Exploring the relationships between protein sequence, structure and solubility

被引:54
|
作者
Trainor, Kyle [1 ]
Broom, Aron [1 ]
Meiering, Elizabeth M. [1 ]
机构
[1] Univ Waterloo, Dept Chem, 200 Univ Ave W, Waterloo, ON N2L 3G1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
ANTIBODY AGGREGATION; RATIONAL DESIGN; PREDICTION; EXPRESSION; MUTATIONS; SERVER; STABILITIES; LANDSCAPE; PEPTIDES; ENSEMBLE;
D O I
10.1016/j.sbi.2017.01.004
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
Aggregation can be thought of as a form of protein folding in which intermolecular associations lead to the formation of large, insoluble assemblies. Various types of aggregates can be differentiated by their internal structures and gross morphologies (e.g., fibrillar or amorphous), and the ability to accurately predict the likelihood of their formation by a given polypeptide is of great practical utility in the fields of biology (including the study of disease), biotechnology, and biomaterials research. Here we review aggregation/solubility prediction methods and selected applications thereof. The development of increasingly sophisticated methods that incorporate knowledge of conformations possibly adopted by aggregating polypeptide monomers and predict the internal structure of aggregates is improving the accuracy of the predictions and continually expanding the range of applications.
引用
收藏
页码:136 / 146
页数:11
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