4.5 Review

Multiscale simulation approaches to modeling drug-protein binding

期刊

CURRENT OPINION IN STRUCTURAL BIOLOGY
卷 61, 期 -, 页码 213-221

出版社

CURRENT BIOLOGY LTD
DOI: 10.1016/j.sbi.2020.01.014

关键词

-

资金

  1. EPSRC [EP/M015378/1, EP/M022609/1]
  2. National Biomedical Computation Resource (NBCR) [P41-GM103426]
  3. NIH Molecular Biophysics Training Program [T32-GM008326]

向作者/读者索取更多资源

Simulations can provide detailed insight into the molecular processes involved in drug action, such as protein-ligand binding, and can therefore be a valuable tool for drug design and development. Processes with a large range of length and timescales may be involved, and understanding these different scales typically requires different types of simulation methodology. Ideally, simulations should be able to connect across scales, to analyze and predict how changes at one scale can influence another. Multiscale simulation methods, which combine different levels of treatment, are an emerging frontier with great potential in this area. Here we review multiscale frameworks of various types, and selected applications to biomolecular systems with a focus on drug-ligand binding.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据