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钾离子对NAADP(烟酰胺腺嘌呤二核苷酸磷酸)受体的调节作用:多种NAADP受体构象的证据

Modulation of NAADP (nicotinic acid-adenine dinucleotide phosphate) receptors by K+ ions: evidence for multiple NAADP receptor conformations.

作者信息

Dickinson George D, Patel Sandip

机构信息

The Old Squash Courts, Department of Physiology, University College London, Gower Street, London WC1E 6BT, UK.

出版信息

Biochem J. 2003 Nov 1;375(Pt 3):805-12. doi: 10.1042/BJ20030672.

Abstract

NAADP (nicotinic acid-adenine dinucleotide phosphate) mediates Ca2+ release from intracellular Ca2+ stores in a wide variety of cell types. In sea urchin eggs, subthreshold concentrations of NAADP can cause full inactivation of NAADP-induced Ca2+ release, an effect that may be related to the ability of the target protein to bind its ligand in an essentially irreversible manner. In the present study, we found that K+ ions inhibit dissociation of NAADP from sea urchin egg homogenates. In low K+-containing media, an addition of excess unlabelled NAADP effectively displaced bound radioligand whereas dilution of radioligand initiated only partial dissociation. The inhibitory effects of K+ on dissociation of NAADP were concentration dependent, reversible and persisted after detergent solubilization. Lowering [K+] of the medium decreased the sensitivity of NAADP receptors for their ligand in stimulating Ca2+ release, but it did not affect inactivation of NAADP-induced Ca2+ release by subthreshold concentrations of NAADP. Our results are consistent with the observation of multiple conformations of the NAADP receptor that are readily revealed in low K+-containing media.

摘要

烟酰胺腺嘌呤二核苷酸磷酸(NAADP)在多种细胞类型中介导细胞内钙库释放钙离子。在海胆卵中,阈下浓度的NAADP可导致NAADP诱导的钙离子释放完全失活,这种效应可能与靶蛋白以基本不可逆的方式结合其配体的能力有关。在本研究中,我们发现钾离子抑制NAADP从海胆卵匀浆中的解离。在低钾培养基中,添加过量未标记的NAADP可有效置换结合的放射性配体,而放射性配体的稀释仅引发部分解离。钾离子对NAADP解离的抑制作用呈浓度依赖性、可逆,且在去污剂溶解后仍持续存在。降低培养基中的[K⁺]会降低NAADP受体对其配体刺激钙离子释放的敏感性,但不影响阈下浓度的NAADP对NAADP诱导的钙离子释放的失活作用。我们的结果与在低钾培养基中容易揭示的NAADP受体多种构象的观察结果一致。

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