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A centipede toxin causes rapid desensitization of nociceptor TRPV1 ion channel

机译:蜈蚣毒素导致Nociceptor TRPV1离子通道的快速脱敏

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摘要

The nociceptive transient receptor potential vanilloid 1 (TRPV1) ion channel is a polymodal receptor for multiple painful stimuli, hence actively pursued as a target for analgesic drugs. We identified a small peptide toxin RhTx2 from the Chinese red-headed centipede that strongly modulates TRPV1 activities. RhTx2, a 31-amino-acid peptide, is similar to a TRPV1-activating toxin RhTx we have previously discovered but with four extra amino acids at the N terminus. We observed that, like RhTx, RhTx2 activated TRPV1, but RhTx2 rapidly desensitized the channel upon prolonged exposure. Desensitization was achieved by reducing both the open probability and the single-channel conductance. RhTx2 is not only a tool to study the desensitization mechanism of TRPV1, but also a promising starting molecule for developing novel analgesics.
机译:Nociceptive瞬态受体潜在的香草素1(TRPV1)离子通道是多种疼痛刺激的多种聚合物受体,因此主动追求作为镇痛药的靶标。 我们鉴定了来自中国红头蜈蚣的小肽毒素rhtx2,强烈调节TRPV1活动。 rHTX2,一种31-氨基酸肽类似于TRPV1 - 活化毒素RHTX,我们先前已经发现,但在N末端具有四种额外的氨基酸。 我们观察到,如rhTX,rhTX2激活的TRPV1,但在长时间暴露时,rhTX2快速脱敏了通道。 通过降低开放概率和单通道电导来实现脱敏。 RHTX2不仅是研究TRPV1的脱敏机制的工具,而且是用于开发新型镇痛药的有前途的起始分子。

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