Visualizing Protein Folding and Unfolding

被引:35
作者
Ferina, Jennifer [1 ]
Daggett, Valerie [1 ]
机构
[1] Univ Washington, Dept Bioengn, Box 355013, Seattle, WA 98195 USA
关键词
MOLECULAR-DYNAMICS SIMULATIONS; ENGRAILED HOMEODOMAIN; STRUCTURAL BASIS; SEQUENCE IDENTITY; DENATURED STATE; NUCLEIC-ACIDS; PATHWAY; MUTATIONS; NANOSECONDS; UBIQUITIN;
D O I
10.1016/j.jmb.2019.02.026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein folding/unfolding is a complicated process that defies high-resolution characterization by experimental methods. As an alternative, atomistic molecular dynamics simulations are now routinely employed to elucidate and magnify the accompanying conformational changes and the role of solvent in the folding process. However, the level of detail necessary to map the process at high spatial temporal resolution provides an overwhelming amount of data. As more and better tools are developed for analysis of these large data sets and validation of the simulations, one is still left with the problem of visualizing the results in ways that provide insight into the folding/unfolding process. While viewing and interrogating static crystal structures has become commonplace, more and different approaches are required for dynamic, interconverting, unfolding, and refolding proteins. Here we review a variety of approaches, ranging from straightforward to complex and unintuitive for multiscale analysis and visualization of protein folding and unfolding. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1540 / 1564
页数:25
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