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神经元磷酸化蛋白。信号转导的介质。

Neuronal phosphoproteins. Mediators of signal transduction.

作者信息

Greengard P

机构信息

Laboratory of Molecular and Cellular Neuroscience, Rockefeller University, New York, NY 10021.

出版信息

Mol Neurobiol. 1987 Spring-Summer;1(1-2):81-119. doi: 10.1007/BF02935265.

Abstract

This article summarizes some of our knowledge concerning intracellular protein phosphorylation pathways in nerve cells. It also summarizes, very briefly, recent direct experimental evidence involving intracellular injection of protein kinases, protein kinase inhibitors, and substrates, indicating that protein phosphorylation mediates the actions of a variety of neurotransmitters on their target cells. Finally, it summarizes in somewhat greater detail the results of studies of three different types of substrate proteins that appear to regulate different types of biological responses in nerve cells: synapsin I, a substrate protein present in virtually all nerve terminals, which appears to regulate neurotransmitter release from those nerve terminals; the acetylcholine receptor, the phosphorylation of which regulates its rate of desensitization in the presence of acetylcholine; and DARPP-32, the phosphorylation of which converts it into a very potent phosphoprotein phosphatase inhibitor that may be involved in the regulation by the neuromodulator dopamine of the effects of the neurotransmitter glutamate. The identification and characterization of additional neuronal phosphoproteins can be expected to lead to the clarification of numerous additional molecular mechanisms by which signal transduction is carried out in nerve cells.

摘要

本文总结了我们关于神经细胞内蛋白质磷酸化途径的一些知识。它还非常简要地总结了最近的直接实验证据,这些证据涉及细胞内注射蛋白激酶、蛋白激酶抑制剂和底物,表明蛋白质磷酸化介导了多种神经递质对其靶细胞的作用。最后,它更详细地总结了对三种不同类型底物蛋白的研究结果,这些底物蛋白似乎调节神经细胞中不同类型的生物学反应:突触素I,一种几乎存在于所有神经末梢的底物蛋白,它似乎调节这些神经末梢的神经递质释放;乙酰胆碱受体,其磷酸化调节其在乙酰胆碱存在下的脱敏速率;以及DARPP - 32,其磷酸化将其转化为一种非常有效的蛋白磷酸酶抑制剂,可能参与神经调质多巴胺对神经递质谷氨酸作用的调节。预计对其他神经元磷酸化蛋白的鉴定和表征将有助于阐明神经细胞中进行信号转导的众多其他分子机制。

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