坦克结合激酶1
IκB激酶
激酶
细胞生物学
干扰素
先天免疫系统
生物
信号转导
磷酸化
蛋白激酶A
分泌物
化学
癌症研究
MAP激酶激酶激酶
受体
生物化学
免疫学
NF-κB
作者
Douglas W. Thomson,Daniel Poeckel,Nico Zinn,Christina Rau,Katrin Strohmer,Anne J. Wagner,Alan P. Graves,Jessica Perrin,Marcus Bantscheff,Birgit Duempelfeld,Viera Kasparcova,Joshi M. Ramanjulu,G. Scott Pesiridis,Marcel Muelbaier,Giovanna Bergamini
标识
DOI:10.1021/acsmedchemlett.9b00027
摘要
The serine/threonine protein kinase TBK1 (Tank-binding Kinase-1) is a noncanonical member of the IkB kinase (IKK) family. This kinase regulates signaling pathways in innate immunity, oncogenesis, energy homeostasis, autophagy, and neuroinflammation. Herein, we report the discovery and characterization of a novel potent and highly selective TBK1 inhibitor, GSK8612. In cellular assays, this small molecule inhibited toll-like receptor (TLR)3-induced interferon regulatory factor (IRF)3 phosphorylation in Ramos cells and type I interferon (IFN) secretion in primary human mononuclear cells. In THP1 cells, GSK8612 was able to inhibit secretion of interferon beta (IFNβ) in response to dsDNA and cGAMP, the natural ligand for STING. GSK8612 is a TBK1 small molecule inhibitor displaying an excellent selectivity profile and therefore represents an ideal probe to further dissect the biology of TBK1 in models of immunity, neuroinflammation, obesity, or cancer.
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