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Biochimica et biophysica acta, General subjects v.1861 no.3, 2017년, pp.615 - 623   SCI SCIE
본 등재정보는 저널의 등재정보를 참고하여 보여주는 베타서비스로 정확한 논문의 등재여부는 등재기관에 확인하시기 바랍니다.

Protein toxins of the Echis coloratus viper venom directly activate TRPV1

Geron, Matan (Corresponding author at: Ein Karem Campus, The Hebrew University of Jerusalem, Jerusalem 91120, Israel. ) ; Kumar, Rakesh ; Matzner, Henry ; Lahiani, Adi ; Gincberg, Galit ; Cohen, Gadi ; Lazarovici, Philip ; Priel, Avi ;
  • 초록  

    Abstract Background Peptide and protein toxins are essential tools to dissect and probe the biology of their target receptors. Venoms target vital physiological processes to evoke pain. Snake venoms contain various factors with the ability to evoke, enhance and sustain pain sensation. While a number of venom-derived toxins were shown to directly target TRPV1 channels expressed on somatosensory nerve terminals to evoke pain response, such toxins were yet to be identified in snake venoms. Methods We screened Echis coloratus saw-scaled viper venom's protein fractions isolated by reversed phase HPLC for their ability to activate TRPV1 channels. To this end, we employed heterologous systems to analyze TRPV1 and NGF pathways by imaging and electrophysiology, combined with molecular biology, biochemical, and pharmacological tools. Results We identified TRPV1 activating proteins in the venom of Echis coloratus that produce a channel-dependent increase in intracellular calcium and outwardly rectifying currents in neurons and heterologous systems. Interestingly, channel activation was not mediated by any of its known toxin binding sites. Moreover, although NGF neurotropic activity was detected in this venom, TRPV1 activation was independent of NGF receptors. Conclusions Echis coloratus venom contains proteins with the ability to directly activate TRPV1. This activity is independent of the NGF pathway and is not mediated by known TRPV1 toxins' binding sites. General significance Our results could facilitate the discovery of new toxins targeting TRPV1 to enhance current understanding of this receptor activation mechanism. Furthermore, the findings of this study provide insight into the mechanism through which snakes' venom elicit pain. Highlights The snake venom from Echis coloratus contains peptides that target TRPV1. TRPV1 activation by this venom is not mediated by known toxins' binding sites. Snake venom elicits pain by directly activating pain receptors. The NGF presence in the venom suggests synergistic effect between its components.


  • 주제어

    Toxins .   Viperidae venom .   Echis coloratus .   TRPV1 .   HPLC protein fraction .   Capsaicin .   NGF .   Live-cell calcium imaging .   Patch clamp technique .   Pain.  

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