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Targeting Ribonucleases with Small Molecules and Bifunctional Molecules
[Image: see text] Ribonucleases (RNases) cleave and process RNAs, thereby regulating the biogenesis, metabolism, and degradation of coding and noncoding RNAs. Thus, small molecules targeting RNases have the potential to perturb RNA biology, and RNases have been studied as therapeutic targets of anti...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10594538/ https://www.ncbi.nlm.nih.gov/pubmed/37382390 http://dx.doi.org/10.1021/acschembio.3c00191 |
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author | Borgelt, Lydia Wu, Peng |
author_facet | Borgelt, Lydia Wu, Peng |
author_sort | Borgelt, Lydia |
collection | PubMed |
description | [Image: see text] Ribonucleases (RNases) cleave and process RNAs, thereby regulating the biogenesis, metabolism, and degradation of coding and noncoding RNAs. Thus, small molecules targeting RNases have the potential to perturb RNA biology, and RNases have been studied as therapeutic targets of antibiotics, antivirals, and agents for autoimmune diseases and cancers. Additionally, the recent advances in chemically induced proximity approaches have led to the discovery of bifunctional molecules that target RNases to achieve RNA degradation or inhibit RNA processing. Here, we summarize the efforts that have been made to discover small-molecule inhibitors and activators targeting bacterial, viral, and human RNases. We also highlight the emerging examples of RNase-targeting bifunctional molecules and discuss the trends in developing such molecules for both biological and therapeutic applications. |
format | Online Article Text |
id | pubmed-10594538 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-105945382023-10-25 Targeting Ribonucleases with Small Molecules and Bifunctional Molecules Borgelt, Lydia Wu, Peng ACS Chem Biol [Image: see text] Ribonucleases (RNases) cleave and process RNAs, thereby regulating the biogenesis, metabolism, and degradation of coding and noncoding RNAs. Thus, small molecules targeting RNases have the potential to perturb RNA biology, and RNases have been studied as therapeutic targets of antibiotics, antivirals, and agents for autoimmune diseases and cancers. Additionally, the recent advances in chemically induced proximity approaches have led to the discovery of bifunctional molecules that target RNases to achieve RNA degradation or inhibit RNA processing. Here, we summarize the efforts that have been made to discover small-molecule inhibitors and activators targeting bacterial, viral, and human RNases. We also highlight the emerging examples of RNase-targeting bifunctional molecules and discuss the trends in developing such molecules for both biological and therapeutic applications. American Chemical Society 2023-06-29 /pmc/articles/PMC10594538/ /pubmed/37382390 http://dx.doi.org/10.1021/acschembio.3c00191 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Borgelt, Lydia Wu, Peng Targeting Ribonucleases with Small Molecules and Bifunctional Molecules |
title | Targeting Ribonucleases with Small Molecules and Bifunctional
Molecules |
title_full | Targeting Ribonucleases with Small Molecules and Bifunctional
Molecules |
title_fullStr | Targeting Ribonucleases with Small Molecules and Bifunctional
Molecules |
title_full_unstemmed | Targeting Ribonucleases with Small Molecules and Bifunctional
Molecules |
title_short | Targeting Ribonucleases with Small Molecules and Bifunctional
Molecules |
title_sort | targeting ribonucleases with small molecules and bifunctional
molecules |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10594538/ https://www.ncbi.nlm.nih.gov/pubmed/37382390 http://dx.doi.org/10.1021/acschembio.3c00191 |
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