Biocomputing Unit, Centro Nac. Biotecnología (CSIC), Cantoblanco, Madrid, Spain.
UMR CNRS 7590, Muséum National d ´Histoire Naturelle, IRD, Institut de Minéralogie, de Physique des Matériaux et de Cosmochimie, IMPMC, Sorbonne Université, Paris, France.
Bioinformatics. 2019 Jul 15;35(14):2427-2433. doi: 10.1093/bioinformatics/bty985.
Cryo electron microscopy (EM) is currently one of the main tools to reveal the structural information of biological macromolecules. The re-construction of three-dimensional (3D) maps is typically carried out following an iterative process that requires an initial estimation of the 3D map to be refined in subsequent steps. Therefore, its determination is key in the quality of the final results, and there are cases in which it is still an open issue in single particle analysis (SPA). Small angle X-ray scattering (SAXS) is a well-known technique applied to structural biology. It is useful from small nanostructures up to macromolecular ensembles for its ability to obtain low resolution information of the biological sample measuring its X-ray scattering curve. These curves, together with further analysis, are able to yield information on the sizes, shapes and structures of the analyzed particles.
In this paper, we show how the low resolution structural information revealed by SAXS is very useful for the validation of EM initial 3D models in SPA, helping the following refinement process to obtain more accurate 3D structures. For this purpose, we approximate the initial map by pseudo-atoms and predict the SAXS curve expected for this pseudo-atomic structure. The match between the predicted and experimental SAXS curves is considered as a good sign of the correctness of the EM initial map.
The algorithm is freely available as part of the Scipion 1.2 software at http://scipion.i2pc.es/.
冷冻电子显微镜(Cryo EM)目前是揭示生物大分子结构信息的主要工具之一。三维(3D)地图的重建通常是通过一个迭代过程进行的,这个过程需要对 3D 地图进行初步估计,然后在后续步骤中进行细化。因此,其确定是最终结果质量的关键,在单颗粒分析(SPA)中,有些情况下它仍然是一个未解决的问题。小角 X 射线散射(Small angle X-ray scattering,SAXS)是一种应用于结构生物学的知名技术。它适用于从小纳米结构到大分子集合体,因为它能够通过测量生物样品的 X 射线散射曲线来获取低分辨率的生物样品信息。这些曲线与进一步的分析一起,可以提供关于分析粒子的大小、形状和结构的信息。
在本文中,我们展示了 SAXS 揭示的低分辨率结构信息如何有助于 SPA 中 EM 初始 3D 模型的验证,从而帮助后续的细化过程获得更准确的 3D 结构。为此,我们通过拟原子来逼近初始地图,并预测这个拟原子结构的预期 SAXS 曲线。预测和实验 SAXS 曲线之间的匹配被认为是 EM 初始地图正确性的良好标志。
该算法作为 Scipion 1.2 软件的一部分免费提供,可在 http://scipion.i2pc.es/ 获得。