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乙醇对 Akt 构象变化的影响:化学交联、质谱和(18)O 标记研究。

Effects of ethanol on conformational changes of Akt studied by chemical cross-linking, mass spectrometry, and (18)O labeling.

机构信息

Laboratory of Molecular Signaling, DICBR, NIAAA, National Institutes of Health, Bethesda, Maryland 20892-9410, United States.

出版信息

ACS Chem Biol. 2012 Feb 17;7(2):387-94. doi: 10.1021/cb2003237. Epub 2011 Dec 7.

Abstract

Although PI3K/Akt signaling that regulates neuronal survival has been implicated in the deleterious effects of ethanol on the central nervous system, underlying molecular mechanisms have not been fully elucidated. Akt-membrane interaction is a prerequisite step for Akt activation since it induces interdomain conformational changes to an open conformer that allows Akt phosphorylation by upstream kinases. In this study, we investigated the effect of ethanol on Akt activation by quantitatively probing Akt conformation using chemical cross-linking, (18)O labeling and mass spectrometry. We found that ethanol at pharmacologically relevant concentrations (20 or 170 mM) directly interacts with Akt and alters the local pleckstrin homology domain configuration near the PIP(3)-binding site. We also found that ethanol significantly impairs subsequent membrane-induced interdomain conformational changes needed for Akt activation. The observed alteration of Akt conformation caused by ethanol during the activation sequence provides a new molecular basis for the effects of ethanol on Akt signaling. The in vitro conformation-based approach employed in this study should also be useful in probing the molecular mechanisms for the action of ethanol or drugs on other signaling proteins, particularly for those undergoing dramatic conformational change during activation processes such as members of AGC kinase super family.

摘要

虽然 PI3K/Akt 信号通路调节神经元存活,这与乙醇对中枢神经系统的有害作用有关,但潜在的分子机制尚未完全阐明。Akt-膜相互作用是 Akt 激活的前提步骤,因为它诱导结构域间构象变化为开放构象,从而允许上游激酶对 Akt 进行磷酸化。在这项研究中,我们使用化学交联、(18)O 标记和质谱法定量探测 Akt 构象,研究了乙醇对 Akt 激活的影响。我们发现,在药理学相关浓度(20 或 170 mM)下,乙醇直接与 Akt 相互作用,并改变靠近 PIP(3)结合位点的局部 pleckstrin 同源结构域构象。我们还发现,乙醇显著损害了 Akt 激活所需的后续膜诱导的结构域间构象变化。乙醇在激活过程中对 Akt 构象的观察到的改变为乙醇对 Akt 信号的作用提供了新的分子基础。本研究中采用的基于构象的体外方法也应该有助于探测乙醇或药物对其他信号蛋白作用的分子机制,特别是对于那些在激活过程中经历剧烈构象变化的蛋白,如 AGC 激酶超家族成员。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c125/3475205/c0a2d3532e4e/nihms409025f1.jpg

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