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钠离子和氯离子对红藻氨酸受体的调制作用。

Kainate receptor modulation by sodium and chloride.

机构信息

Leibniz-Institut für Molekulare Pharmakologie (FMP), Robert-Rössle-Str. 10, 13125, Berlin, Germany.

出版信息

Adv Exp Med Biol. 2011;717:93-113. doi: 10.1007/978-1-4419-9557-5_9.

Abstract

The kainate-type glutamate receptor displays strong modulation by monovalent anions and cations. This modulation is independent of permeation of the ion channel. Instead, structural, computational and biophysical evidence shows that receptor activity is controlled by binding of sodium and chloride ions at sites that stabilize active dimers of glutamate binding domains. Modulation by monovalent ions is a surprisingly general property across ion channel families. However, evidence of a physiological role for ion-dependent effects on glutamate receptors is lacking, perhaps reflecting the adventitious use of ions as structural components of the kainate receptor. "ergo, Hercules, vita humanior sine sale non quit degree […]" "Heaven known, a civilized life is impossible without salt" -Pliny the Elder, Natural History XXXI 88.

摘要

红藻氨酸型谷氨酸受体受到单价阴离子和阳离子的强烈调节。这种调节与离子通道的通透性无关。相反,结构、计算和生物物理证据表明,受体活性受钠离子和氯离子结合在稳定谷氨酸结合域活性二聚体的位点的控制。单价离子的调节是离子通道家族中一种惊人的普遍特性。然而,缺乏离子依赖性对谷氨酸受体的生理作用的证据,这也许反映了红藻氨酸受体将离子作为结构成分的偶然使用。“因此,大力神,没有盐的人生是不完整的 […]” “天知道,没有盐的文明生活是不可能的” -老普林尼,《自然史》XXXI 88。

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