Literature DB >> 19463735

Expression and characterization of jingzhaotoxin-34, a novel neurotoxin from the venom of the tarantula Chilobrachys jingzhao.

Jinjun Chen1, Yongqun Zhang, Mingqiang Rong, Liqun Zhao, Liping Jiang, Dongyi Zhang, Meichi Wang, Yucheng Xiao, Songping Liang.   

Abstract

Jingzhaotoxin-34 (JZTX-34) is a 35-residue polypeptide from the venom of Chinese tarantula Chilobrachys jingzhao. Our previous work reported its full-length cDNA sequence encoding a precursor with 87 residues. In this study we report the protein expression and biological function characterization. The toxin was efficiently expressed by the secretary pathway in yeast. Under whole-cell patch-clamp mode, the expressed JZTX-34 was able to inhibit tetrodotoxin-sensitive (TTX-S) sodium currents (IC(50) approximately 85 nM) while having no significant effects on tetrodotoxin-resistant (TTX-R) sodium currents on rat dorsal root ganglion neurons. The inhibition of TTX-S sodium channels was completely reversed by strong depolarization (+120 mV). Toxin treatment altered neither channel activation and inactivation kinetics nor recovery rate from inactivation. However, it is interesting to note that in contrast to huwentoxin-IV, a recently identified receptor site-4 toxin from Ornithoctonus huwena venom, 100 nM JZTX-34 caused a negative shift of steady-state inactivation curve of TTX-S sodium channels by approximately 10 mV. The results indicated that JZTX-34 might inhibit mammalian sensory neuronal sodium channels through a mechanism similar to HWTX-IV by trapping the IIS4 voltage sensor in the resting conformation, but their binding sites should not overlay completely.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19463735     DOI: 10.1016/j.peptides.2009.02.018

Source DB:  PubMed          Journal:  Peptides        ISSN: 0196-9781            Impact factor:   3.750


  7 in total

1.  Modulatory features of the novel spider toxin μ-TRTX-Df1a isolated from the venom of the spider Davus fasciatus.

Authors:  Fernanda C Cardoso; Zoltan Dekan; Jennifer J Smith; Jennifer R Deuis; Irina Vetter; Volker Herzig; Paul F Alewood; Glenn F King; Richard J Lewis
Journal:  Br J Pharmacol       Date:  2017-06-27       Impact factor: 8.739

2.  Discovery of a selective NaV1.7 inhibitor from centipede venom with analgesic efficacy exceeding morphine in rodent pain models.

Authors:  Shilong Yang; Yao Xiao; Di Kang; Jie Liu; Yuan Li; Eivind A B Undheim; Julie K Klint; Mingqiang Rong; Ren Lai; Glenn F King
Journal:  Proc Natl Acad Sci U S A       Date:  2013-09-30       Impact factor: 11.205

3.  Native pyroglutamation of huwentoxin-IV: a post-translational modification that increases the trapping ability to the sodium channel.

Authors:  Mingqiang Rong; Zhigui Duan; Juliang Chen; Jianglin Li; Yuchen Xiao; Songping Liang
Journal:  PLoS One       Date:  2013-06-24       Impact factor: 3.240

4.  Customized SmartPeg for measurement of resonance frequency of mini dental implants.

Authors:  Jagjit Singh Dhaliwal; Rubens F Albuquerque; Ali Fakhry; Sukhbir Kaur; Jocelyne S Feine
Journal:  Int J Implant Dent       Date:  2017-02-01

Review 5.  Pain-related toxins in scorpion and spider venoms: a face to face with ion channels.

Authors:  Sylvie Diochot
Journal:  J Venom Anim Toxins Incl Trop Dis       Date:  2021-12-06

6.  Selective Closed-State Nav1.7 Blocker JZTX-34 Exhibits Analgesic Effects against Pain.

Authors:  Xiongzhi Zeng; Pengpeng Li; Bo Chen; Juan Huang; Ren Lai; Jingze Liu; Mingqiang Rong
Journal:  Toxins (Basel)       Date:  2018-02-02       Impact factor: 4.546

Review 7.  Spider Knottin Pharmacology at Voltage-Gated Sodium Channels and Their Potential to Modulate Pain Pathways.

Authors:  Yashad Dongol; Fernanda Caldas Cardoso; Richard J Lewis
Journal:  Toxins (Basel)       Date:  2019-10-29       Impact factor: 4.546

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.