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On the Mechanism of Action of SJ-172550 in Inhibiting the Interaction of MDM4 and p53
SJ-172550 (1) was previously discovered in a biochemical high throughput screen for inhibitors of the interaction of MDMX and p53 and characterized as a reversible inhibitor (J. Biol. Chem. 2010; 285∶10786). Further study of the biochemical mode of action of 1 has shown that it acts through a compli...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3366986/ https://www.ncbi.nlm.nih.gov/pubmed/22675482 http://dx.doi.org/10.1371/journal.pone.0037518 |
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author | Bista, Michal Smithson, David Pecak, Aleksandra Salinas, Gabriella Pustelny, Katarzyna Min, Jaeki Pirog, Artur Finch, Kristin Zdzalik, Michal Waddell, Brett Wladyka, Benedykt Kedracka-Krok, Sylwia Dyer, Michael A. Dubin, Grzegorz Guy, R. Kiplin |
author_facet | Bista, Michal Smithson, David Pecak, Aleksandra Salinas, Gabriella Pustelny, Katarzyna Min, Jaeki Pirog, Artur Finch, Kristin Zdzalik, Michal Waddell, Brett Wladyka, Benedykt Kedracka-Krok, Sylwia Dyer, Michael A. Dubin, Grzegorz Guy, R. Kiplin |
author_sort | Bista, Michal |
collection | PubMed |
description | SJ-172550 (1) was previously discovered in a biochemical high throughput screen for inhibitors of the interaction of MDMX and p53 and characterized as a reversible inhibitor (J. Biol. Chem. 2010; 285∶10786). Further study of the biochemical mode of action of 1 has shown that it acts through a complicated mechanism in which the compound forms a covalent but reversible complex with MDMX and locks MDMX into a conformation that is unable to bind p53. The relative stability of this complex is influenced by many factors including the reducing potential of the media, the presence of aggregates, and other factors that influence the conformational stability of the protein. This complex mechanism of action hinders the further development of compound 1 as a selective MDMX inhibitor. |
format | Online Article Text |
id | pubmed-3366986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33669862012-06-06 On the Mechanism of Action of SJ-172550 in Inhibiting the Interaction of MDM4 and p53 Bista, Michal Smithson, David Pecak, Aleksandra Salinas, Gabriella Pustelny, Katarzyna Min, Jaeki Pirog, Artur Finch, Kristin Zdzalik, Michal Waddell, Brett Wladyka, Benedykt Kedracka-Krok, Sylwia Dyer, Michael A. Dubin, Grzegorz Guy, R. Kiplin PLoS One Research Article SJ-172550 (1) was previously discovered in a biochemical high throughput screen for inhibitors of the interaction of MDMX and p53 and characterized as a reversible inhibitor (J. Biol. Chem. 2010; 285∶10786). Further study of the biochemical mode of action of 1 has shown that it acts through a complicated mechanism in which the compound forms a covalent but reversible complex with MDMX and locks MDMX into a conformation that is unable to bind p53. The relative stability of this complex is influenced by many factors including the reducing potential of the media, the presence of aggregates, and other factors that influence the conformational stability of the protein. This complex mechanism of action hinders the further development of compound 1 as a selective MDMX inhibitor. Public Library of Science 2012-06-04 /pmc/articles/PMC3366986/ /pubmed/22675482 http://dx.doi.org/10.1371/journal.pone.0037518 Text en Bista 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 Bista, Michal Smithson, David Pecak, Aleksandra Salinas, Gabriella Pustelny, Katarzyna Min, Jaeki Pirog, Artur Finch, Kristin Zdzalik, Michal Waddell, Brett Wladyka, Benedykt Kedracka-Krok, Sylwia Dyer, Michael A. Dubin, Grzegorz Guy, R. Kiplin On the Mechanism of Action of SJ-172550 in Inhibiting the Interaction of MDM4 and p53 |
title | On the Mechanism of Action of SJ-172550 in Inhibiting the Interaction of MDM4 and p53 |
title_full | On the Mechanism of Action of SJ-172550 in Inhibiting the Interaction of MDM4 and p53 |
title_fullStr | On the Mechanism of Action of SJ-172550 in Inhibiting the Interaction of MDM4 and p53 |
title_full_unstemmed | On the Mechanism of Action of SJ-172550 in Inhibiting the Interaction of MDM4 and p53 |
title_short | On the Mechanism of Action of SJ-172550 in Inhibiting the Interaction of MDM4 and p53 |
title_sort | on the mechanism of action of sj-172550 in inhibiting the interaction of mdm4 and p53 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3366986/ https://www.ncbi.nlm.nih.gov/pubmed/22675482 http://dx.doi.org/10.1371/journal.pone.0037518 |
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