Activity-based probes in pathogenic bacteria: Investigating drug targets and molecule specificity

被引:1
|
作者
Lembke, Hannah K. [1 ]
Carlson, Erin E. [1 ,2 ,3 ,4 ]
机构
[1] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Med Chem, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Dept Biochem Mol Biol & Biophys, Minneapolis, MN 55455 USA
[4] Univ Minnesota, Dept Pharmacol, Minneapolis, MN 55455 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Bacterial pathogens; Antibiotics; Activity-based probes; STRATEGIES; INHIBITORS; UREAS;
D O I
10.1016/j.cbpa.2023.102359
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
Bacteria comprise complex communities within our bodies and largely have beneficial roles, however a small percentage are pathogenic. While all pathogens are important to public health, immediate action is necessary to combat bacterial strains developing pan- and multi-resistance to antibiotics. As present therapeutics fail to tackle this problem, novel strategies are required to address this threat. Activity-based probes (ABPs) are one method to investigate proteins of interest in pathogens. These probes can serve multiple purposes to better our understanding of bacterial pathogenicity. Herein, we highlight recent studies that used ABPs to identify new drug targets or visualize antibiotic resistance- or bacterial virulenceassociated proteins, and introduce strategies to determine the specificity of ABPs within a targeted enzyme class.
引用
收藏
页数:8
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