Enzyme-targeted fluorescent small-molecule probes for bacterial imaging

被引:25
|
作者
Marshall, Andrew P. [1 ]
Shirley, Joshua D. [2 ]
Carlson, Erin E. [1 ,2 ,3 ]
机构
[1] Univ Minnesota, Dept Chem, 207 Pleasant St SE, 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
基金
美国国家卫生研究院;
关键词
Bacteria; Fluorescence imaging; Chemical probe; Electrophile; Activity-based probe; PENICILLIN-BINDING PROTEINS; BETA-LACTAM SELECTIVITY; CELL BIOLOGY; IDENTIFICATION; DISCOVERY; DYNAMICS; TRACKING; TOOLS; GFP;
D O I
10.1016/j.cbpa.2020.05.012
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
Molecular imaging methods to visualize myriad biochemical processes in bacteria have traditionally been dependent upon molecular biology techniques to incorporate fluorescent biomolecules (e.g., fusion proteins). Such methods have been instrumental in our understanding of how bacteria function but are not without drawbacks, including potential perturbation to native protein expression and function. To overcome these limitations, the use of fluorescent small-molecule probes has gained much attention. Here, we highlight examples from the recent literature that showcase the utility of small-molecule probes for the fluorescence imaging of bacterial cells, including electrophilic, metabolic, and enzyme-activated probes. Although the use of these types of compounds for bacterial imaging is still relatively new, the selected examples demonstrate the exciting potential of these critical tools in the exploration of bacterial physiology.
引用
收藏
页码:155 / 165
页数:11
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