TY - JOUR
T1 - The rise of covalent proteolysis targeting chimeras
AU - Gabizon, Ronen
AU - London, Nir
N1 - NL is the incumbent of the Alan and Laraine Fischer Career Development Chair. NL would like to acknowledge funding from the Israel Science Foundation (grants no. 2462/19 and 3824/19 ), the Israel Cancer Research Fund , the Israeli Ministry of Science Technology (grant no. 3-14763 ), the Israeli ministry of health (grant no. 3-15102 ), the Moross Integrated Cancer Center , and the Barry Sherman institute for Medicinal Chemistry . NL is also supported by the Honey and Dr. Barry Sherman Lab and the Estate of Emile Mimran, Nelson P. Sirotsky, and the Rising Tide Foundation .
PY - 2021/6
Y1 - 2021/6
N2 - Targeted protein degradation offers several advantages over direct inhibition of protein activity and is gaining increasing interest in chemical biology and drug discovery. Proteolysis targeting chimeras (PROTACs) in particular are enjoying widespread application. However, PROTACs, which recruit an E3 ligase for degradation of a target protein, still suffer from certain challenges. These include a limited selection for E3 ligases on the one hand and the requirement for potent target binding on the other hand. Both issues restrict the target scope available for PROTACs. Degraders that covalently engage the target protein or the E3 ligase can potentially expand the pool of both targets and E3 ligases. Moreover, they may offer additional advantages by improving the kinetics of ternary complex formation or by endowing additional selectivity to the degrader. Here, we review the recent progress in the emerging field of covalent PROTACs.
AB - Targeted protein degradation offers several advantages over direct inhibition of protein activity and is gaining increasing interest in chemical biology and drug discovery. Proteolysis targeting chimeras (PROTACs) in particular are enjoying widespread application. However, PROTACs, which recruit an E3 ligase for degradation of a target protein, still suffer from certain challenges. These include a limited selection for E3 ligases on the one hand and the requirement for potent target binding on the other hand. Both issues restrict the target scope available for PROTACs. Degraders that covalently engage the target protein or the E3 ligase can potentially expand the pool of both targets and E3 ligases. Moreover, they may offer additional advantages by improving the kinetics of ternary complex formation or by endowing additional selectivity to the degrader. Here, we review the recent progress in the emerging field of covalent PROTACs.
UR - https://www.scopus.com/pages/publications/85100410353
U2 - 10.1016/j.cbpa.2020.12.003
DO - 10.1016/j.cbpa.2020.12.003
M3 - Review article
SN - 1367-5931
VL - 62
SP - 24
EP - 33
JO - Current Opinion in Chemical Biology
JF - Current Opinion in Chemical Biology
ER -