巴马
细菌外膜
单克隆抗体
表位
整体膜蛋白
大肠杆菌
生物
细菌
木桶(钟表)
膜蛋白
细胞生物学
微生物学
抗体
生物化学
膜
免疫学
遗传学
基因
材料科学
复合材料
作者
Kelly M. Storek,Marcy R. Auerbach,Handuo Shi,Natalie K. Garcia,Dawei Sun,Nicholas N. Nickerson,Rajesh Vij,Zhonghua Lin,Nancy Chiang,Kellen Schneider,Aaron T. Wecksler,Elizabeth Skippington,Gerald R. Nakamura,Dhaya Seshasayee,James T. Koerber,Jian Payandeh,Peter A. Smith,Steven T. Rutherford
标识
DOI:10.1073/pnas.1800043115
摘要
Significance The outer membrane of Gram-negative bacteria presents a formidable barrier to the discovery of new antibiotics needed to combat infections by multidrug-resistant bacteria. Targeting essential proteins or processes directly exposed to the environment could bypass this obstacle. Here, we describe a monoclonal antibody that selectively and potently antagonizes BamA, which folds and inserts integral outer membrane β-barrel proteins, by binding to a surface-exposed BamA epitope and, as a result, inhibits bacterial cell growth. Mechanisms of resistance to the antibody reveal that membrane fluidity affects BamA activity. This antibody validates the potential therapeutic strategy of targeting essential, exposed functions and provides a powerful tool for dissecting the fundamental process of folding integral membrane β-barrel proteins in vivo.
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