Yang Yi, Song Haiping, Chen Peng R
Synthetic and Functional Biomolecules Center, Beijing National Laboratory for Molecular Sciences, Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry and Molecular Engineering, Peking University, Beijing, China.
Peking-Tsinghua Center for Life Sciences, Beijing, China.
IUBMB Life. 2016 Nov;68(11):879-886. doi: 10.1002/iub.1560. Epub 2016 Sep 26.
Protein-protein interactions (PPIs) play pivotal roles in regulation of many biological processes. Conventional methods are capable of investigating stable and strong interactions within protein complexes, but remain difficult for studying dynamic, transient, and weak PPIs. Herein we review photo-affinity unnatural amino acids that can be site-specifically incorporated into a protein of interest to covalently trap noncovalent PPIs under living conditions. A newly developed cleavable photocrosslinker from our group will also be introduced, which facilitated the prey-bait separation for better enrichment and identification of photocrosslinked PPI complexes. © 2016 IUBMB Life, 68(11):879-886, 2016.
蛋白质-蛋白质相互作用(PPIs)在许多生物过程的调控中起着关键作用。传统方法能够研究蛋白质复合物内部稳定且强烈的相互作用,但对于研究动态、瞬时和微弱的PPIs仍存在困难。在此,我们综述了光亲和性非天然氨基酸,其可位点特异性地掺入目标蛋白质中,以便在活细胞条件下共价捕获非共价PPIs。我们还将介绍本课题组新开发的一种可裂解的光交联剂,它有助于猎物-诱饵分离,从而更好地富集和鉴定光交联的PPI复合物。© 2016国际生物化学与分子生物学联盟生命科学部,68(11):879-886, 2016。