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The Contribution of the 20S Proteasome to Proteostasis
The last decade has seen accumulating evidence of various proteins being degraded by the core 20S proteasome, without its regulatory particle(s). Here, we will describe recent advances in our knowledge of the functional aspects of the 20S proteasome, exploring several different systems and processes...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6571867/ https://www.ncbi.nlm.nih.gov/pubmed/31100951 http://dx.doi.org/10.3390/biom9050190 |
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author | Kumar Deshmukh, Fanindra Yaffe, Dana Olshina, Maya A. Ben-Nissan, Gili Sharon, Michal |
author_facet | Kumar Deshmukh, Fanindra Yaffe, Dana Olshina, Maya A. Ben-Nissan, Gili Sharon, Michal |
author_sort | Kumar Deshmukh, Fanindra |
collection | PubMed |
description | The last decade has seen accumulating evidence of various proteins being degraded by the core 20S proteasome, without its regulatory particle(s). Here, we will describe recent advances in our knowledge of the functional aspects of the 20S proteasome, exploring several different systems and processes. These include neuronal communication, post-translational processing, oxidative stress, intrinsically disordered protein regulation, and extracellular proteasomes. Taken together, these findings suggest that the 20S proteasome, like the well-studied 26S proteasome, is involved in multiple biological processes. Clarifying our understanding of its workings calls for a transformation in our perception of 20S proteasome-mediated degradation—no longer as a passive and marginal path, but rather as an independent, coordinated biological process. Nevertheless, in spite of impressive progress made thus far, the field still lags far behind the front lines of 26S proteasome research. Therefore, we also touch on the gaps in our knowledge of the 20S proteasome that remain to be bridged in the future. |
format | Online Article Text |
id | pubmed-6571867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-65718672019-06-18 The Contribution of the 20S Proteasome to Proteostasis Kumar Deshmukh, Fanindra Yaffe, Dana Olshina, Maya A. Ben-Nissan, Gili Sharon, Michal Biomolecules Review The last decade has seen accumulating evidence of various proteins being degraded by the core 20S proteasome, without its regulatory particle(s). Here, we will describe recent advances in our knowledge of the functional aspects of the 20S proteasome, exploring several different systems and processes. These include neuronal communication, post-translational processing, oxidative stress, intrinsically disordered protein regulation, and extracellular proteasomes. Taken together, these findings suggest that the 20S proteasome, like the well-studied 26S proteasome, is involved in multiple biological processes. Clarifying our understanding of its workings calls for a transformation in our perception of 20S proteasome-mediated degradation—no longer as a passive and marginal path, but rather as an independent, coordinated biological process. Nevertheless, in spite of impressive progress made thus far, the field still lags far behind the front lines of 26S proteasome research. Therefore, we also touch on the gaps in our knowledge of the 20S proteasome that remain to be bridged in the future. MDPI 2019-05-16 /pmc/articles/PMC6571867/ /pubmed/31100951 http://dx.doi.org/10.3390/biom9050190 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Kumar Deshmukh, Fanindra Yaffe, Dana Olshina, Maya A. Ben-Nissan, Gili Sharon, Michal The Contribution of the 20S Proteasome to Proteostasis |
title | The Contribution of the 20S Proteasome to Proteostasis |
title_full | The Contribution of the 20S Proteasome to Proteostasis |
title_fullStr | The Contribution of the 20S Proteasome to Proteostasis |
title_full_unstemmed | The Contribution of the 20S Proteasome to Proteostasis |
title_short | The Contribution of the 20S Proteasome to Proteostasis |
title_sort | contribution of the 20s proteasome to proteostasis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6571867/ https://www.ncbi.nlm.nih.gov/pubmed/31100951 http://dx.doi.org/10.3390/biom9050190 |
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