TY - JOUR
T1 - Identification of a new specific Kv1.3 channel blocker, Ctri9577, from the scorpion Chaerilus tricostatus
AU - Xie, Shujun
AU - Feng, Jing
AU - Yu, Congya
AU - Li, Zhi
AU - Wu, Yingliang
AU - Cao, Zhijian
AU - Li, Wenxin
AU - He, Xiaohua
AU - Xiang, Ming
AU - Han, Song
N1 - Funding Information:
This work was supported by grants from the National Basic Research Program of China ( 2010CB529800 ), and the National Science and Technology Major Projects of New Drugs ( 2012ZX09103301-028 ), and the National Natural Sciences Foundation of China to He XH, Li WX and Han S (No. 81171127 ; No. 31071942 ; No. 31000344 ), the Natural Science Foundation of Hubei Province of China ( 2010CDA045 ).
PY - 2012/7
Y1 - 2012/7
N2 - Scorpion toxins are valuable resources for discovering new ion channel modulators and drug candidates. Potassium channel Kv1.3 is an important pharmacological target of T cell-mediated autoimmune diseases, which are encouraging the screening and design of the specific peptide blockers for Kv1.3 channel. Ctri9577, the first neurotoxin gene of Chaerilidae family was cloned from the venom of the scorpion Chaerilus tricostatus through the constructing its cDNA library. The sequence analysis showed that the mature peptide of Ctri9577 contained 39 amino acid residues including six conserved cysteines, whose low sequence similarity indicated that it was a new member of α-KTx15 subfamily. By using expression and purification technology, the recombinant peptide was obtained. Subsequently, the electrophysiological experiments indicated that the Ctri9577 peptide selectively inhibited Kv1.3 channel current with an IC 50 of 0.49 ± 0.45 nM without effectively blocking potassium channels Kv1.1, Kv1.2, hERG and SK3. All these findings not only enrich the knowledge of toxins from the Chaerilidae family, but also present a novel potential drug candidate targeting Kv1.3 channels for the therapy of autoimmune diseases.
AB - Scorpion toxins are valuable resources for discovering new ion channel modulators and drug candidates. Potassium channel Kv1.3 is an important pharmacological target of T cell-mediated autoimmune diseases, which are encouraging the screening and design of the specific peptide blockers for Kv1.3 channel. Ctri9577, the first neurotoxin gene of Chaerilidae family was cloned from the venom of the scorpion Chaerilus tricostatus through the constructing its cDNA library. The sequence analysis showed that the mature peptide of Ctri9577 contained 39 amino acid residues including six conserved cysteines, whose low sequence similarity indicated that it was a new member of α-KTx15 subfamily. By using expression and purification technology, the recombinant peptide was obtained. Subsequently, the electrophysiological experiments indicated that the Ctri9577 peptide selectively inhibited Kv1.3 channel current with an IC 50 of 0.49 ± 0.45 nM without effectively blocking potassium channels Kv1.1, Kv1.2, hERG and SK3. All these findings not only enrich the knowledge of toxins from the Chaerilidae family, but also present a novel potential drug candidate targeting Kv1.3 channels for the therapy of autoimmune diseases.
KW - Autoimmune diseases
KW - Chaerilus tricostatus
KW - Ctri9577
KW - Kv1.3 channel
KW - α-KTx
UR - https://www.scopus.com/pages/publications/84862116420
U2 - 10.1016/j.peptides.2012.04.023
DO - 10.1016/j.peptides.2012.04.023
M3 - Article
C2 - 22580271
AN - SCOPUS:84862116420
SN - 0196-9781
VL - 36
SP - 94
EP - 99
JO - Peptides
JF - Peptides
IS - 1
ER -