首页> 美国卫生研究院文献>Acta Crystallographica Section F: Structural Biology and Crystallization Communications >Expression, purification, crystallization and preliminary X-ray studies of the outer membrane efflux proteins OprM and OprN from Pseudomonas aeruginosa
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Expression, purification, crystallization and preliminary X-ray studies of the outer membrane efflux proteins OprM and OprN from Pseudomonas aeruginosa

机译:铜绿假单胞菌外膜外排蛋白OprM和OprN的表达,纯化,结晶和初步X射线研究

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摘要

OprM and OprN belong to the outer membrane factor family proteins. These ∼52 kDa proteins are part of the tripartite efflux pumps found in Pseudomonas aeruginosa and are responsible in part for the antibiotic resistance observed in these bacteria. Both proteins have been expressed in Escherichia coli as His-tag proteins and purified accordingly by affinity chromatography in the presence of n-octyl-β-d-glucopyranoside detergent. OprM and OprN were crystallized using PEG 20 000/ammonium citrate and ammonium sulfate as precipitating agents, respectively. Crystals belong to space group C2, with unit-cell parameters a = 152.6, b = 87.9, c = 355.9 Å, β = 98.9° and a = 151.3, b = 87.6, c = 356.5 Å, β = 98.1° for OprM and OprN, respectively. Using the ESRF synchrotron-radiation source, OprM diffraction data extended to 3.4 Å.
机译:OprM和OprN属于外膜因子家族蛋白。这些约52kkDa的蛋白质是在铜绿假单胞菌中发现的三方外排泵的一部分,部分负责这些细菌中观察到的抗生素抗性。两种蛋白均已在大肠杆菌中表达为His-tag蛋白,​​并在存在正辛基-β-d-吡喃葡萄糖苷去污剂的情况下通过亲和色谱法进行了相应纯化。 OprM和OprN分别使用PEG 20 000 /柠檬酸铵和硫酸铵作为沉淀剂进行结晶。晶体属于C2空间群,其晶胞参数a = 152.6,b = 87.9,c = 355.9,β= 98.9°和a = 151.3,b = 87.6,c = 356.5,对于OprM和β= 98.1°分别为OprN。使用ESRF同步加速器辐射源,OprM衍射数据扩展到3.4Å。

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