Light-activatable photochemically targeting chimeras (PHOTACs) enable the optical control of targeted protein degradation of HDAC6

被引:0
作者
Wurnig, Silas L. [1 ]
Hanl, Maria [1 ]
Geiger, Thomas M. [2 ]
Zhai, Shiyang [1 ]
Dressel, Ina [2 ]
Pienkowska, Dominika E. [2 ]
Nowak, Radoslaw P. [2 ]
Hansen, Finn K. [1 ]
机构
[1] Univ Bonn, Pharmaceut Inst, Dept Pharmaceut & Cell Biol Chem, Immenburg 4, D-53121 Bonn, Germany
[2] Univ Bonn, Inst Struct Biol, Med Fac, Venusberg Campus 1, D-53127 Bonn, Germany
来源
RSC MEDICINAL CHEMISTRY | 2025年
关键词
PROTACS;
D O I
10.1039/d4md00972j
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proteolysis targeting chimeras (PROTACs) are heterobifunctional modalities that induce protein degradation via a catalytic mode of action. Photochemically targeting chimeras (PHOTACs) are a subset of PROTACs designed for light-activated protein degradation, thereby offering precise spatiotemporal control. In this study, we report the design, solid-phase synthesis, and characterization of the first PHOTACs targeting histone deacetylase 6 (HDAC6). We achieved this by incorporating an azobenzene photoswitch into our previously developed HDAC6-selective PROTAC A6. Among the synthesized compounds, PHOTAC 12 demonstrated no HDAC6 degradation in the absence of light but showed significant degradation upon activation to its cis-state with 390 nm light irradiation. Notably, we find that PHOTAC 12 in the cis-state shows significantly improved ternary complex formation compared to the trans-state correlating with its degradation efficacy. Overall, PHOTAC 12 is a promising lead compound for the development of light-activatable HDAC6 degraders.
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页数:8
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