An alliance between lipid transfer proteins and scramblases for membrane expansion.

Joost C M Holthuis, Helene Jahn, Anant K Menon, Noboru Mizushima
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引用次数: 2

Abstract

Membrane growth requires lipid supply, which is usually accomplished by lipid synthesis or vesicular trafficking. In the case of autophagosomes, these principles do not apply. Ghanbarpour et al. postulate that autophagosome expansion relies on non-vesicular lipid delivery from the ER, whereby the activity of a lipid transfer protein (LTP) is directly coupled to scramblase activities in the donor and acceptor bilayers1. This new concept opens the possibility that lipid traffic is controlled by scramblases that provide not only specific docking sites for LTPs, thereby directing lipid flow, but also support their activity by overcoming barriers for lipid extraction and deposition.

Abstract Image

脂质转移蛋白和超燃酶之间的膜扩张联盟。
膜生长需要脂质供应,通常通过脂质合成或囊泡运输来完成。在自噬体的情况下,这些原则不适用。Ghanbarpour等人假设自噬体的扩张依赖于内质网的非囊泡性脂质传递,因此脂质转移蛋白(LTP)的活性直接与供体和受体双分子层的促裂酶活性耦合1。这一新概念开启了一种可能性,即脂质运输是由扰流酶控制的,扰流酶不仅为ltp提供特定的对接位点,从而指导脂质流动,而且通过克服脂质提取和沉积的障碍来支持它们的活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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