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Sialic Acid Derivatives Inhibit SiaT Transporters and Delay Bacterial Growth

[Image: see text] Antibiotic resistance is a major worldwide concern, and new drugs with mechanistically novel modes of action are urgently needed. Here, we report the structure-based drug design, synthesis, and evaluation in vitro and in cellular systems of sialic acid derivatives able to inhibit t...

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Detalles Bibliográficos
Autores principales: Bozzola, Tiago, Scalise, Mariafrancesca, Larsson, Christer U., Newton-Vesty, Michael C., Rovegno, Caterina, Mitra, Ankita, Cramer, Jonathan, Wahlgren, Weixiao Yuan, Radhakrishnan Santhakumari, Partha, Johnsson, Richard E., Schwardt, Oliver, Ernst, Beat, Friemann, Rosmarie, Dobson, Renwick C. J., Indiveri, Cesare, Schelin, Jenny, Nilsson, Ulf J., Ellervik, Ulf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9295122/
https://www.ncbi.nlm.nih.gov/pubmed/35675124
http://dx.doi.org/10.1021/acschembio.2c00321
Descripción
Sumario:[Image: see text] Antibiotic resistance is a major worldwide concern, and new drugs with mechanistically novel modes of action are urgently needed. Here, we report the structure-based drug design, synthesis, and evaluation in vitro and in cellular systems of sialic acid derivatives able to inhibit the bacterial sialic acid symporter SiaT. We designed and synthesized 21 sialic acid derivatives and screened their affinity for SiaT by a thermal shift assay and elucidated the inhibitory mechanism through binding thermodynamics, computational methods, and inhibitory kinetic studies. The most potent compounds, which have a 180-fold higher affinity compared to the natural substrate, were tested in bacterial growth assays and indicate bacterial growth delay in methicillin-resistant Staphylococcus aureus. This study represents the first example and a promising lead in developing sialic acid uptake inhibitors as novel antibacterial agents.