Chemical Biology of Sortase A Inhibition: A Gateway to Anti-infective Therapeutic Agents
Overview
Affiliations
is the leading cause of hospital-acquired infections. The enzyme sortase A, present on the cell surface of , plays a key role in bacterial virulence without affecting the bacterial viability. Inhibition of sortase A activity offers a powerful but clinically less explored therapeutic strategy, as it offers the possibility of not inducing any selective pressure on the bacteria to evolve drug-resistant strains. In this Perspective, we offer a chemical space narrative for the design of sortase A inhibitors, as delineated into three broad domains: peptidomimetics, natural products, and synthetic small molecules. This provides immense opportunities for medicinal chemists to alleviate the ever-growing crisis of antibiotic resistance.
Ensemble Docking as a Tool for the Rational Design of Peptidomimetic Sortase A Inhibitors.
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PMID: 39457061 PMC: 11508331. DOI: 10.3390/ijms252011279.
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PMID: 38921577 PMC: 11204543. DOI: 10.3390/md22060266.
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PMID: 37623712 PMC: 10455474. DOI: 10.3390/md21080431.
The enzyme activity of sortase A is regulated by phosphorylation in .
Chen F, Di H, Wang Y, Peng C, Chen R, Pan H Virulence. 2023; 14(1):2171641.
PMID: 36694285 PMC: 9928477. DOI: 10.1080/21505594.2023.2171641.
Oligopeptide Sortase Inhibitor Modulates Cell Adhesion and Biofilm Formation.
Bozhkova S, Gordina E, Labutin D, Kudryavtsev K Antibiotics (Basel). 2022; 11(12).
PMID: 36551492 PMC: 9774600. DOI: 10.3390/antibiotics11121836.