Emerging technologies in protein interface engineering for biomedical applications

被引:5
作者
Krohl, Patrick J. [1 ]
Ludwig, Seth D. [1 ]
Spangler, Jamie B. [1 ,2 ]
机构
[1] Johns Hopkins Univ, Dept Chem & Biomol Engn, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD 21218 USA
关键词
ERYTHROPOIETIN RECEPTOR; COMPUTATIONAL DESIGN; SIGNAL-TRANSDUCTION; PATHWAYS; INTERLEUKIN-2; SPECIFICITY; SELECTIVITY; INHIBITOR; BIOLOGY; IL-2;
D O I
10.1016/j.copbio.2019.01.017
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Protein interactions communicate critical information from the environment into cells to orchestrate functional responses relevant to health and disease. Whereas the natural repertoire of protein interfaces is finite, biomolecular engineering tools provide access to an unlimited scope of potential interactions that can be custom-designed for affinity, specificity, mechanism, or other properties of interest. This review highlights recent developments in protein interface engineering that offer insight into human physiology to inform the design of new pharmaceuticals, with a particular focus on immunotherapeutics. We cover three innovative and translationally promising approaches: ( I) reprogramming receptor oligomerization to manipulate signaling pathways; (2) computational protein interface design strategies; and (3) engineering bioorthogonal protein interaction networks.
引用
收藏
页码:82 / 88
页数:7
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