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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...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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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. |
format | Online Article Text |
id | pubmed-9295122 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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