The Complete Assessment of Small Molecule and Peptidomimetic Inhibitors of Sortase A Towards Antivirulence Treatment.
Jordi C J HintzenHelal AbujubaraAlesia A TietzeAlesia A TietzePublished in: Chemistry (Weinheim an der Bergstrasse, Germany) (2024)
This review covers the most recent advances in the development of inhibitors for the bacterial enzyme sortase A (SrtA). Sortase A (SrtA) is a critical virulence factor, present ubiquitously in Gram-positive bacteria of which many are pathogenic. Sortases are key enzymes regulating bacterial adherence to host cells, by anchoring extracellular matrix-binding proteins to the bacterial outer cell wall. By targeting virulence factors, effective treatment can be achieved, without inducing antibiotic resistance to the treatment. This is a potentially more sustainable, long-term approach to treating bacterial infections, including ones that display multiple resistance to current therapeutics. There are many promising approaches available for SrtA inhibition, some of which have the potential to advance into further clinical development, with peptidomimetic and in vivo active small molecules being among the most promising. There are currently no approved drugs on the market targeting SrtA, despite its promise, adding to the relevance of this review article, as it extends to the pharmaceutical industry additionally to academic researchers.
Keyphrases
- small molecule
- extracellular matrix
- escherichia coli
- pseudomonas aeruginosa
- staphylococcus aureus
- cell wall
- induced apoptosis
- type diabetes
- machine learning
- multidrug resistant
- antimicrobial resistance
- cell proliferation
- oxidative stress
- biofilm formation
- cancer therapy
- gram negative
- drug delivery
- risk assessment
- big data
- artificial intelligence
- medical students
- cell cycle arrest