrin. The present model supposes that clathrin assembly is energy linked and can be described by kinetic equations of the same general form as those for treadmilling in linear polymers. The coat lattice assembles in a steady state involving the degradation of a high energy form of the clathrin triskelions. Diffuse endocytosis receptors are assumed to be associated with individual triskelions and to be able to trigger clustering and coated pit formation by influencing the assembly kinetics of the bound triskelions. A generalization of the treadmilling scheme is proposed by which the kinetic parameters associated with clathrin polymerization can shift simultaneously for an entire lattice to favor alternatively net assembly or disassembly. This shift is effected by a coordinated conversion of the lattice bound receptors. The conversion of the receptors in turn depends on some global property of the membrane compartments (arguably pH, calcium concentration or transmembrane voltage) which is likely to change as a consequence of vesiculation. Thereby, lattice disassembly can be coordinated with the topological conversion from coated pit to coated vesicle.
通过被膜小泡途径运输受体需要网格蛋白三脚蛋白复合体与膜中的受体一起组装成晶格。关于受体如何浓缩、晶格如何组装、在形成小泡过程中如何转变为笼子以及随后如何从缢断的小泡中去除等过程,在机制、能量学或调控方面尚不清楚。人们期望微管蛋白和肌动蛋白组装能为适用于网格蛋白的情况提供类比。当前模型假定网格蛋白组装与能量相关联,并且可以用与线性聚合物中踏车行为相同一般形式的动力学方程来描述。被膜晶格以一种稳态组装,涉及网格蛋白三脚蛋白复合体高能形式的降解。假定扩散性内吞受体与单个三脚蛋白复合体相关联,并能够通过影响结合的三脚蛋白复合体的组装动力学来触发聚集和被膜小窝形成。提出了一种踏车行为模式的推广,据此与网格蛋白聚合相关的动力学参数可以同时为整个晶格发生变化,以交替地有利于净组装或拆卸。这种变化是由被膜晶格结合受体的协同转变实现的。受体的转变反过来又取决于膜隔室的某些全局性质(可以说是pH值、钙浓度或跨膜电压),而这些性质很可能会因小泡形成而发生变化。由此,晶格拆卸可以与从被膜小窝到被膜小泡的拓扑转变相协调。