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Proteomic approaches advancing targeted protein degradation
被引:20
作者:
Sathe, Gajanan
[1
]
Sapkota, Gopal P.
[1
]
机构:
[1] Univ Dundee, Sch Life Sci, MRC Prot Phosphorylat & Ubiquitylat Unit, Dundee DD1 5EH, Scotland
基金:
英国医学研究理事会;
关键词:
CHEMICAL PROBES;
AFFINITY;
PROTACS;
DISCOVERY;
REVEALS;
BINDING;
RECOGNITION;
DEGRADERS;
COMPLEXES;
LIGANDS;
D O I:
10.1016/j.tips.2023.08.007
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Targeted protein degradation (TPD) is an emerging modality for research and therapeutics. Most TPD approaches harness cellular ubiquitin-dependent proteolytic pathways. Proteolysis-targeting chimeras (PROTACs) and molecular glue (MG) degraders (MGDs) represent the most advanced TPD approaches, with some already used in clinical settings. Despite these advances, TPD still faces many challenges, pertaining to both the development of effective, selective, and tissue-penetrant degraders and understanding their mode of action. In this review, we focus on progress made in addressing these challenges. In particular, we discuss the utility and application of recent proteomic approaches as indispensable tools to enable insights into degrader development, including target engagement, degradation selectivity, efficacy, safety, and mode of action.
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页码:786 / 801
页数:16
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