Recent advances in high-throughput screening methods for small molecule modulators in bacteria

被引:0
|
作者
Addis, Hannah G. [1 ]
Carlson, Erin E. [1 ,2 ,3 ,4 ]
机构
[1] Univ Minnesota, Dept Chem, 207 Pleasant St SE, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Med Chem, 208 Harvard St SE, Minneapolis, MN 55454 USA
[3] Univ Minnesota, Dept Biochem Mol Biol & Biophys, 321 Church St SE, Minneapolis, MN 55454 USA
[4] Univ Minnesota, Dept Pharmacol, 321 Church St SE, Minneapolis, MN 55454 USA
关键词
IV PILI; IDENTIFICATION; ANTIBIOTICS;
D O I
10.1016/j.cbpa.2025.102571
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
Bacterial infections, especially those that are resistant to antibiotics, constitute an increasing threat to public health. Deeper understanding about the systems that govern resistant infections, followed by the design of new therapies is crucial to minimizing morbidity and mortality due to antibacterial resistance. To this end, the discovery of small molecules capable of modulating bacterial processes is an important goal. Herein, we summarize recent developments in high-throughput screening, including the use of in vitro biochemical assays, reporter fusion read-out methods, and live cell phenotypic assays in bacteria. We also highlight key advantages and disadvantages of each assay type, as well as exciting new innovations.
引用
收藏
页数:11
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