Discovery of a small-molecule inhibitor of the TRIP8b–HCN interaction with efficacy in neurons

• Published in: The Journal of biological chemistry 2022-07, Vol.298 (7), p.102069-102069, Article 102069
• Main Authors: Han, Ye, Iyamu, Iredia D., Clutter, Matthew R., Mishra, Rama K., Lyman, Kyle A., Zhou, Chengwen, Michailidis, Ioannis, Xia, Maya Y., Sharma, Horrick, Luan, Chi-Hao, Schiltz, Gary E., Chetkovich, Dane M.
• Format: Article
• Language: English
• Subjects: Animals; Cyclic Nucleotide-Gated Cation Channels - metabolism; Depressive Disorder, Major - metabolism; h current; HCN; hippocampus; Hippocampus - metabolism; Humans; Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels - metabolism; major depressive disorder; Mammals - metabolism; Neurons - metabolism; small molecule; TRIP8b
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/j.jbc.2022.102069

Major depressive disorder is a critical public health problem with a lifetime prevalence of nearly 17% in the United States. One potential therapeutic target is the interaction between hyperpolarization-activated cyclic nucleotide–gated (HCN) channels and an auxiliary subunit of the channel named tetratricopeptide repeat–containing Rab8b-interacting protein (TRIP8b). HCN channels regulate neuronal excitability in the mammalian hippocampus, and recent work has established that antagonizing HCN function rescues cognitive impairment caused by chronic stress. Here, we utilize a high-throughput virtual screen to find small molecules capable of disrupting the TRIP8b–HCN interaction. We found that the hit compound NUCC-0200590 disrupts the TRIP8b–HCN interaction in vitro and in vivo. These results provide a compelling strategy for developing new small molecules capable of disrupting the TRIP8b–HCN interaction.