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The funnel approach to the precrystallization production of membrane proteins

机译:膜蛋白预结晶生产的漏斗方法

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Challenges in the production of integral membrane proteins for structural studies include low expression levels, incorrect membrane insertion, aggregation and instability. In this report, we describe a "funnel approach" to overcoming these difficulties and demonstrate its efficacy in a case study of 36 prokaryotic P-type transporters. A diverse ensemble of modified constructs is generated and tested for expression in Escherichia coli, membrane localization, detergent extraction, and homogeneity. High-throughput methodologies are implemented throughout the process to facilitate identification of promising targets. We find that the choice of promoter, the choice of source organism providing the cloned gene, and, most importantly, the position of the affinity tag have a great effect on successful production. The latter had pronounced effects at all tested levels, from expression levels observed in whole cells to the extent of membrane insertion, and even on protein function. Following the initial streamlined screening, we were able to fine-tune and produce 9 of the 36 targets as materials suitable for crystallization or other structural studies. (c) 2007 Elsevier Ltd. All rights reserved.
机译:用于结构研究的完整膜蛋白的生产挑战包括低表达水平,不正确的膜插入,聚集和不稳定性。在本报告中,我们描述了一种克服这些困难的“漏斗方法”,并在对36个原核P型转运蛋白的案例研究中证明了其有效性。产生了多种多样的修饰构建体集合,并对其在大肠杆菌中的表达,膜定位,去污剂提取和均质性进行了测试。在整个过程中都采用了高通量方法,以方便确定有希望的目标。我们发现启动子的选择,提供克隆基因的来源生物的选择以及最重要的是,亲和标签的位置对成功生产有很大影响。从在整个细胞中观察到的表达水平到膜插入的程度,甚至对蛋白质功能,后者在所有测试水平上都有明显的影响。经过最初的简化筛选,我们能够微调和生产36个靶中的9个,作为适合结晶或其他结构研究的材料。 (c)2007 Elsevier Ltd.保留所有权利。

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