丙戊酸钠(VPA)与组蛋白H1和H3混合物的FTIR光谱数据

M. Mello, B. Vidal
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引用次数: 2

摘要

丙戊酸/丙戊酸钠(VPA)是一种主要用于治疗癫痫的药物,被认为是一种有效的表观遗传药物,可诱导组蛋白去乙酰化酶的抑制,促进DNA和组蛋白甲基化状态的改变,并影响染色质结构。除了这些表观遗传效应外,VPA对组蛋白H1的分子亲和性已经基于热变性、荧光光谱和圆二色性分析提出。最近利用傅里叶变换红外(FTIR)微光谱和高性能偏振显微镜研究了VPA与DNA和组蛋白的相互作用,这些相互作用与表观遗传标记的促进作用无关。本文的数据为更好地理解VPA与组蛋白H1和H3混合物的FTIR光谱以及文献中报道的VPA直接对组蛋白的潜在影响提供了补充信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Data on FTIR spectra of mixtures of sodium valproate (VPA) and histones H1 and H3
Valproic acid/sodium valproate (VPA), a drug primarily used for treatment of seizure disorders, is recognized as an efficient epigenetic agent, inducing inhibition of histone deacetylases, promoting changes in the methylation status of DNA and histones, and affecting chromatin structure. In addition to these epigenetic effects, molecular affinity of VPA for histone H1 has been proposed based on thermal denaturation, fluorescence spectroscopy and circular dichroism assays. VPA interactions with DNA and histones using Fourier transform infrared (FTIR) microspectroscopy and high-performance polarization microscopy that are not related to the effects promoted on epigenetic markers have been recently explored. Data in this article provide supplementary information for a better understanding of the resulting FTIR spectra for mixtures of VPA and histones H1 and H3 and of the potential effect of VPA directly on histones that has been reported in the literature.
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