核糖体
低温电子显微
计算生物学
结构生物学
核糖核酸
核糖体RNA
真核核糖体
计算机科学
生物
纳米技术
生物物理学
细胞生物学
遗传学
材料科学
基因
作者
Ottilie von Loeffelholz,S. Kundhavai Natchiar,Nadia Djabeur,Alexander G. Myasnikov,Hanna Kratzat,Jean‐François Ménétret,Isabelle Hazemann,Bruno P. Klaholz
标识
DOI:10.1016/j.sbi.2017.07.007
摘要
Cryo electron microscopy (cryo-EM) historically has had a strong impact on the structural and mechanistic analysis of protein synthesis by the prokaryotic and eukaryotic ribosomes. Vice versa, studying ribosomes has helped moving forwards many methodological aspects in single particle cryo-EM, at the level of automated data collection and image processing including advanced techniques for particle sorting to address structural and compositional heterogeneity. Here we review some of the latest ribosome structures, where cryo-EM allowed gaining unprecedented insights based on 3D structure sorting with focused classification and refinement methods helping to reach local resolution levels better than 3 Å. Such high-resolution features now enable the analysis of drug interactions with RNA and protein side-chains including even the visualization of chemical modifications of the ribosomal RNA. These advances represent a major breakthrough in structural biology and show the strong potential of cryo-EM beyond the ribosome field including for structure-based drug design.
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