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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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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. |
format | Online Article Text |
id | pubmed-4792962 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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