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首页> 外文期刊>Archives of Biochemistry and Biophysics >Zinc/thiolate redox biochemistry of metallothionein and the control of zinc ion fluctuations in cell signaling
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Zinc/thiolate redox biochemistry of metallothionein and the control of zinc ion fluctuations in cell signaling

机译:金属硫蛋白的锌/硫醇盐氧化还原生物化学和细胞信号传导中锌离子波动的控制

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摘要

Free zinc ions are potent effectors of proteins. Their tightly controlled fluctuations ("zinc signals") in the picomolar range of concentrations modulate cellular signaling pathways. Sulfur (cysteine) donors generate redox-active coordination environments in proteins for the redox-inert zinc ion and make it possible for redox signals to induce zinc signals. Amplitudes of zinc signals are determined by the cellular zinc buffering capacity, which itself is redox-sensitive. In part by interfering with zinc and redox buffering, reactive species, drugs, toxins, and metal ions can elicit zinc signals that initiate physiological and pathobiochemical changes or lead to cellular injury when free zinc ions are sustained at higher concentrations. These interactions establish redox-inert zinc as an important factor in redox signaling. At the center of zinc/redox signaling are the zinc/thiolate clusters of metallothionein. They can transduce zinc and redox signals and thereby attenuate or amplify these signals. (C) 2007 Elsevier Inc. All rights reserved.
机译:游离锌离子是蛋白质的有效效应器。它们在皮摩尔浓度范围内受到严格控制的波动(“锌信号”)调节细胞信号传导途径。硫(半胱氨酸)供体在蛋白质中为氧化还原惰性的锌离子生成氧化还原活性的配位环境,并使氧化还原信号诱导锌信号成为可能。锌信号的幅度取决于细胞对锌的缓冲能力,而锌缓冲能力本身对氧化还原敏感。通过干扰锌和氧化还原的缓冲作用,部分反应性物质,药物,毒素和金属离子可以引发锌信号,从而启动生理和病理生化变化,或者当游离锌离子保持在较高浓度时会导致细胞损伤。这些相互作用将氧化还原惰性锌确定为氧化还原信号传导中的重要因素。锌/氧化还原信号的中心是金属硫蛋白的锌/硫醇盐簇。它们可以转导锌和氧化还原信号,从而衰减或放大这些信号。 (C)2007 Elsevier Inc.保留所有权利。

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