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Development of inhibitors in the ubiquitination cascade
The ubiquitin proteasome system (UPS) is essential in regulating myriad aspects of protein functions. It is therefore a fundamentally important regulatory mechanism that impacts most if not all aspects of cellular processes. Indeed, malfunction of UPS components is implicated in human diseases such...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094371/ https://www.ncbi.nlm.nih.gov/pubmed/24239534 http://dx.doi.org/10.1016/j.febslet.2013.11.003 |
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author | Zhang, Wei Sidhu, Sachdev S. |
author_facet | Zhang, Wei Sidhu, Sachdev S. |
author_sort | Zhang, Wei |
collection | PubMed |
description | The ubiquitin proteasome system (UPS) is essential in regulating myriad aspects of protein functions. It is therefore a fundamentally important regulatory mechanism that impacts most if not all aspects of cellular processes. Indeed, malfunction of UPS components is implicated in human diseases such as neurodegenerative and immunological disorders and many cancers. The success of proteasome inhibitors in cancer therapy suggests that modulating enzymes in the ubiquitination cascade would be clinically important for therapeutic benefits. In this review, we summarize advances in developing inhibitors of a variety of UPS components. In particular, we highlight recent work done on the protein engineering of ubiquitin as modulators of the UPS, a novel approach that may shed light on innovative drug discovery in the future. |
format | Online Article Text |
id | pubmed-7094371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70943712020-03-25 Development of inhibitors in the ubiquitination cascade Zhang, Wei Sidhu, Sachdev S. FEBS Lett Review Articles The ubiquitin proteasome system (UPS) is essential in regulating myriad aspects of protein functions. It is therefore a fundamentally important regulatory mechanism that impacts most if not all aspects of cellular processes. Indeed, malfunction of UPS components is implicated in human diseases such as neurodegenerative and immunological disorders and many cancers. The success of proteasome inhibitors in cancer therapy suggests that modulating enzymes in the ubiquitination cascade would be clinically important for therapeutic benefits. In this review, we summarize advances in developing inhibitors of a variety of UPS components. In particular, we highlight recent work done on the protein engineering of ubiquitin as modulators of the UPS, a novel approach that may shed light on innovative drug discovery in the future. John Wiley and Sons Inc. 2014-01-21 2013-11-12 /pmc/articles/PMC7094371/ /pubmed/24239534 http://dx.doi.org/10.1016/j.febslet.2013.11.003 Text en FEBS Letters 588 (2014) 1873-3468 © 2015 Federation of European Biochemical Societies This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency. |
spellingShingle | Review Articles Zhang, Wei Sidhu, Sachdev S. Development of inhibitors in the ubiquitination cascade |
title | Development of inhibitors in the ubiquitination cascade |
title_full | Development of inhibitors in the ubiquitination cascade |
title_fullStr | Development of inhibitors in the ubiquitination cascade |
title_full_unstemmed | Development of inhibitors in the ubiquitination cascade |
title_short | Development of inhibitors in the ubiquitination cascade |
title_sort | development of inhibitors in the ubiquitination cascade |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094371/ https://www.ncbi.nlm.nih.gov/pubmed/24239534 http://dx.doi.org/10.1016/j.febslet.2013.11.003 |
work_keys_str_mv | AT zhangwei developmentofinhibitorsintheubiquitinationcascade AT sidhusachdevs developmentofinhibitorsintheubiquitinationcascade |