LIU Jing-hong, CHEN Yi-min, CAI Xiao-qing*. Research advances in new technologies in targeted protein degradationJ. Acta Pharmaceutica Sinica, 2022,57(2): 313-320. doi: 10.16438/j.0513-4870.2021-1249
Citation: LIU Jing-hong, CHEN Yi-min, CAI Xiao-qing*. Research advances in new technologies in targeted protein degradationJ. Acta Pharmaceutica Sinica, 2022,57(2): 313-320. doi: 10.16438/j.0513-4870.2021-1249

Research advances in new technologies in targeted protein degradation

  • In recent years, the targeted protein degradation technology has developed quickly, with proteolysis-targeting chimera (PROTAC) as the best-known strategy through exploring the ubiquitin-proteasome system. A number of new targeted protein degradation strategies have been emerging to expand the scope of protein degradation technology, including lysosome-targeting chimeras (LYTACs), autophagy-targeting chimeras (AUTACs), autophagosome-tethering compounds (ATTECs) and chimeras based on chaperone-mediated autophagy (CMA). The emerging methodologies have explored another important protein degradation system in eukaryotes-lysosomal systems, such as the endosome-lysosome pathway and the autophagy-lysosome pathway. This review summaries the mechanisms and features of different strategies for targeted protein degradation, with a special emphasis on the new targeted protein degradation technologies, such as their current status, advantages and limitations.
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