Centipede KCNQ Inhibitor SsTx Also Targets K<sub>V</sub>1.3
Canwei Du,
Jiameng Li,
Zicheng Shao,
James Mwangi,
Runjia Xu,
Huiwen Tian,
Guoxiang Mo,
Ren Lai,
Shilong Yang
Affiliations
Canwei Du
College of Life Sciences, Nanjing Agricultural University, Nanjing 210095, Jiangsu, China
Jiameng Li
College of Life Sciences, Nanjing Agricultural University, Nanjing 210095, Jiangsu, China
Zicheng Shao
College of Life Sciences, Nanjing Agricultural University, Nanjing 210095, Jiangsu, China
James Mwangi
Key Laboratory of Animal Models and Human Disease Mechanisms of Chinese Academy of Sciences/Yunnan Province, Kunming Institute of Zoology, Kunming 650223, Yunnan, China
Runjia Xu
College of Life Sciences, Nanjing Agricultural University, Nanjing 210095, Jiangsu, China
Huiwen Tian
College of Life Sciences, Nanjing Agricultural University, Nanjing 210095, Jiangsu, China
Guoxiang Mo
College of Life Sciences, Nanjing Agricultural University, Nanjing 210095, Jiangsu, China
Ren Lai
College of Life Sciences, Nanjing Agricultural University, Nanjing 210095, Jiangsu, China
Shilong Yang
Key Laboratory of Animal Models and Human Disease Mechanisms of Chinese Academy of Sciences/Yunnan Province, Kunming Institute of Zoology, Kunming 650223, Yunnan, China
It was recently discovered that Ssm Spooky Toxin (SsTx) with 53 residues serves as a key killer factor in red-headed centipede’s venom arsenal, due to its potent blockage of the widely expressed KCNQ channels to simultaneously and efficiently disrupt cardiovascular, respiratory, muscular, and nervous systems, suggesting that SsTx is a basic compound for centipedes’ defense and predation. Here, we show that SsTx also inhibits KV1.3 channel, which would amplify the broad-spectrum disruptive effect of blocking KV7 channels. Interestingly, residue R12 in SsTx extends into the selectivity filter to block KV7.4, however, residue K11 in SsTx replaces this ploy when toxin binds on KV1.3. Both SsTx and its mutant SsTx_R12A inhibit cytokines production in T cells without affecting the level of KV1.3 expression. The results further suggest that SsTx is a key molecule for defense and predation in the centipedes’ venoms and it evolves efficient strategy to disturb multiple physiological targets.
