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发动蛋白的GTP酶循环与膜的挤压和释放相偶联,导致自发裂变。

GTPase cycle of dynamin is coupled to membrane squeeze and release, leading to spontaneous fission.

作者信息

Bashkirov Pavel V, Akimov Sergey A, Evseev Alexey I, Schmid Sandra L, Zimmerberg Joshua, Frolov Vadim A

机构信息

Program on Physical Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Bethesda, MD 20892-1855, USA.

出版信息

Cell. 2008 Dec 26;135(7):1276-86. doi: 10.1016/j.cell.2008.11.028. Epub 2008 Dec 11.

Abstract

The GTPase dynamin is critically involved in membrane fission during endocytosis. How does dynamin use the energy of GTP hydrolysis for membrane remodeling? By monitoring the ionic permeability through lipid nanotubes (NT), we found that dynamin was capable of squeezing NT to extremely small radii, depending on the NT lipid composition. However, long dynamin scaffolds did not produce fission: instead, fission followed GTPase-dependent cycles of assembly and disassembly of short dynamin scaffolds and involved a stochastic process dependent on the curvature stress imposed by dynamin. Fission happened spontaneously upon NT release from the scaffold, without leakage. Our calculations revealed that local narrowing of NT could induce cooperative lipid tilting, leading to self-merger of the inner monolayer of NT (hemifission), consistent with the absence of leakage. We propose that dynamin transmits GTP's energy to periodic assembling of a limited curvature scaffold that brings lipids to an unstable intermediate.

摘要

GTP酶发动蛋白在内吞作用期间的膜裂变过程中起着关键作用。发动蛋白如何利用GTP水解的能量进行膜重塑?通过监测脂质纳米管(NT)的离子通透性,我们发现发动蛋白能够根据NT的脂质组成将NT挤压到极小的半径。然而,长的发动蛋白支架不会产生裂变:相反,裂变伴随着短发动蛋白支架的GTP酶依赖性组装和解聚循环,并且涉及一个依赖于发动蛋白施加的曲率应力的随机过程。NT从支架释放后会自发发生裂变,且无泄漏。我们的计算表明,NT的局部变窄可诱导脂质协同倾斜,导致NT内单层的自我融合(半裂变),这与无泄漏现象一致。我们提出,发动蛋白将GTP的能量传递给有限曲率支架的周期性组装,该组装将脂质带到一个不稳定的中间体。

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