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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
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.
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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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