Department of Biomedical Engineering, The University of Texas at Austin, Austin, TX 78712, USA.
Department of Biomedical Engineering, The University of Texas at Austin, Austin, TX 78712, USA; Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, TX 78712, USA.
J Mol Biol. 2018 Aug 3;430(16):2293-2308. doi: 10.1016/j.jmb.2018.03.024. Epub 2018 Apr 5.
Cellular membranes must undergo remodeling to facilitate critical functions including membrane trafficking, organelle biogenesis, and cell division. An essential step in membrane remodeling is membrane fission, in which an initially continuous membrane surface is divided into multiple, separate compartments. The established view has been that membrane fission requires proteins with conserved structural features such as helical scaffolds, hydrophobic insertions, and polymerized assemblies. In this review, we discuss these structure-based fission mechanisms and highlight recent findings from several groups that support an alternative, structure-independent mechanism of membrane fission. This mechanism relies on lateral collisions among crowded, membrane-bound proteins to generate sufficient steric pressure to drive membrane vesiculation. As a stochastic process, this mechanism contrasts with the paradigm that deterministic protein structures are required to drive fission, raising the prospect that many more proteins may participate in fission than previously thought. Paradoxically, our recent work suggests that intrinsically disordered domains may be among the most potent drivers of membrane fission, owing to their large hydrodynamic radii and substantial chain entropy. This stochastic view of fission also suggests new roles for the structure-based fission proteins. Specifically, we hypothesize that in addition to driving fission directly, the canonical fission machines may facilitate the enrichment and organization of bulky disordered protein domains in order to promote membrane fission by locally amplifying protein crowding.
细胞膜必须进行重塑,以促进包括膜运输、细胞器发生和细胞分裂在内的关键功能。膜重塑的一个基本步骤是膜裂变,其中初始连续的膜表面被分成多个独立的隔室。已确立的观点是,膜裂变需要具有保守结构特征的蛋白质,如螺旋支架、疏水性插入物和聚合组装体。在这篇综述中,我们讨论了这些基于结构的裂变机制,并强调了来自几个小组的最近发现,这些发现支持了一种替代的、不依赖结构的膜裂变机制。该机制依赖于拥挤的、膜结合蛋白之间的侧向碰撞,以产生足够的位阻压力来驱动膜泡形成。作为一个随机过程,这种机制与需要确定的蛋白质结构来驱动裂变的范式形成对比,这提出了许多更多的蛋白质可能参与裂变的可能性,比以前想象的要多。矛盾的是,我们最近的工作表明,固有无序域可能是最有效的膜裂变驱动因子之一,这要归功于它们较大的流体力学半径和大量的链熵。这种裂变的随机观点也为基于结构的裂变蛋白提出了新的作用。具体来说,我们假设,除了直接驱动裂变之外,经典的裂变机器还可以促进大体积无序蛋白质域的富集和组织,以便通过局部放大蛋白质拥挤来促进膜裂变。