Opportunities and challenges of PROTAC in the treatment of protein-driven diseases

Targeted protein degradation (TPD) has transformed the landscape of drug discovery by exploiting the ubiquitin-proteasome system (UPS) to eliminate, rather than inhibit, pathogenic proteins. This paradigm shift enables access to a vast array of previously “undruggable” targets and offers new therapeutic opportunities across diverse diseases. Among the available approaches, proteolysis-targeting chimera (PROTAC) have rapidly advanced from concept to clinical evaluation. Here we highlight the unique advantages of PROTAC in disease treatment and target identification, and examine emerging solutions to address key challenges such as pharmacokinetics, E3 ligase diversity, and selectivity. Together, these advances define a new era of precision therapeutics based on the controlled elimination of disease drivers.

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Publication Details

Journal
Results in Chemistry
Published
2026-03-13
DOI
https://doi.org/10.1016/j.rechem.2026.103234
Primary Topic
Protein Degradation and Inhibitors
Type
article
Field-Weighted Citation Impact
0.00
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article

Opportunities and challenges of PROTAC in the treatment of protein-driven diseases

Zhe Zhou, Peng Liu, Xuelian Liu, Jinyao Li et al.
Results in Chemistry
Protein Degradation and Inhibitors
article

Opportunities and challenges of PROTAC in the treatment of protein-driven diseases

Zhe Zhou, Peng Liu, Xuelian Liu, Jinyao Li, Yang Li
article en

Abstract

Targeted protein degradation (TPD) has transformed the landscape of drug discovery by exploiting the ubiquitin-proteasome system (UPS) to eliminate, rather than inhibit, pathogenic proteins. This paradigm shift enables access to a vast array of previously “undruggable” targets and offers new therapeutic opportunities across diverse diseases. Among the available approaches, proteolysis-targeting chimera (PROTAC) have rapidly advanced from concept to clinical evaluation. Here we highlight the unique advantages of PROTAC in disease treatment and target identification, and examine emerging solutions to address key challenges such as pharmacokinetics, E3 ligase diversity, and selectivity. Together, these advances define a new era of precision therapeutics based on the controlled elimination of disease drivers.

Results in ChemistryVol. 24
Xinjiang Institute of Materia Medica (CN), Xinjiang University (CN)
Openalex Percentile: Top 25%
Protein Degradation and Inhibitors
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