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Intermediate closed channel state(s) precede(s) activation in the ATP-gated P2X2 receptor

机译:在ATP门控的P2X2受体中激活之前,存在中间闭合通道状态

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The molecular mechanism underlying channel opening in response to agonist binding remains a challenging issue in neuroscience. In this regard, many efforts have been recently undertaken in ATP-gated P2X receptors. Among those efforts, we have provided evidence in the P2X2 receptor that tightening of ATP sites upon agonist binding induces opening of the ion channel. Here we extend our analysis to show that the sulfhydryl-reactive ATP analog 8-thiocyano-ATP (NCS-ATP), a potent P2X2 agonist, when covalently labeled in the ATP-binding site at position Leu186 likely favors the tightening mechanism, but not the channel opening mechanism. Our data predict the existence of intermediate or preactivation state(s) trapped by NCS-ATP, in which tightening of the binding site is favored while the channel is still closed. We propose that this (these) intermediate ATP-bound state(s) prime(s) channel gating in the P2X2 receptor.
机译:响应激动剂结合而通道开放的分子机制仍然是神经科学中一个具有挑战性的问题。在这方面,最近已经对ATP门控的P2X受体进行了许多努力。在这些努力中,我们已经在P2X2受体中提供了证据,即激动剂结合后ATP位点的收紧会导致离子通道的打开。在这里,我们扩展分析以表明,当在Leu186位置的ATP结合位点共价标记巯基反应性ATP类似物8-硫氰基ATP(NCS-ATP)(一种强效的P2X2激动剂)时,它可能有利于拧紧机制,但不是渠道开放机制。我们的数据预测存在被NCS-ATP捕获的中间或预激活状态,在这种状态下,尽管通道仍然关闭,但有利于结合位点的收紧。我们建议,在这些P2X2受体中,这些(这些)中间ATP结合状态引发通道门控。

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