State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.
Sci Rep. 2017 Apr 21;7:46569. doi: 10.1038/srep46569.
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.
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。