Department of Biophysics and Radiation Biology, Semmelweis University, Budapest 1094, Hungary.
MTA-SE Molecular Biophysics Research Group, Hungarian Academy of Sciences, Budapest 1094, Hungary.
Bioinformatics. 2020 Apr 15;36(8):2595-2598. doi: 10.1093/bioinformatics/btz539.
The identification of transmembrane helices in transmembrane proteins is crucial, not only to understand their mechanism of action but also to develop new therapies. While experimental data on the boundaries of membrane-embedded regions are sparse, this information is present in cryo-electron microscopy (cryo-EM) density maps and it has not been utilized yet for determining membrane regions. We developed a computational pipeline, where the inputs of a cryo-EM map, the corresponding atomistic structure, and the potential bilayer orientation determined by TMDET algorithm of a given protein result in an output defining the residues assigned to the bulk water phase, lipid interface and the lipid hydrophobic core. Based on this method, we built a database involving published cryo-EM protein structures and a server to be able to compute this data for newly obtained structures.
Supplementary data are available at Bioinformatics online.
鉴定跨膜蛋白中的跨膜螺旋至关重要,不仅要了解其作用机制,还要开发新的治疗方法。虽然关于膜嵌入区域边界的实验数据很少,但这些信息存在于冷冻电子显微镜(cryo-EM)密度图中,尚未用于确定膜区域。我们开发了一种计算管道,其中输入是 cryo-EM 图谱、相应的原子结构以及由给定蛋白质的 TMDET 算法确定的潜在双层取向,输出定义分配给主体水相、脂质界面和脂质疏水区的残基。基于该方法,我们构建了一个包含已发表的 cryo-EM 蛋白质结构的数据库,并构建了一个服务器,以便能够为新获得的结构计算这些数据。
补充数据可在 Bioinformatics 在线获得。