1. Academic Validation
  2. Non-invasive in vivo monitoring of PROTAC-mediated protein degradation using an environment-sensitive reporter

Non-invasive in vivo monitoring of PROTAC-mediated protein degradation using an environment-sensitive reporter

  • Nat Commun. 2025 Feb 22;16(1):1892. doi: 10.1038/s41467-025-57191-0.
Tao Li # 1 Qingyu Zong # 1 He Dong 1 Ihsan Ullah 1 Zhenhai Pan 1 Youyong Yuan 2 3 4
Affiliations

Affiliations

  • 1 School of Biomedical Sciences and Engineering, Guangzhou International Campus, South China University of Technology, Guangzhou, PR China.
  • 2 School of Biomedical Sciences and Engineering, Guangzhou International Campus, South China University of Technology, Guangzhou, PR China. yuanyy@scut.edu.cn.
  • 3 National Engineering Research Center for Tissue Restoration and Reconstruction, South China University of Technology, Guangzhou, PR China. yuanyy@scut.edu.cn.
  • 4 Key Laboratory of Biomedical Engineering of Guangdong Province, South China University of Technology, Guangzhou, PR China. yuanyy@scut.edu.cn.
  • # Contributed equally.
Abstract

Proteolysis targeting chimeras (PROTACs) represent a groundbreaking therapeutic technology for selectively degrading proteins of interest (POIs). The structural variations in PROTACs unpredictably influence their protein degradation efficiency, which is predominantly assessed by quantifying POIs abundance through western blotting. This approach, however, falls short of enabling non-invasive monitoring of protein degradation within living cells let alone assessing directly the degradation effects in vivo. Herein, we develop an environment-sensitive reporter (ESR) for the quantification of protein degradation events triggered by PROTACs in vivo. By simultaneously integrating POIs targeting ligand and an environment-sensitive fluorophore, the ESR signals exhibit a strong fluorescence correlation with the levels of POIs. This non-invasive monitoring reporter offers a high-throughput and convenient way to screen POIs targeting degraders and predict PROTACs-mediated therapeutic outcomes in mouse models. These properties suggest the potential of ESR strategy as a general modular scheme for non-invasive quantification of protein degradation of cancer-related therapeutic targets.

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