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Discovery of Novel MDR-Mycobacterium tuberculosis Inhibitor by New FRIGATE Computational Screen

With 1.6 million casualties annually and 2 billion people being infected, tuberculosis is still one of the most pressing healthcare challenges. Here we report on the new computational docking algorithm FRIGATE which unites continuous local optimization techniques (conjugate gradient method) with an...

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Detalles Bibliográficos
Autores principales: Scheich, Christoph, Szabadka, Zoltán, Vértessy, Beáta, Pütter, Vera, Grolmusz, Vince, Schade, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3229595/
https://www.ncbi.nlm.nih.gov/pubmed/22164290
http://dx.doi.org/10.1371/journal.pone.0028428
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author Scheich, Christoph
Szabadka, Zoltán
Vértessy, Beáta
Pütter, Vera
Grolmusz, Vince
Schade, Markus
author_facet Scheich, Christoph
Szabadka, Zoltán
Vértessy, Beáta
Pütter, Vera
Grolmusz, Vince
Schade, Markus
author_sort Scheich, Christoph
collection PubMed
description With 1.6 million casualties annually and 2 billion people being infected, tuberculosis is still one of the most pressing healthcare challenges. Here we report on the new computational docking algorithm FRIGATE which unites continuous local optimization techniques (conjugate gradient method) with an inherently discrete computational approach in forcefield computation, resulting in equal or better scoring accuracies than several benchmark docking programs. By utilizing FRIGATE for a virtual screen of the ZINC library against the Mycobacterium tuberculosis (Mtb) enzyme antigen 85C, we identified novel small molecule inhibitors of multiple drug-resistant Mtb, which bind in vitro to the catalytic site of antigen 85C.
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spelling pubmed-32295952011-12-07 Discovery of Novel MDR-Mycobacterium tuberculosis Inhibitor by New FRIGATE Computational Screen Scheich, Christoph Szabadka, Zoltán Vértessy, Beáta Pütter, Vera Grolmusz, Vince Schade, Markus PLoS One Research Article With 1.6 million casualties annually and 2 billion people being infected, tuberculosis is still one of the most pressing healthcare challenges. Here we report on the new computational docking algorithm FRIGATE which unites continuous local optimization techniques (conjugate gradient method) with an inherently discrete computational approach in forcefield computation, resulting in equal or better scoring accuracies than several benchmark docking programs. By utilizing FRIGATE for a virtual screen of the ZINC library against the Mycobacterium tuberculosis (Mtb) enzyme antigen 85C, we identified novel small molecule inhibitors of multiple drug-resistant Mtb, which bind in vitro to the catalytic site of antigen 85C. Public Library of Science 2011-12-02 /pmc/articles/PMC3229595/ /pubmed/22164290 http://dx.doi.org/10.1371/journal.pone.0028428 Text en Scheich et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Scheich, Christoph
Szabadka, Zoltán
Vértessy, Beáta
Pütter, Vera
Grolmusz, Vince
Schade, Markus
Discovery of Novel MDR-Mycobacterium tuberculosis Inhibitor by New FRIGATE Computational Screen
title Discovery of Novel MDR-Mycobacterium tuberculosis Inhibitor by New FRIGATE Computational Screen
title_full Discovery of Novel MDR-Mycobacterium tuberculosis Inhibitor by New FRIGATE Computational Screen
title_fullStr Discovery of Novel MDR-Mycobacterium tuberculosis Inhibitor by New FRIGATE Computational Screen
title_full_unstemmed Discovery of Novel MDR-Mycobacterium tuberculosis Inhibitor by New FRIGATE Computational Screen
title_short Discovery of Novel MDR-Mycobacterium tuberculosis Inhibitor by New FRIGATE Computational Screen
title_sort discovery of novel mdr-mycobacterium tuberculosis inhibitor by new frigate computational screen
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3229595/
https://www.ncbi.nlm.nih.gov/pubmed/22164290
http://dx.doi.org/10.1371/journal.pone.0028428
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