低温电子显微
折叠(DSP实现)
多肽链
高分子
链条(单位)
独特性
结构生物学
结晶学
大分子物质
化学
生物物理学
计算生物学
计算机科学
物理
氨基酸
生物
生物化学
数学
工程类
数学分析
天文
电气工程
作者
Stavros Azinas,Marta Carroni
标识
DOI:10.1016/j.sbi.2023.102621
摘要
Cryogenic electron microscopy (cryo-EM) has become in the past 10 years one of the major tools for the structure determination of proteins. Nowadays, the structure prediction field is experiencing the same revolution and, using AlphaFold2, it is possible to have high-confidence atomic models for virtually any polypeptide chain, smaller than 4000 amino acids, in a simple click. Even in a scenario where all polypeptide chain folding were to be known, cryo-EM retains specific characteristics that make it a unique tool for the structure determination of macromolecular complexes. Using cryo-EM, it is possible to obtain near-atomic structures of large and flexible mega-complexes, describe conformational panoramas, and potentially develop a structural proteomic approach from fully ex vivo specimens.
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