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本文引用的文献

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Activation by G protein beta gamma subunits of beta-adrenergic and muscarinic receptor kinase.G蛋白βγ亚基对β-肾上腺素能受体激酶和毒蕈碱受体激酶的激活作用。
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Activation of the cloned muscarinic potassium channel by G protein beta gamma subunits.G蛋白βγ亚基对克隆的毒蕈碱钾通道的激活作用。
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Activation of a GTP-binding protein and a GTP-binding-protein-coupled receptor kinase (beta-adrenergic-receptor kinase-1) by a muscarinic receptor m2 mutant lacking phosphorylation sites.缺乏磷酸化位点的毒蕈碱受体m2突变体对GTP结合蛋白和GTP结合蛋白偶联受体激酶(β-肾上腺素能受体激酶-1)的激活作用。
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大鼠心房细胞中毒蕈碱钾电流的受体激酶依赖性脱敏

Receptor kinase-dependent desensitization of the muscarinic K+ current in rat atrial cells.

作者信息

Shui Z, Boyett M R, Zang W J, Haga T, Kameyama K

机构信息

Department of Physiology, University of Leeds, UK.

出版信息

J Physiol. 1995 Sep 1;487 ( Pt 2)(Pt 2):359-66. doi: 10.1113/jphysiol.1995.sp020885.

DOI:10.1113/jphysiol.1995.sp020885
PMID:8558469
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1156578/
Abstract
  1. Activity of rat atrial muscarinic K+ channels has been measured in five configurations of the patch clamp technique. 2. In configurations in which the normal intracellular solution was lost, the slow phase of desensitization (a slow decline of channel activity during an exposure to ACh) was much reduced (or absent) and deactivation (on wash-off of ACh) was slowed as compared with desensitization and deactivation in configurations in which normal intracellular solution was retained. This suggests that soluble intracellular regulators are involved in these processes. 3. When a G protein-coupled receptor kinase (GRK2) was applied to the cytoplasmic surface of conventional outside-out patches in the presence of ATP, the slow phase of desensitization was restored. In the absence of ATP, GRK2 failed to restore the slow phase. 4. It is concluded that (i) G protein-coupled receptor kinase dependent phosphorylation of the muscarinic receptor is responsible for the slow phase of desensitization and (ii) a soluble factor (such as a GTPase activating protein or 'GAP') is responsible for normal rapid deactivation.
摘要
  1. 采用膜片钳技术的五种模式测量了大鼠心房毒蕈碱型钾通道的活性。2. 在正常细胞内溶液丢失的模式中,脱敏的慢相(暴露于乙酰胆碱期间通道活性的缓慢下降)大大减少(或不存在),并且与保留正常细胞内溶液的模式中的脱敏和失活相比,失活(乙酰胆碱洗脱时)减慢。这表明可溶性细胞内调节因子参与了这些过程。3. 当在ATP存在的情况下将G蛋白偶联受体激酶(GRK2)应用于传统的外向膜片的细胞质表面时,脱敏的慢相得以恢复。在没有ATP的情况下,GRK2未能恢复慢相。4. 得出的结论是:(i)毒蕈碱型受体的G蛋白偶联受体激酶依赖性磷酸化负责脱敏的慢相,(ii)一种可溶性因子(如GTP酶激活蛋白或“GAP”)负责正常的快速失活。