灵活性(工程)
计算生物学
抗体
蛋白质结构
计算机科学
结构生物学
低温电子显微
纳米技术
化学
生物物理学
生物
材料科学
免疫学
生物化学
数学
统计
作者
Dongjun Guo,Maria Laura De Sciscio,Joseph Ng,Franca Fraternali
标识
DOI:10.1016/j.sbi.2023.102757
摘要
Antibodies are large protein assemblies capable of both specifically recognising antigens and engaging with other proteins and receptors to coordinate immune action. Traditionally, structural studies have been dedicated to antibody variable regions, but efforts to determine and model full-length antibody structures are emerging. Here we review the current knowledge on modelling the structures of antibody assemblies, focusing on their conformational flexibility and the challenge this poses to obtaining and evaluating structural models. Integrative modelling approaches, combining experiments (cryo-electron microscopy, mass spectrometry, etc.) and computational methods (molecular dynamics simulations, deep-learning based approaches, etc.), hold the promise to map the complex conformational landscape of full-length antibody structures.
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