Assays and technologies for developing proteolysis targeting chimera degraders

Xingui Liu, Xuan Zhang, Dongwen Lv, Yaxia Yuan, Guangrong Zheng, Daohong Zhou

Producción científica: Review articlerevisión exhaustiva

43 Citas (Scopus)

Resumen

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.

Idioma originalEnglish (US)
Páginas (desde-hasta)1155-1179
Número de páginas25
PublicaciónFuture Medicinal Chemistry
Volumen12
N.º12
DOI
EstadoPublished - jun 2020
Publicado de forma externa

ASJC Scopus subject areas

  • Drug Discovery
  • Molecular Medicine
  • Pharmacology

Huella

Profundice en los temas de investigación de 'Assays and technologies for developing proteolysis targeting chimera degraders'. En conjunto forman una huella única.

Citar esto