Structure determination of an integral membrane protein at room temperature from crystals in situ.

Danny Axford, James Foadi, Nien Jen Hu, Hassanul Ghani Choudhury, So Iwata, Konstantinos Beis, Gwyndaf Evans, Yilmaz Alguel
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Abstract

The structure determination of an integral membrane protein using synchrotron X-ray diffraction data collected at room temperature directly in vapour-diffusion crystallization plates (in situ) is demonstrated. Exposing the crystals in situ eliminates manual sample handling and, since it is performed at room temperature, removes the complication of cryoprotection and potential structural anomalies induced by sample cryocooling. Essential to the method is the ability to limit radiation damage by recording a small amount of data per sample from many samples and subsequently assembling the resulting data sets using specialized software. The validity of this procedure is established by the structure determination of Haemophilus influenza TehA at 2.3 Å resolution. The method presented offers an effective protocol for the fast and efficient determination of membrane-protein structures at room temperature using third-generation synchrotron beamlines.

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利用原位晶体确定整体膜蛋白在室温下的结构。
演示了利用同步辐射 X 射线衍射数据在室温下直接在蒸汽扩散结晶板(原位)中采集的积分膜蛋白的结构测定。原位曝光晶体无需人工处理样品,由于是在室温下进行,因此消除了样品低温冷却引起的低温保护和潜在结构异常的复杂性。该方法的关键在于能够限制辐射损伤,即从许多样品中为每个样品记录少量数据,然后使用专用软件将得到的数据集组合起来。通过对流感嗜血杆菌 TehA 进行 2.3 Å 分辨率的结构测定,证明了该方法的有效性。所介绍的方法为利用第三代同步辐射光束线在室温下快速、高效地测定膜蛋白结构提供了有效的方案。
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