Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Department of Chemistry, Bridge Institute, University of Southern California, Los Angeles, CA 90089, USA.
Curr Opin Struct Biol. 2019 Oct;58:278-285. doi: 10.1016/j.sbi.2019.06.002. Epub 2019 Jul 5.
Solving high-resolution structures of membrane proteins has been an important challenge for decades, still lagging far behind that of soluble proteins even with the recent remarkable technological advances in X-ray crystallography and electron microscopy. Central to this challenge is the necessity to isolate and solubilize membrane proteins in a stable, natively folded and functional state, a process influenced by not only the proteins but also their surrounding chemical environment. This review highlights recent community efforts in the development and characterization of novel membrane agents and ligand tools to stabilize individual proteins and protein complexes, which together have accelerated progress in membrane protein structural biology.
解析膜蛋白的高分辨率结构是数十年来的重要挑战,即使在 X 射线晶体学和电子显微镜技术最近取得显著进步的情况下,其进展仍远远落后于可溶性蛋白。这一挑战的核心是需要将膜蛋白在稳定、天然折叠和功能状态下进行分离和溶解,这一过程不仅受到蛋白质的影响,还受到其周围化学环境的影响。本文重点介绍了社区最近在开发和表征新型膜试剂和配体工具以稳定单个蛋白质和蛋白质复合物方面的努力,这些努力共同加速了膜蛋白结构生物学的进展。