Activity-based Tools for Interrogating Host Biology During Infection

被引:3
作者
Ramanathan, Renuka [1 ,2 ]
Hatzios, Stavroula K. [1 ,2 ,3 ]
机构
[1] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
[2] Yale Univ, Microbial Sci Inst, West Haven, CT 06516 USA
[3] Yale Univ, Dept Chem, New Haven, CT 06520 USA
关键词
Enzymes; proteomics; protein modifications; host-microbe interactions; infection; INNATE IMMUNITY; POSTTRANSLATIONAL MODIFICATIONS; SIGNAL-TRANSDUCTION; PLANT-PATHOGEN; PROTEIN; BACTERIAL; IDENTIFICATION; CONTRIBUTES; METABOLISM; TARGETS;
D O I
10.1002/ijch.202200095
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Host cells sense and respond to pathogens by dynamically regulating cell signaling. The rapid modulation of signaling pathways is achieved by post-translational modifications (PTMs) that can alter protein structure, function, and/or binding interactions. By using chemical probes to broadly profile changes in enzyme function or side-chain reactivity, activity-based protein profiling (ABPP) can reveal PTMs that regulate host-microbe interactions. While ABPP has been widely utilized to uncover microbial mechanisms of pathogenesis, in this review, we focus on more recent applications of this technique to the discovery of host PTMs and enzymes that modulate signaling within infected cells. Collectively, these advances underscore the importance of ABPP as a tool for interrogating the host response to infection and identifying potential targets for host-directed therapies.
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页数:13
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