铜绿假单胞菌
细菌外膜
头孢他啶
生物物理学
细菌
膜
基质(水族馆)
化学
生物
生物化学
大肠杆菌
基因
遗传学
生态学
作者
Susruta Samanta,Igor Bodrenko,Silvia Acosta‐Gutiérrez,Tommaso D’Agostino,M. Pathania,Ishan Ghai,Christian Schleberger,Dirk Bumann,Richard Wagner,Mathias Winterhalter,Bert van den Berg,Matteo Ceccarelli
标识
DOI:10.1021/acsinfecdis.8b00149
摘要
Understanding molecular properties of outer membrane channels of Gram-negative bacteria is of fundamental significance as they are the entry point of polar antibiotics into bacteria. Outer membrane proteomics revealed OccK8 (OprE) to be among the five most expressed substrate specific channels of the clinically important Pseudomonas aeruginosa. The high-resolution X-ray structure and electrophysiology highlighted a very narrow pore. However, experimental in vitro methods showed the transport of natural amino acids and antibiotics, among them ceftazidime. We used molecular dynamics simulations to reveal the importance of the physicochemical properties of ceftazidime in modulating the translocation through OccK8, proposing a structure-function relationship. As in general porins, the internal electric field favors the translocation of polar molecules by gainful energy compensation in the central constriction region. Importantly, the comparatively narrow OccK8 pore can undergo a substrate-induced expansion to accommodate relatively large-sized substrates.
科研通智能强力驱动
Strongly Powered by AbleSci AI