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首页> 外文期刊>Journal of Molecular Liquids >Characterization of human serum albumin modified by hair dye component, 4-chloro-1,2-phenylenediamine: Role in protein aggregation, redox biology and cytotoxicity
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Characterization of human serum albumin modified by hair dye component, 4-chloro-1,2-phenylenediamine: Role in protein aggregation, redox biology and cytotoxicity

机译:用染发组分改性人血清白蛋白的表征,4-氯-1,2-苯二胺:在蛋白质聚集,氧化还原生物学和细胞毒性中的作用

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Hair dyes and their components have been described asmutagenic and carcinogenic. They penetrate the skin, undergo auto-oxidation, yield protein reactive derivatives and modify proteins in an irreversible manner. Investigations into the impact of aromatic diamines on protein structures are expected to have a significant clinical value. This study documents the strong potential of 4-chloro-1, 2-phenylenediamine (4-Cl-o-PDA), a hair dye component, in the modification of human serum albumin (HSA). HSA wasmodified in vitro by 4-Cl-o-PDA and changes in tertiary and secondary structural characteristicswere analyzed by UV-visible, fluorescence and far UV circular dichroism, fourier transform infrared spectroscopical techniques and ANS binding assay. Interaction of 4-Cl-oPDA and HSAwas studied bymolecular docking and drug displacement assay. Formation of aggregates and inhibitory effect of antioxidant curcumin was analyzed by ThT binding assay, ThT fluorescence and electron microscopy. Changes in oxidation status of HSA were studied by thiol estimation and NBT assay. Effect of 4-Cl-o-PDA on cellular redox status, DNA integrity and cytotoxicity was analyzed in lymphocytes using dichlorofluorescein method, comet assay andMTT assay. We observed gross structural damage in HSAmodified by 4-Cl-o-PDA. Modification led to unmasking of hydrophobic clusters, loss of its alpha helix and an increase in beta strand and unordered structure in HSA. 4-Cl-o-PDA strongly binds at sub-domain IB of HSA. HSA modified by 4-Cl-o- PDA formed amyloid fibrillar aggregates, whose formation was inhibited by antioxidant treatment. Modified HSA showed reduction of free sulfydryl content. 4-Cl-o-PDA-HSA led to the generation of reactive oxygen species in human lymphocytes. Modified HSA caused an increase in the tail length ofDNA indicating enhanced single strand DNA breaks in cells. Modified protein was found to be genotoxic and cytotoxic. This works offers insights in the role of hair dye components in the biological world. (C) 2021 Elsevier B.V. All rights reserved.
机译:染发剂及其成分被描述为致突变和致癌物质。它们穿透皮肤,经历自动氧化,产生蛋白质反应性衍生物,并以不可逆的方式修饰蛋白质。研究芳香二胺对蛋白质结构的影响有望具有重要的临床价值。本研究记录了染发剂成分4-氯-1,2-苯二胺(4-Cl-o-PDA)在修饰人血清白蛋白(HSA)方面的强大潜力。用4-Cl-o-PDA在体外修饰HSA,并通过紫外可见光谱、荧光光谱和远紫外圆二色谱、傅里叶变换红外光谱技术和ANS结合试验分析三级和二级结构特征的变化。通过分子对接和药物置换实验研究了4-Cl-oPDA和HSAwas的相互作用。通过ThT结合试验、ThT荧光和电子显微镜分析了聚集体的形成和抗氧化剂姜黄素的抑制作用。通过硫醇估算和NBT分析研究了HSA氧化状态的变化。采用二氯荧光素法、彗星试验和MTT法分析4-Cl-o-PDA对淋巴细胞氧化还原状态、DNA完整性和细胞毒性的影响。我们在4-Cl-o-PDA修饰的HSA中观察到了严重的结构损伤。修饰导致疏水性簇的暴露,其α螺旋的丢失,以及HSA中β链和无序结构的增加。4-Cl-o-PDA在HSA的亚结构域IB处强结合。经4-Cl-o-PDA修饰的HSA形成淀粉样纤维聚集体,其形成受到抗氧化剂处理的抑制。改性HSA的游离巯基含量降低。4-Cl-o-PDA-HSA导致人淋巴细胞产生活性氧。修饰的HSA导致DNA的尾部长度增加,表明细胞中单链DNA断裂增强。经修饰的蛋白质具有遗传毒性和细胞毒性。这项研究为染发剂成分在生物世界中的作用提供了见解。(c)2021爱思唯尔B.V.保留所有权利。

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