School of Cellular and Molecular Medicine, Medical Sciences Building, University of Bristol, University Walk BS8 1TD, United Kingdom.
J Struct Biol. 2013 Apr;182(1):51-6. doi: 10.1016/j.jsb.2013.01.004. Epub 2013 Jan 26.
Difficulties associated with using X-ray crystallography for structural studies of large macromolecular complexes have made single particle cryo-electron microscopy (cryoEM) a key technique in structural biology. The efficient application of the single particle cryoEM approach requires the sample to be vitrified within the holes of carbon films, with particles well dispersed throughout the ice and adopting multiple orientations. To achieve this, the carbon support film is first hydrophilised by glow discharge, which allows the sample to spread over the film. Unfortunately, for transmembrane complexes especially, this procedure can result in severe sample adsorption to the carbon support film, reducing the number of particles dispersed in the ice. This problem is rate-limiting in the single particle cryoEM approach and has hindered its widespread application to hydrophobic complexes. We describe a novel grid preparation technique that allows for good particle dispersion in the ice and minimal hydrophobic particle adhesion to the support film. This is achieved by hydrophilisation of the carbon support film by the use of selected detergents that interact with the support so as to achieve a hydrophilic and neutral or selectively charged surface.
使用 X 射线晶体学进行大型大分子复合物结构研究的困难使得单颗粒冷冻电子显微镜(cryoEM)成为结构生物学中的关键技术。单颗粒 cryoEM 方法的有效应用要求样品在碳膜的孔内形成玻璃态,颗粒在冰中均匀分散并采用多种取向。为此,首先通过辉光放电使碳支撑膜亲水,从而使样品在膜上展开。不幸的是,对于跨膜复合物特别是这样,该过程会导致样品严重吸附到碳支撑膜上,从而减少了分散在冰中的颗粒数量。这个问题是单颗粒 cryoEM 方法的限速步骤,阻碍了其在疏水性复合物中的广泛应用。我们描述了一种新颖的网格制备技术,该技术允许在冰中良好分散颗粒,并且支持膜上的疏水性颗粒粘附最小化。这是通过使用与支撑膜相互作用的选定去污剂使碳支撑膜亲水,并实现亲水且中性或选择性带电的表面来实现的。