TY - JOUR
T1 - RIPTACs
T2 - A groundbreaking approach to drug discovery
AU - Ma, Zonghui
AU - Bolinger, Andrew A.
AU - Zhou, Jia
N1 - Publisher Copyright:
© 2023 Elsevier Ltd
PY - 2023/11
Y1 - 2023/11
N2 - Regulated induced proximity targeting chimeras (RIPTACs), a new class of heterobifunctional molecules, show promise in specifically targeting and eliminating cancer cells while leaving healthy cells unharmed. As a groundbreaking drug discovery approach, RIPTACs work by forming a stable complex with two proteins, one specifically found in cancer cells (target protein, TP) and the other pan-essential for cell survival (effector protein, EP), selectively disrupting the function of the EP in cancer cells and causing cell death. Interestingly, the TPs need not be linked to disease progression, broadening the spectrum of potential drug targets. This review summarizes the discovery and recent advances of the RIPTAC strategy. Additionally, it discusses the associated opportunities and challenges as well as future perspectives in this field.
AB - Regulated induced proximity targeting chimeras (RIPTACs), a new class of heterobifunctional molecules, show promise in specifically targeting and eliminating cancer cells while leaving healthy cells unharmed. As a groundbreaking drug discovery approach, RIPTACs work by forming a stable complex with two proteins, one specifically found in cancer cells (target protein, TP) and the other pan-essential for cell survival (effector protein, EP), selectively disrupting the function of the EP in cancer cells and causing cell death. Interestingly, the TPs need not be linked to disease progression, broadening the spectrum of potential drug targets. This review summarizes the discovery and recent advances of the RIPTAC strategy. Additionally, it discusses the associated opportunities and challenges as well as future perspectives in this field.
KW - RIPTACs
KW - bifunctional molecules
KW - cancer therapy
KW - effector protein (EP)
KW - protein–protein interactions (PPIs)
KW - target protein (TP)
KW - ternary complex
UR - http://www.scopus.com/inward/record.url?scp=85172768414&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85172768414&partnerID=8YFLogxK
U2 - 10.1016/j.drudis.2023.103774
DO - 10.1016/j.drudis.2023.103774
M3 - Review article
C2 - 37734702
AN - SCOPUS:85172768414
SN - 1359-6446
VL - 28
JO - Drug Discovery Today
JF - Drug Discovery Today
IS - 11
M1 - 103774
ER -