In meso in situ serial X-ray crystallography of soluble and membrane proteins.

Chia Ying Huang, Vincent Olieric, Pikyee Ma, Ezequiel Panepucci, Kay Diederichs, Meitian Wang, Martin Caffrey
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引用次数: 99

Abstract

The lipid cubic phase (LCP) continues to grow in popularity as a medium in which to generate crystals of membrane (and soluble) proteins for high-resolution X-ray crystallographic structure determination. To date, the PDB includes 227 records attributed to the LCP or in meso method. Among the listings are some of the highest profile membrane proteins, including the β2-adrenoreceptor-Gs protein complex that figured in the award of the 2012 Nobel Prize in Chemistry to Lefkowitz and Kobilka. The most successful in meso protocol to date uses glass sandwich crystallization plates. Despite their many advantages, glass plates are challenging to harvest crystals from. However, performing in situ X-ray diffraction measurements with these plates is not practical. Here, an alternative approach is described that provides many of the advantages of glass plates and is compatible with high-throughput in situ measurements. The novel in meso in situ serial crystallography (IMISX) method introduced here has been demonstrated with AlgE and PepT (alginate and peptide transporters, respectively) as model integral membrane proteins and with lysozyme as a test soluble protein. Structures were solved by molecular replacement and by experimental phasing using bromine SAD and native sulfur SAD methods to resolutions ranging from 1.8 to 2.8 Å using single-digit microgram quantities of protein. That sulfur SAD phasing worked is testament to the exceptional quality of the IMISX diffraction data. The IMISX method is compatible with readily available, inexpensive materials and equipment, is simple to implement and is compatible with high-throughput in situ serial data collection at macromolecular crystallography synchrotron beamlines worldwide. Because of its simplicity and effectiveness, the IMISX approach is likely to supplant existing in meso crystallization protocols. It should prove particularly attractive in the area of ligand screening for drug discovery and development.

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可溶性蛋白和膜蛋白的介观原位连续x射线晶体学。
脂质立方相(LCP)作为一种生成膜(和可溶性)蛋白质晶体的介质,用于高分辨率x射线晶体学结构测定,越来越受欢迎。迄今为止,PDB包括227条属于LCP或meso方法的记录。在这些名单中,有一些最引人注目的膜蛋白,包括β2-肾上腺素受体- gs蛋白复合物,它被授予2012年诺贝尔化学奖给莱夫科维茨和科比尔卡。迄今为止,最成功的中观方案是使用玻璃夹层结晶板。尽管玻璃板有许多优点,但从中收集晶体是一项挑战。然而,用这些板进行原位x射线衍射测量是不实际的。在这里,描述了一种替代方法,它提供了玻璃板的许多优点,并且与高通量原位测量兼容。本文介绍了以AlgE和PepT(分别为海藻酸盐和肽转运蛋白)为模型整体膜蛋白,以溶菌酶为测试可溶性蛋白的新型中位连续晶体学(IMISX)方法。结构通过分子替代和实验分相解决,使用溴SAD和天然硫SAD方法,分辨率范围从1.8到2.8 Å,使用单位微克量的蛋白质。硫SAD相位工作证明了IMISX衍射数据的卓越质量。IMISX方法与现成的廉价材料和设备兼容,易于实施,并且与世界各地大分子晶体同步加速器光束线的高通量原位串行数据收集兼容。由于其简单和有效,IMISX方法很可能取代现有的介观结晶方法。它在药物发现和开发的配体筛选领域应该特别有吸引力。
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