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铕十钨酸盐与组蛋白 H1 的分子相互作用及其作为新型生物标记试剂的应用。

Molecular interaction between europium decatungstate and histone H1 and its application as a novel biological labeling agent.

机构信息

Key Laboratory of Green Process Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, 100190, China.

出版信息

J Biol Inorg Chem. 2010 Sep;15(7):1079-85. doi: 10.1007/s00775-010-0667-5. Epub 2010 May 5.

Abstract

Polyoxometalates (POMs) show promising biological activities, but the mechanism of potential therapeutic effects remains to be elucidated at a molecular level. As a step toward the elucidation of the mechanistic pathways governing the bioactivity of POMs, the interaction between Eu-containing decatungstate [EuW10O36]9- (EuW10) and histone H1 has been studied. Fluorescence/luminescence analysis showed the existence of a strong interaction between EuW10 and histone H1. This interaction has key effects both on the luminescence of EuW10 and on the structure of histone H1. A gradual and intense enhancement of EuW10 luminescence was observed upon addition of increasing concentrations of histone H1. Circular dichroism investigations indicated that the binding of EuW10 significantly alters the secondary structure of histone H1. The present work is meaningful in finding novel labeling agents for fluorescence/luminescence or solid-state bioimaging.

摘要

多金属氧酸盐(POMs)表现出有前景的生物活性,但潜在治疗效果的机制仍需在分子水平上阐明。作为阐明控制 POMs 生物活性的机制途径的一步,研究了含铕的十钨酸盐[EuW10O36]9-(EuW10)与组蛋白 H1 之间的相互作用。荧光/发光分析表明,EuW10 和组蛋白 H1 之间存在强烈的相互作用。这种相互作用对 EuW10 的发光和组蛋白 H1 的结构都有重要影响。随着组蛋白 H1 浓度的增加,观察到 EuW10 发光逐渐增强。圆二色性研究表明,EuW10 的结合显著改变了组蛋白 H1 的二级结构。这项工作对于寻找用于荧光/发光或固态生物成像的新型标记剂具有重要意义。

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