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Opportunities and Challenges of Small Molecule Induced Targeted Protein Degradation

Proteolysis targeting chimeras (PROTAC) represents a new type of small molecule induced protein degradation technology that has emerged in recent years. PROTAC uses bifunctional small molecules to induce ubiquitination of target proteins and utilizes intracellular proteasomes for chemical knockdown....

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Detalles Bibliográficos
Autores principales: He, Ming, Lv, Wenxing, Rao, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8261656/
https://www.ncbi.nlm.nih.gov/pubmed/34249939
http://dx.doi.org/10.3389/fcell.2021.685106
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author He, Ming
Lv, Wenxing
Rao, Yu
author_facet He, Ming
Lv, Wenxing
Rao, Yu
author_sort He, Ming
collection PubMed
description Proteolysis targeting chimeras (PROTAC) represents a new type of small molecule induced protein degradation technology that has emerged in recent years. PROTAC uses bifunctional small molecules to induce ubiquitination of target proteins and utilizes intracellular proteasomes for chemical knockdown. It complements the gene editing and RNA interference for protein knockdown. Compared with small molecule inhibitors, PROTAC has shown great advantages in overcoming tumor resistance, affecting the non-enzymatic function of target proteins, degrading undruggable targets, and providing new rapid and reversible chemical knockout tools. At the same time, its challenges and problems also need to be resolved as a fast-developing newchemical biology technology.
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spelling pubmed-82616562021-07-08 Opportunities and Challenges of Small Molecule Induced Targeted Protein Degradation He, Ming Lv, Wenxing Rao, Yu Front Cell Dev Biol Cell and Developmental Biology Proteolysis targeting chimeras (PROTAC) represents a new type of small molecule induced protein degradation technology that has emerged in recent years. PROTAC uses bifunctional small molecules to induce ubiquitination of target proteins and utilizes intracellular proteasomes for chemical knockdown. It complements the gene editing and RNA interference for protein knockdown. Compared with small molecule inhibitors, PROTAC has shown great advantages in overcoming tumor resistance, affecting the non-enzymatic function of target proteins, degrading undruggable targets, and providing new rapid and reversible chemical knockout tools. At the same time, its challenges and problems also need to be resolved as a fast-developing newchemical biology technology. Frontiers Media S.A. 2021-06-22 /pmc/articles/PMC8261656/ /pubmed/34249939 http://dx.doi.org/10.3389/fcell.2021.685106 Text en Copyright © 2021 He, Lv and Rao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
He, Ming
Lv, Wenxing
Rao, Yu
Opportunities and Challenges of Small Molecule Induced Targeted Protein Degradation
title Opportunities and Challenges of Small Molecule Induced Targeted Protein Degradation
title_full Opportunities and Challenges of Small Molecule Induced Targeted Protein Degradation
title_fullStr Opportunities and Challenges of Small Molecule Induced Targeted Protein Degradation
title_full_unstemmed Opportunities and Challenges of Small Molecule Induced Targeted Protein Degradation
title_short Opportunities and Challenges of Small Molecule Induced Targeted Protein Degradation
title_sort opportunities and challenges of small molecule induced targeted protein degradation
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8261656/
https://www.ncbi.nlm.nih.gov/pubmed/34249939
http://dx.doi.org/10.3389/fcell.2021.685106
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