Proteolysis-targeting chimera (PROTAC) delivery system: advancing protein degraders towards clinical translation. (17th June 2022)
- Record Type:
- Journal Article
- Title:
- Proteolysis-targeting chimera (PROTAC) delivery system: advancing protein degraders towards clinical translation. (17th June 2022)
- Main Title:
- Proteolysis-targeting chimera (PROTAC) delivery system: advancing protein degraders towards clinical translation
- Authors:
- Chen, Yu
Tandon, Ira
Heelan, William
Wang, Yixin
Tang, Weiping
Hu, Quanyin - Abstract:
- Abstract : This tutorial review discusses the convergence of drug delivery systems and PROTACs, surveys the burgeoning PROTAC delivery strategies, summarizes their design principles, clarifies their challenges, and outlooks future translational opportunities. Abstract : Proteolysis Targeting Chimeras (PROTACs), an emerging therapeutic entity designed to degrade target proteins by hijacking the ubiquitin–proteasome system, have the potential to revolutionize the healthcare industry. The broad applicability of this protein degradation strategy has been verified with a few E3 ligases and a variety of distinct targets through the construction of modular chimeric structures. Despite recent efforts to promote the use of PROTACs for clinical applications, most PROTACs do not make it beyond the preclinical stage of drug development. There are several reasons that prevent PROTACs from reaching the market, and the inadequate delivery to the target site is one of the most challenging hurdles. With the increasing need for accelerating the translational process, combining the concepts of PROTACs and delivery systems has been explored to enhance the in vivo performance of PROTACs. These improved delivery strategies can eliminate unfavorable physicochemical properties of PROTACs, improve their targetability, and decrease their off-target side effects. The integration of powerful PROTACs and versatile delivery systems will inaugurate a burgeoning orientation for the field of targetedAbstract : This tutorial review discusses the convergence of drug delivery systems and PROTACs, surveys the burgeoning PROTAC delivery strategies, summarizes their design principles, clarifies their challenges, and outlooks future translational opportunities. Abstract : Proteolysis Targeting Chimeras (PROTACs), an emerging therapeutic entity designed to degrade target proteins by hijacking the ubiquitin–proteasome system, have the potential to revolutionize the healthcare industry. The broad applicability of this protein degradation strategy has been verified with a few E3 ligases and a variety of distinct targets through the construction of modular chimeric structures. Despite recent efforts to promote the use of PROTACs for clinical applications, most PROTACs do not make it beyond the preclinical stage of drug development. There are several reasons that prevent PROTACs from reaching the market, and the inadequate delivery to the target site is one of the most challenging hurdles. With the increasing need for accelerating the translational process, combining the concepts of PROTACs and delivery systems has been explored to enhance the in vivo performance of PROTACs. These improved delivery strategies can eliminate unfavorable physicochemical properties of PROTACs, improve their targetability, and decrease their off-target side effects. The integration of powerful PROTACs and versatile delivery systems will inaugurate a burgeoning orientation for the field of targeted protein degradation. In this review, we will survey the latest progress in improving the in vivo degradation efficacy of PROTACs through delivery strategies, outline design principles for PROTAC-based delivery systems, discuss the current challenges with PROTACs, and outlook future opportunities in this field. … (more)
- Is Part Of:
- Chemical Society reviews. Volume 51:Number 13(2022)
- Journal:
- Chemical Society reviews
- Issue:
- Volume 51:Number 13(2022)
- Issue Display:
- Volume 51, Issue 13 (2022)
- Year:
- 2022
- Volume:
- 51
- Issue:
- 13
- Issue Sort Value:
- 2022-0051-0013-0000
- Page Start:
- 5330
- Page End:
- 5350
- Publication Date:
- 2022-06-17
- Subjects:
- Chemistry -- Periodicals
540 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cs#!recentarticles&adv ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d1cs00762a ↗
- Languages:
- English
- ISSNs:
- 0306-0012
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3151.550000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 22272.xml