Cargando…

BioSAXS–an emerging method to accelerate, enrich and de-risk antimicrobial drug development

Antimicrobial resistance is a worldwide threat to modern health care. Low-profit margin and high risk of cross-resistance resulted in a loss of interest in big pharma, contributing to the increasing threat. Strategies to address the problem are starting to emerge. Novel antimicrobial compounds with...

Descripción completa

Detalles Bibliográficos
Autores principales: Rumancev, Christoph, Rosenhahn, Axel, Hilpert, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9445215/
https://www.ncbi.nlm.nih.gov/pubmed/36081947
http://dx.doi.org/10.3389/fphar.2022.947005
_version_ 1784783379184484352
author Rumancev, Christoph
Rosenhahn, Axel
Hilpert, Kai
author_facet Rumancev, Christoph
Rosenhahn, Axel
Hilpert, Kai
author_sort Rumancev, Christoph
collection PubMed
description Antimicrobial resistance is a worldwide threat to modern health care. Low-profit margin and high risk of cross-resistance resulted in a loss of interest in big pharma, contributing to the increasing threat. Strategies to address the problem are starting to emerge. Novel antimicrobial compounds with novel modes of action are especially valued because they have a lower risk of cross-resistance. Up to now determining the mode of action has been very time and resource consuming and will be performed once drug candidates were already progressed in preclinical development. BioSAXS is emerging as a new method to test up to thousands of compounds to classify them into groups based on ultra-structural changes that correlate to their modes of action. First experiments in E. coli (gram-negative) have demonstrated that using conventional and experimental antimicrobials a classification of compounds according to their mode of action was possible. Results were backed up by transmission electron microscopy. Further work showed that also gram-positive bacteria (Staphylococcus aureus) can be used and the effects of novel antimicrobial peptides on both types of bacteria were studied. Preliminary experiments also show that BioSAXS can be used to classify antifungal drugs, demonstrated on Candida albicans. In summary, BioSAXS can accelerate and enrich the discovery of antimicrobial compounds from screening projects with a novel mode of action and hence de-risk the development of urgently needed antimicrobial drugs.
format Online
Article
Text
id pubmed-9445215
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-94452152022-09-07 BioSAXS–an emerging method to accelerate, enrich and de-risk antimicrobial drug development Rumancev, Christoph Rosenhahn, Axel Hilpert, Kai Front Pharmacol Pharmacology Antimicrobial resistance is a worldwide threat to modern health care. Low-profit margin and high risk of cross-resistance resulted in a loss of interest in big pharma, contributing to the increasing threat. Strategies to address the problem are starting to emerge. Novel antimicrobial compounds with novel modes of action are especially valued because they have a lower risk of cross-resistance. Up to now determining the mode of action has been very time and resource consuming and will be performed once drug candidates were already progressed in preclinical development. BioSAXS is emerging as a new method to test up to thousands of compounds to classify them into groups based on ultra-structural changes that correlate to their modes of action. First experiments in E. coli (gram-negative) have demonstrated that using conventional and experimental antimicrobials a classification of compounds according to their mode of action was possible. Results were backed up by transmission electron microscopy. Further work showed that also gram-positive bacteria (Staphylococcus aureus) can be used and the effects of novel antimicrobial peptides on both types of bacteria were studied. Preliminary experiments also show that BioSAXS can be used to classify antifungal drugs, demonstrated on Candida albicans. In summary, BioSAXS can accelerate and enrich the discovery of antimicrobial compounds from screening projects with a novel mode of action and hence de-risk the development of urgently needed antimicrobial drugs. Frontiers Media S.A. 2022-08-23 /pmc/articles/PMC9445215/ /pubmed/36081947 http://dx.doi.org/10.3389/fphar.2022.947005 Text en Copyright © 2022 Rumancev, Rosenhahn and Hilpert. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Rumancev, Christoph
Rosenhahn, Axel
Hilpert, Kai
BioSAXS–an emerging method to accelerate, enrich and de-risk antimicrobial drug development
title BioSAXS–an emerging method to accelerate, enrich and de-risk antimicrobial drug development
title_full BioSAXS–an emerging method to accelerate, enrich and de-risk antimicrobial drug development
title_fullStr BioSAXS–an emerging method to accelerate, enrich and de-risk antimicrobial drug development
title_full_unstemmed BioSAXS–an emerging method to accelerate, enrich and de-risk antimicrobial drug development
title_short BioSAXS–an emerging method to accelerate, enrich and de-risk antimicrobial drug development
title_sort biosaxs–an emerging method to accelerate, enrich and de-risk antimicrobial drug development
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9445215/
https://www.ncbi.nlm.nih.gov/pubmed/36081947
http://dx.doi.org/10.3389/fphar.2022.947005
work_keys_str_mv AT rumancevchristoph biosaxsanemergingmethodtoaccelerateenrichandderiskantimicrobialdrugdevelopment
AT rosenhahnaxel biosaxsanemergingmethodtoaccelerateenrichandderiskantimicrobialdrugdevelopment
AT hilpertkai biosaxsanemergingmethodtoaccelerateenrichandderiskantimicrobialdrugdevelopment