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通过[3H]维斯阿米醇结合检测到的囊泡乙酰胆碱转运体的多种质子化状态

Multiple protonation states of vesicular acetylcholine transporter detected by binding of [3H]vesamicol.

作者信息

Khare Parul, White Aubrey R, Parsons Stanley M

机构信息

Department of Chemistry and Biochemistry, Neuroscience Research Institute, University of California, Santa Barbara, California 93106, USA.

出版信息

Biochemistry. 2009 Sep 29;48(38):8965-75. doi: 10.1021/bi900759v.

Abstract

Vesicular acetylcholine transporter (VAChT) is inhibited by (-)-vesamicol [(-)-trans-2-(4-phenylpiperidino)cyclohexanol], which binds tightly to an allosteric site. The tertiary alkylamine center in (-)-vesamicol is protonated and positively charged at acidic and neutral pH and unprotonated and uncharged at alkaline pH. Deprotonation of the amine has been taken to explain loss of (-)-vesamicol binding at alkaline pH. However, binding data deviate from a stereotypical bell shape, and more binding occurs than expected at alkaline pH. The current study characterizes the binding of (-)-vesamicol from pH 5 to pH 10 using filter assays, (-)-[3H]vesamicol (hereafter called [3H]vesamicol), and human VAChT expressed in PC12(A123.7) cells. At acidic pH, protons and [3H]vesamicol compete for binding to VAChT. Preexposure or long-term exposure of VAChT to high pH does not affect binding, thus eliminating potential denaturation of VAChT and failure of the filter assay. The dissociation constant for the complex between protonated [3H]vesamicol and VAChT decreases from 12 nM at neutral pH to 2.1 nM at pH 10. The simplest model of VAChT that explains the behavior requires a proton at site 1 to dissociate with pK1 = 6.5 +/- 0.1, a proton at site A to dissociate with pKA = 7.6 +/- 0.2, and a proton at site B to dissociate with pKB = 10.0 +/- 0.1. Deprotonation of the site 1 proton is obligatory for [3H]vesamicol binding. Deprotonation of site A decreases affinity (2.2 +/- 0.5)-fold, and deprotonation of site B increases affinity (18 +/- 4)-fold. Time-dependent dissociation of bound [3H]vesamicol is biphasic, but equilibrium saturation curves are not. The contrasting phasicity suggests that the pathway to and from the [3H]vesamicol binding site exists in open and at least partially closed states. The potential significance of the findings to development of PET and SPECT ligands based on (-)-vesamicol for human diagnostics also is discussed.

摘要

囊泡乙酰胆碱转运体(VAChT)受到(-)-维司卡米[(-)-反式-2-(4-苯基哌啶基)环己醇]的抑制,(-)-维司卡米紧密结合于变构位点。(-)-维司卡米中的叔胺中心在酸性和中性pH下质子化并带正电荷,在碱性pH下未质子化且不带电荷。胺的去质子化被用来解释(-)-维司卡米在碱性pH下结合的丧失。然而,结合数据偏离了典型的钟形,并且在碱性pH下发生的结合比预期的更多。当前研究使用过滤分析法、(-)-[3H]维司卡米(以下称为[3H]维司卡米)以及在PC12(A123.7)细胞中表达的人VAChT来表征pH 5至pH 10条件下(-)-维司卡米的结合情况。在酸性pH下,质子和[3H]维司卡米竞争与VAChT的结合。将VAChT预先暴露或长期暴露于高pH不会影响结合,从而消除了VAChT潜在的变性以及过滤分析的失败。质子化的[3H]维司卡米与VAChT之间复合物的解离常数从中性pH下的12 nM降至pH 10下的2.1 nM。解释该行为的最简单的VAChT模型要求位点1处的一个质子以pK1 = 6.5±0.1的解离常数解离,位点A处的一个质子以pKA = 7.6±0.2的解离常数解离,位点B处的一个质子以pKB = 10.0±0.1的解离常数解离。位点1质子的去质子化是[3H]维司卡米结合所必需的。位点A的去质子化使亲和力降低(2.2±0.5)倍,位点B的去质子化使亲和力增加(18±4)倍。结合的[3H]维司卡米的时间依赖性解离是双相的,但平衡饱和曲线并非如此。这种不同的相性表明通往和离开[3H]维司卡米结合位点的途径存在开放和至少部分关闭的状态。还讨论了这些发现对于基于(-)-维司卡米开发用于人类诊断的PET和SPECT配体的潜在意义。

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