Saidijam Massoud, Benedetti Giulia, Ren Qinghu, Xu Zhiqiang, Hoyle Christopher J, Palmer Sarah L, Ward Alison, Bettaney Kim E, Szakonyi Gerda, Meuller Johan, Morrison Scott, Pos Martin K, Butaye Patrick, Walravens Karl, Langton Kate, Herbert Richard B, Skurray Ronald A, Paulsen Ian T, O'reilly John, Rutherford Nicholas G, Brown Melissa H, Bill Roslyn M, Henderson Peter J F
Astbury Centre for Structural Molecular Biology, School of Biochemistry and Microbiology, University of Leeds, Leeds LS2 9JT, UK.
Curr Drug Targets. 2006 Jul;7(7):793-811. doi: 10.2174/138945006777709575.
Drug efflux proteins are widespread amongst microorganisms, including pathogens. They can contribute to both natural insensitivity to antibiotics and to emerging antibiotic resistance and so are potential targets for the development of new antibacterial drugs. The design of such drugs would be greatly facilitated by knowledge of the structures of these transport proteins, which are poorly understood, because of the difficulties of obtaining crystals of quality. We describe a structural genomics approach for the amplified expression, purification and characterisation of prokaryotic drug efflux proteins of the 'Major Facilitator Superfamily' (MFS) of transport proteins from Helicobacter pylori, Staphylococcus aureus, Escherichia coli, Enterococcus faecalis, Bacillus subtilis, Brucella melitensis, Campylobacter jejuni, Neisseria meningitides and Streptomyces coelicolor. The H. pylori putative drug resistance protein, HP1092, and the S. aureus QacA proteins are used as detailed examples. This strategy is an important step towards reproducible production of transport proteins for the screening of drug binding and for optimisation of crystallisation conditions to enable subsequent structure determination.
药物外排蛋白广泛存在于包括病原体在内的微生物中。它们既可能导致对抗生素的天然不敏感性,也可能促使新的抗生素耐药性产生,因此是开发新型抗菌药物的潜在靶点。了解这些转运蛋白的结构将极大地推动此类药物的设计,但由于难以获得高质量晶体,目前对此类蛋白的了解还很有限。我们描述了一种结构基因组学方法,用于对来自幽门螺杆菌、金黄色葡萄球菌、大肠杆菌、粪肠球菌、枯草芽孢杆菌、羊布鲁氏菌、空肠弯曲菌、脑膜炎奈瑟菌和天蓝色链霉菌的“主要易化子超家族”(MFS)转运蛋白中的原核药物外排蛋白进行扩增表达、纯化和表征。以幽门螺杆菌假定的耐药蛋白HP1092和金黄色葡萄球菌QacA蛋白为例进行详细说明。该策略是朝着可重复生产转运蛋白迈出的重要一步,有助于筛选药物结合情况并优化结晶条件,以便后续确定结构。