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脂肪酸合酶与 protrudin 合作促进细胞突起的膜延伸。

Fatty acid synthase cooperates with protrudin to facilitate membrane outgrowth of cellular protrusions.

机构信息

State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.

出版信息

Sci Rep. 2017 Apr 21;7:46569. doi: 10.1038/srep46569.

Abstract

Cellular protrusion formation capacity is a key feature of developing neurons and many eukaryotic cells. However, the mechanisms underlying membrane growth in protrusion formation are largely unclear. In this study, photo-reactive unnatural amino acid 3-(3-methyl-3H-diazirin-3-yl)-propamino-carbonyl-Nε-l-lysine was incorporated by a genetic code expansion strategy into protrudin, a protein localized in acidic endosomes and in the endoplasmic reticulum, that induces cellular protrusion and neurite formation. The modified protrudin was used for covalent trapping of protrudin-interacting proteins in living cells. Fatty acid synthase (FASN), which synthesizes free fatty acids, was identified to transiently interact with protrudin. Further characterization revealed a unique cooperation mechanism in which protrudin cooperates with FASN to facilitate cellular protrusion formation. This work reveals a novel mechanism involved in protrusion formation that is dependent on transient interaction between FASN and protrudin, and establishes a creative strategy to investigate transient protein-protein interactions in mammalian cells.

摘要

细胞突起形成能力是发育神经元和许多真核细胞的关键特征。然而,突起形成中膜生长的机制在很大程度上尚不清楚。在这项研究中,通过遗传密码扩展策略将光反应性非天然氨基酸 3-(3-甲基-3H-二氮杂环丁-3-基)丙氨酰-Nε-l-赖氨酸掺入定位于酸性内涵体和内质网中的突起蛋白中,该蛋白诱导细胞突起和神经突形成。修饰后的突起蛋白用于活细胞中突起蛋白相互作用蛋白的共价捕获。鉴定出合成游离脂肪酸的脂肪酸合酶(FASN)与突起蛋白瞬时相互作用。进一步的表征揭示了一种独特的合作机制,其中突起蛋白与 FASN 合作促进细胞突起形成。这项工作揭示了一种新的突起形成机制,该机制依赖于 FASN 和突起蛋白之间的瞬时相互作用,并建立了一种创新策略来研究哺乳动物细胞中瞬时的蛋白质-蛋白质相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f83f/5399442/9e3e1226a0de/srep46569-f1.jpg

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