1. Academic Validation
  2. Hydrophobic tag-based protein degradation: Development, opportunity and challenge

Hydrophobic tag-based protein degradation: Development, opportunity and challenge

  • Eur J Med Chem. 2023 Nov 15:260:115741. doi: 10.1016/j.ejmech.2023.115741.
Qindi He 1 Xiaofei Zhao 1 Donglin Wu 1 Siming Jia 1 Canlin Liu 1 Zitian Cheng 1 Fei Huang 1 Yadong Chen 2 Tao Lu 3 Shuai Lu 4
Affiliations

Affiliations

  • 1 School of Science, China Pharmaceutical University, Nanjing, 211198, PR China.
  • 2 Laboratory of Molecular Design and Drug Discovery, China Pharmaceutical University, Nanjing, 211198, PR China. Electronic address: [email protected].
  • 3 State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, 210009, PR China. Electronic address: [email protected].
  • 4 School of Science, China Pharmaceutical University, Nanjing, 211198, PR China. Electronic address: [email protected].
Abstract

Targeted protein degradation (TPD) has emerged as a promising approach for drug development, particularly for undruggable targets. TPD technology has also been instrumental in overcoming drug resistance. While some TPD molecules utilizing proteolysis-targeting chimera (PROTACs) or molecular glue strategies have been approved or evaluated in clinical trials, hydrophobic tag-based protein degradation (HyT-PD) has also gained significant attention as a tool for medicinal chemists. The increasing number of reported HyT-PD molecules possessing high efficiency in degrading protein and good pharmacokinetic (PK) properties, has further fueled interest in this approach. This review aims to present the design rationale, hydrophobic tags in use, and diverse mechanisms of action of HyT-PD. Additionally, the advantages and disadvantages of HyT-PD in protein degradation are discussed. This review may help inspire the development of more HyT-PDs with superior drug-like properties for clinical evaluation.

Keywords

Degradation mechanism; Drug likeness; Hydrophobic tag; Protein degradation; Toxicity.

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