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Assays and technologies for developing proteolysis targeting chimera degraders.
Liu, Xingui; Zhang, Xuan; Lv, Dongwen; Yuan, Yaxia; Zheng, Guangrong; Zhou, Daohong.
Affiliation
  • Liu X; Department of Pharmacodynamics, College of Pharmacy, University of Florida, 1333 Center Drive, Gainesville, FL 32610, USA.
  • Zhang X; Department of Medicinal Chemistry, College of Pharmacy, University of Florida, 1333 Center Drive, Gainesville, FL 32610, USA.
  • Lv D; Department of Pharmacodynamics, College of Pharmacy, University of Florida, 1333 Center Drive, Gainesville, FL 32610, USA.
  • Yuan Y; Department of Pharmacodynamics, College of Pharmacy, University of Florida, 1333 Center Drive, Gainesville, FL 32610, USA.
  • Zheng G; Department of Medicinal Chemistry, College of Pharmacy, University of Florida, 1333 Center Drive, Gainesville, FL 32610, USA.
  • Zhou D; Department of Pharmacodynamics, College of Pharmacy, University of Florida, 1333 Center Drive, Gainesville, FL 32610, USA.
Future Med Chem ; 12(12): 1155-1179, 2020 06.
Article in En | MEDLINE | ID: mdl-32431173
Targeted protein degradation by small-molecule degraders represents an emerging mode of action in drug discovery. Proteolysis targeting chimeras (PROTACs) are small molecules that can recruit an E3 ligase and a protein of interest (POI) into proximity, leading to induced ubiquitination and degradation of the POI by the proteasome system. To date, the design and optimization of PROTACs remain empirical due to the complicated mechanism of induced protein degradation. Nevertheless, it is increasingly appreciated that profiling step-by-step along the ubiquitin-proteasome degradation pathway using biochemical and biophysical assays are essential in understanding the structure-activity relationship and facilitating the rational design of PROTACs. This review aims to summarize these assays and to discuss the potential of expanding the toolbox with other new techniques.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Small Molecule Libraries / Proteolysis Limits: Humans Language: En Journal: Future Med Chem Year: 2020 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Small Molecule Libraries / Proteolysis Limits: Humans Language: En Journal: Future Med Chem Year: 2020 Document type: Article Affiliation country: United States Country of publication: United kingdom