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A unified mechanism for proteolysis and autocatalytic activation in the 20S proteasome

Biogenesis of the 20S proteasome is tightly regulated. The N-terminal propeptides protecting the active-site threonines are autocatalytically released only on completion of assembly. However, the trigger for the self-activation and the reason for the strict conservation of threonine as the active si...

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Autores principales: Huber, Eva M., Heinemeyer, Wolfgang, Li, Xia, Arendt, Cassandra S., Hochstrasser, Mark, Groll, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4792962/
https://www.ncbi.nlm.nih.gov/pubmed/26964885
http://dx.doi.org/10.1038/ncomms10900
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author Huber, Eva M.
Heinemeyer, Wolfgang
Li, Xia
Arendt, Cassandra S.
Hochstrasser, Mark
Groll, Michael
author_facet Huber, Eva M.
Heinemeyer, Wolfgang
Li, Xia
Arendt, Cassandra S.
Hochstrasser, Mark
Groll, Michael
author_sort Huber, Eva M.
collection PubMed
description Biogenesis of the 20S proteasome is tightly regulated. The N-terminal propeptides protecting the active-site threonines are autocatalytically released only on completion of assembly. However, the trigger for the self-activation and the reason for the strict conservation of threonine as the active site nucleophile remain enigmatic. Here we use mutagenesis, X-ray crystallography and biochemical assays to suggest that Lys33 initiates nucleophilic attack of the propeptide by deprotonating the Thr1 hydroxyl group and that both residues together with Asp17 are part of a catalytic triad. Substitution of Thr1 by Cys disrupts the interaction with Lys33 and inactivates the proteasome. Although a Thr1Ser mutant is active, it is less efficient compared with wild type because of the unfavourable orientation of Ser1 towards incoming substrates. This work provides insights into the basic mechanism of proteolysis and propeptide autolysis, as well as the evolutionary pressures that drove the proteasome to become a threonine protease.
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spelling pubmed-47929622016-03-21 A unified mechanism for proteolysis and autocatalytic activation in the 20S proteasome Huber, Eva M. Heinemeyer, Wolfgang Li, Xia Arendt, Cassandra S. Hochstrasser, Mark Groll, Michael Nat Commun Article Biogenesis of the 20S proteasome is tightly regulated. The N-terminal propeptides protecting the active-site threonines are autocatalytically released only on completion of assembly. However, the trigger for the self-activation and the reason for the strict conservation of threonine as the active site nucleophile remain enigmatic. Here we use mutagenesis, X-ray crystallography and biochemical assays to suggest that Lys33 initiates nucleophilic attack of the propeptide by deprotonating the Thr1 hydroxyl group and that both residues together with Asp17 are part of a catalytic triad. Substitution of Thr1 by Cys disrupts the interaction with Lys33 and inactivates the proteasome. Although a Thr1Ser mutant is active, it is less efficient compared with wild type because of the unfavourable orientation of Ser1 towards incoming substrates. This work provides insights into the basic mechanism of proteolysis and propeptide autolysis, as well as the evolutionary pressures that drove the proteasome to become a threonine protease. Nature Publishing Group 2016-03-11 /pmc/articles/PMC4792962/ /pubmed/26964885 http://dx.doi.org/10.1038/ncomms10900 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Huber, Eva M.
Heinemeyer, Wolfgang
Li, Xia
Arendt, Cassandra S.
Hochstrasser, Mark
Groll, Michael
A unified mechanism for proteolysis and autocatalytic activation in the 20S proteasome
title A unified mechanism for proteolysis and autocatalytic activation in the 20S proteasome
title_full A unified mechanism for proteolysis and autocatalytic activation in the 20S proteasome
title_fullStr A unified mechanism for proteolysis and autocatalytic activation in the 20S proteasome
title_full_unstemmed A unified mechanism for proteolysis and autocatalytic activation in the 20S proteasome
title_short A unified mechanism for proteolysis and autocatalytic activation in the 20S proteasome
title_sort unified mechanism for proteolysis and autocatalytic activation in the 20s proteasome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4792962/
https://www.ncbi.nlm.nih.gov/pubmed/26964885
http://dx.doi.org/10.1038/ncomms10900
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