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深入了解 VPS13 的特性和功能揭示了真核生物脂质运输的新机制。

Insights into VPS13 properties and function reveal a new mechanism of eukaryotic lipid transport.

机构信息

Department of Neuroscience, Howard Hughes Medical Institute, Program in Cellular Neuroscience, Neurodegeneration and Repair, Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, USA; Department of Cell Biology, Yale School of Medicine, New Haven, CT, USA; Aligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, USA; CNR Institute of Neuroscience, Milan, Italy and Humanitas Clinical and Research Center, Rozzano, MI, Italy.

Department of Cell Biology, Yale School of Medicine, New Haven, CT, USA; Aligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, USA.

出版信息

Biochim Biophys Acta Mol Cell Biol Lipids. 2021 Oct;1866(10):159003. doi: 10.1016/j.bbalip.2021.159003. Epub 2021 Jul 1.

Abstract

The occurrence of protein mediated lipid transfer between intracellular membranes has been known since the late 1960's. Since these early discoveries, numerous proteins responsible for such transport, which often act at membrane contact sites, have been identified. Typically, they comprise a lipid harboring module thought to shuttle back and forth between the two adjacent bilayers. Recently, however, studies of the chorein domain protein family, which includes VPS13 and ATG2, has led to the identification of a novel mechanism of lipid transport between organelles in eukaryotic cells mediated by a rod-like protein bridge with a hydrophobic groove through which lipids can slide. This mechanism is ideally suited for bulk transport of bilayer lipids to promote membrane growth. Here we describe how studies of VPS13 led to the discovery of this new mechanism, summarize properties and known roles of VPS13 proteins, and discuss how their dysfunction may lead to disease.

摘要

自 20 世纪 60 年代末以来,人们就已经知道细胞内膜之间存在蛋白质介导的脂质转移。自这些早期发现以来,已经鉴定出许多负责这种运输的蛋白质,这些蛋白质通常在膜接触位点发挥作用。通常,它们包含一个脂质结合模块,被认为在两个相邻的双层膜之间来回穿梭。然而,最近对 chorein 结构域蛋白家族(包括 VPS13 和 ATG2)的研究,导致了一种新的脂质运输机制的鉴定,该机制由一个杆状蛋白桥介导,该蛋白桥带有一个疏水槽,脂质可以在其中滑动。这种机制非常适合双层脂质的批量运输,以促进膜生长。在这里,我们描述了 VPS13 的研究如何导致这一新机制的发现,总结了 VPS13 蛋白的特性和已知作用,并讨论了它们的功能障碍如何导致疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c51c/8325632/330f7c7a4228/nihms-1723272-f0001.jpg

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