详细信息
Conformational dynamics of the MdfA multidrug efflux pump and structural mechanisms underlying substrate efflux: A review ( SCI-EXPANDED收录 EI收录)
文献类型:期刊文献
英文题名:Conformational dynamics of the MdfA multidrug efflux pump and structural mechanisms underlying substrate efflux: A review
作者:Xue, Xiaozhou[1,2];Sun, Huijie[1];Li, Ying[1]
第一作者:Xue, Xiaozhou
通讯作者:Li, Y[1]
机构:[1]Beijing Union Univ, Coll Biochem Engn, Beijing 100023, Peoples R China;[2]SDIC Biotechnol Investment Co Ltd, Beijing 100034, Peoples R China
第一机构:北京联合大学生物化学工程学院
通讯机构:[1]corresponding author), Beijing Union Univ, Coll Biochem Engn, Beijing 100023, Peoples R China.|[1141726]北京联合大学生物化学工程学院;[11417]北京联合大学;
年份:2026
卷号:347
外文期刊名:INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
收录:;EI(收录号:20260620036358);WOS:【SCI-EXPANDED(收录号:WOS:001689698300004)】;
基金:This work is financially supported by the Project of Cultivation for Young Top-notch Talents of Beijing Municipal Institutions (BPHR202203209) .
语种:英文
外文关键词:MdfA; Multidrug efflux pump; Conformational dynamics; Antibiotic resistance
摘要:The multidrug efflux pump MdfA, a prototypical member of the Major Facilitator Superfamily (MFS), plays a pivotal role in antibiotic resistance in Escherichia coli by exporting a remarkably broad spectrum of structurally diverse compounds. Despite extensive structural characterization, a unified mechanistic framework linking MdfA's conformational dynamics to substrate recognition and proton-coupled antiport remains incomplete. In this review, we synthesize current knowledge on MdfA with a focus on the conformational transitions underlying multidrug efflux. We compare available inward-and outward-facing structures and critically assess representative models of conformational change in MFS transporters. Experimental evidence from crystallography, mutagenesis, and biophysical assays is integrated with molecular dynamics simulations and AI-assisted structural predictions to capture functional motions beyond static structures. In addition, analysis of known substrates and inhibitors reveals conserved elements essential for proton coupling and variable regions enabling substrate polyspecificity. We further discuss how insights into MdfA's conformational landscape inform emerging strategies for efflux pump inhibition and multidrug resistance. Collectively, this review establishes a mechanistically unified framework that links structure, dynamics, and function, providing generalizable principles for understanding and targeting multidrug transporters across the MFS family.
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