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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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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
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author 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
author_facet 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
author_sort Bozzola, Tiago
collection PubMed
description [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.
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spelling pubmed-92951222022-07-20 Sialic Acid Derivatives Inhibit SiaT Transporters and Delay Bacterial Growth 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 ACS Chem Biol [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. American Chemical Society 2022-06-08 2022-07-15 /pmc/articles/PMC9295122/ /pubmed/35675124 http://dx.doi.org/10.1021/acschembio.2c00321 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle 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
Sialic Acid Derivatives Inhibit SiaT Transporters and Delay Bacterial Growth
title Sialic Acid Derivatives Inhibit SiaT Transporters and Delay Bacterial Growth
title_full Sialic Acid Derivatives Inhibit SiaT Transporters and Delay Bacterial Growth
title_fullStr Sialic Acid Derivatives Inhibit SiaT Transporters and Delay Bacterial Growth
title_full_unstemmed Sialic Acid Derivatives Inhibit SiaT Transporters and Delay Bacterial Growth
title_short Sialic Acid Derivatives Inhibit SiaT Transporters and Delay Bacterial Growth
title_sort sialic acid derivatives inhibit siat transporters and delay bacterial growth
url 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
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