Straub Monique S, Harder Oliver F, Mowry Nathan J, Barrass Sarah V, Hruby Jakub, Drabbels Marcel, Lorenz Ulrich J
Ecole Polytechnique Fédérale de Lausanne (EPFL), Laboratory of Molecular Nanodynamics, CH-1015 Lausanne, Switzerland.
bioRxiv. 2024 Nov 21:2024.11.21.624652. doi: 10.1101/2024.11.21.624652.
Sample preparation remains a bottleneck for protein structure determination by cryo-electron microscopy. A frequently encountered issue is that proteins adsorb to the air-water interface of the sample in a limited number of orientations. This makes it challenging to obtain high-resolution reconstructions or may even cause projects to fail altogether. We have previously observed that laser flash melting and revitrification of cryo samples reduces preferred orientation for large, symmetric particles. Here, we demonstrate that our method can in fact be used to scramble the orientation of proteins of a range of sizes and symmetries. The effect can be enhanced for some proteins by increasing the heating rate during flash melting or by depositing amorphous ice onto the sample prior to revitrification. This also allows us to shed light onto the underlying mechanism. Our experiments establish a set of tools for overcoming preferred orientation that can be easily integrated into existing workflows.
样品制备仍然是通过冷冻电子显微镜确定蛋白质结构的一个瓶颈。一个经常遇到的问题是,蛋白质会以有限的几种取向吸附到样品的空气-水界面上。这使得获得高分辨率的重建结果具有挑战性,甚至可能导致项目完全失败。我们之前观察到,冷冻样品的激光闪光熔化和再玻璃化可以减少大型对称颗粒的择优取向。在这里,我们证明我们的方法实际上可用于扰乱一系列大小和对称性的蛋白质的取向。对于某些蛋白质,通过在闪光熔化过程中提高加热速率或在再玻璃化之前在样品上沉积非晶冰,可以增强这种效果。这也使我们能够深入了解潜在机制。我们的实验建立了一套克服择优取向的工具,这些工具可以很容易地整合到现有的工作流程中。