| Literature DB >> 36268122 |
Camilla Ruffilli1,2, Sascha Roth1, Monica Rodrigo1, Helen Boyd3, Noam Zelcer2, Kevin Moreau1.
Abstract
Targeted protein degradation (TPD) is a promising therapeutic modality to modulate protein levels and its application promises to reduce the "undruggable" proteome. Among TPD strategies, Proteolysis TArgeting Chimera (PROTAC) technology has shown a tremendous potential with attractive advantages when compared to the inhibition of the same target. While PROTAC technology has had a significant impact in scientific research, its application to degrade integral membrane proteins (IMPs) is still in its beginnings. Among the 15 compounds having entered clinical trials by the end of 2021, only two targets are membrane-associated proteins. In this review we are discussing the potential reasons which may underlie this, and we are presenting new tools that have been recently developed to solve these limitations and to empower the use of PROTACs to target IMPs.Entities:
Year: 2022 PMID: 36268122 PMCID: PMC9578132 DOI: 10.1021/acsptsci.2c00142
Source DB: PubMed Journal: ACS Pharmacol Transl Sci ISSN: 2575-9108