Pucadyil Thomas J, Schmid Sandra L
Department of Cell Biology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Cell. 2008 Dec 26;135(7):1263-75. doi: 10.1016/j.cell.2008.11.020. Epub 2008 Dec 11.
The GTPase dynamin assembles at the necks of budded vesicles in vivo and functions in membrane fission. We have developed fluid supported bilayers with excess membrane reservoir, (SUPER) templates, to assay vesicle formation and membrane fission. Consistent with previous studies, in the absence of GTP, dynamin assembles in spirals, forming long membrane tubules. GTP addition triggers disassembly, but not membrane fission, arguing against models in which fission is mediated by concerted and global GTP-driven conformational changes. In contrast, under physiological conditions in the constant presence of GTP, dynamin mediates membrane fission. Under these conditions, fluorescently labeled dynamin cooperatively organizes into self-limited assemblies that continuously cycle at the membrane and drive vesicle release. When visualized at the necks of emergent vesicles, self-limited dynamin assemblies display intensity fluctuations and persist for variable time periods before fission. Thus, self-limited assemblies of dynamin generated in the constant presence of GTP catalyze membrane fission.
GTP酶发动蛋白在体内芽生小泡的颈部组装,并在膜裂变中发挥作用。我们开发了具有过量膜储备的流体支撑双层膜(SUPER)模板,以检测小泡形成和膜裂变。与之前的研究一致,在没有GTP的情况下,发动蛋白呈螺旋状组装,形成长的膜小管。添加GTP会触发解体,但不会引发膜裂变,这与裂变由协同的全局GTP驱动的构象变化介导的模型相悖。相反,在生理条件下,持续存在GTP时,发动蛋白介导膜裂变。在这些条件下,荧光标记的发动蛋白协同组织成自我限制的组装体,这些组装体在膜上持续循环并驱动小泡释放。当在新生小泡的颈部观察时,自我限制的发动蛋白组装体显示出强度波动,并在裂变前持续不同的时间段。因此,在持续存在GTP的情况下产生的发动蛋白自我限制组装体催化膜裂变。