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Conditional PROTAC: Recent Strategies for Modulating Targeted Protein Degradation.
Yim, Junhyeong; Park, Junyoung; Kim, Gabin; Lee, Hyung Ho; Chung, Jin Soo; Jo, Ala; Koh, Minseob; Park, Jongmin.
Afiliación
  • Yim J; Department of Chemistry, Kangwon National University, Chuncheon, 24341, Republic of Korea.
  • Park J; Multidimensional Genomics Research Center, Kangwon National University, Chuncheon, 24341, Republic of Korea.
  • Kim G; Department of Chemistry, Kangwon National University, Chuncheon, 24341, Republic of Korea.
  • Lee HH; Institute for Molecular Science and Fusion Technology, Kangwon National University, Chuncheon, 24341, Republic of Korea.
  • Chung JS; Department of Chemistry and Chemistry, Institute for Functional Materials, Pusan National University, Busan, 46241, Republic of Korea.
  • Jo A; Department of Urology, Urological Cancer Center, Research Institute and Hospital of National Cancer Center, Goyang, 10408, Republic of Korea.
  • Koh M; Department of Urology, Urological Cancer Center, Research Institute and Hospital of National Cancer Center, Goyang, 10408, Republic of Korea.
  • Park J; Center for Nanomedicine, Institute for Basic Science, Seoul, 03722, Republic of Korea.
ChemMedChem ; : e202400326, 2024 Jul 12.
Article en En | MEDLINE | ID: mdl-38993102
ABSTRACT
Proteolysis-targeting chimeras (PROTACs) have emerged as a promising technology for inducing targeted protein degradation by leveraging the intrinsic ubiquitin-proteasome system (UPS). While the potential druggability of PROTACs toward undruggable proteins has accelerated their rapid development and the wide-range of applications across diverse disease contexts, off-tissue effects and side-effects of PROTACs have recently received attentions to improve their efficacy. To address these issues, spatial or temporal target protein degradation by PROTACs has been spotlighted. In this review, we explore chemical strategies for modulating protein degradation in a cell type-specific (spatio-) and time-specific (temporal-) manner, thereby offering insights for expanding PROTAC applications to overcome the current limitations of target protein degradation strategy.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: ChemMedChem Asunto de la revista: FARMACOLOGIA / QUIMICA Año: 2024 Tipo del documento: Article Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: ChemMedChem Asunto de la revista: FARMACOLOGIA / QUIMICA Año: 2024 Tipo del documento: Article Pais de publicación: Alemania