Skach William R
William R Skach is in the Department of Biochemistry & Molecular Biology, Oregon Health & Sciences University, Portland, Oregon, USA.
Nat Struct Mol Biol. 2009 Jun;16(6):606-12. doi: 10.1038/nsmb.1600.
The membrane protein-folding problem can be articulated by two central questions. How is protein topology established by selective peptide transport to opposite sides of the cellular membrane? And how are transmembrane segments inserted, integrated and folded within the lipid bilayer? In eukaryotes, this process usually takes place in the endoplasmic reticulum, coincident with protein synthesis, and is facilitated by the translating ribosome and the Sec61 translocon complex (RTC). At its core, the RTC forms a dynamic pathway through which the elongating nascent polypeptide moves as it is delivered into the cytosolic, lumenal and lipid compartments. This Perspective will focus on emerging evidence that the RTC functions as a protein-folding machine that restricts conformational space by establishing transmembrane topology and yet provides a permissive environment that enables nascent transmembrane domains to efficiently progress down their folding energy landscape.
膜蛋白折叠问题可以通过两个核心问题来阐述。蛋白质拓扑结构是如何通过选择性肽转运到细胞膜的相对两侧而建立的?跨膜片段又是如何在脂质双分子层中插入、整合和折叠的?在真核生物中,这个过程通常在内质网中与蛋白质合成同时发生,并由正在翻译的核糖体和Sec61转运体复合物(RTC)促进。其核心是,RTC形成了一条动态途径,正在延长的新生多肽在被输送到胞质、腔和脂质区室时通过该途径移动。本综述将聚焦于新出现的证据,即RTC作为一种蛋白质折叠机器,通过建立跨膜拓扑结构来限制构象空间,但同时提供一个宽松的环境,使新生跨膜结构域能够有效地沿着其折叠能量景观前进。