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Cryo-EM as a powerful tool for drug discovery

The recent revolution in cryo-EM has produced an explosion of structures at near-atomic or better resolution. This has allowed cryo-EM structures to provide visualization of bound small-molecule ligands in the macromolecules, and these new structures have provided unprecedented insights into the mol...

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Autores principales: Van Drie, John H, Tong, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7467112/
https://www.ncbi.nlm.nih.gov/pubmed/32890683
http://dx.doi.org/10.1016/j.bmcl.2020.127524
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author Van Drie, John H
Tong, Liang
author_facet Van Drie, John H
Tong, Liang
author_sort Van Drie, John H
collection PubMed
description The recent revolution in cryo-EM has produced an explosion of structures at near-atomic or better resolution. This has allowed cryo-EM structures to provide visualization of bound small-molecule ligands in the macromolecules, and these new structures have provided unprecedented insights into the molecular mechanisms of complex biochemical processes. They have also had a profound impact on drug discovery, defining the binding modes and mechanisms of action of well-known drugs as well as driving the design and development of new compounds. This review will summarize and highlight some of these structures. Most excitingly, the latest cryo-EM technology has produced structures at 1.2 Å resolution, further solidifying cryo-EM as a powerful tool for drug discovery. Therefore, cryo-EM will play an ever-increasing role in drug discovery in the coming years.
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spelling pubmed-74671122020-09-03 Cryo-EM as a powerful tool for drug discovery Van Drie, John H Tong, Liang Bioorg Med Chem Lett Digest The recent revolution in cryo-EM has produced an explosion of structures at near-atomic or better resolution. This has allowed cryo-EM structures to provide visualization of bound small-molecule ligands in the macromolecules, and these new structures have provided unprecedented insights into the molecular mechanisms of complex biochemical processes. They have also had a profound impact on drug discovery, defining the binding modes and mechanisms of action of well-known drugs as well as driving the design and development of new compounds. This review will summarize and highlight some of these structures. Most excitingly, the latest cryo-EM technology has produced structures at 1.2 Å resolution, further solidifying cryo-EM as a powerful tool for drug discovery. Therefore, cryo-EM will play an ever-increasing role in drug discovery in the coming years. Elsevier Ltd. 2020-11-15 2020-09-02 /pmc/articles/PMC7467112/ /pubmed/32890683 http://dx.doi.org/10.1016/j.bmcl.2020.127524 Text en © 2020 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Digest
Van Drie, John H
Tong, Liang
Cryo-EM as a powerful tool for drug discovery
title Cryo-EM as a powerful tool for drug discovery
title_full Cryo-EM as a powerful tool for drug discovery
title_fullStr Cryo-EM as a powerful tool for drug discovery
title_full_unstemmed Cryo-EM as a powerful tool for drug discovery
title_short Cryo-EM as a powerful tool for drug discovery
title_sort cryo-em as a powerful tool for drug discovery
topic Digest
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7467112/
https://www.ncbi.nlm.nih.gov/pubmed/32890683
http://dx.doi.org/10.1016/j.bmcl.2020.127524
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