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过氧化氢对人γS-晶状体蛋白的结构、稳定性和聚集特性的影响。

Impact of hydrogen peroxide on structure, stability, and aggregational properties of human γS-crystallin.

作者信息

Vendra Venkata Pulla Rao

机构信息

Ophthalmic Molecular Genetics Section, Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD, USA.

出版信息

J Biosci. 2023;48.

Abstract

Cataract is the leading cause of blindness worldwide. Oxidative stress is one of the known risk factors for agerelated cataracts. The present study was designed to understand the effect of HO-induced oxidative stress on human γS-crystallin and its relationship to lens opacification and cataract. Human γS-crystallin cDNA was cloned into the pET-20b vector, overexpressed in BL21 Star (DE3) cells, and was purified using ion-exchange and gel filtration chromatography. The structure, stability, and aggregational properties of human γS-crystallin under HO stress were studied using fluorescence and circular dichroism spectroscopy methods. HO treatment did not show any significant effect on the γS-crystallin secondary structure but showed an effect on its tertiary structure, resulting in N'-formylkynurenine formation. The HO-treated sample showed increased surface hydrophobicity, was less stable, and opened its Greek key motifs earlier with a midpoint of thermal unfolding curve (T) of 70.2°C compared with untreated γS-crystallin (T=71.4°C). The sample treated with HO aggregated earlier in response to heating at 65°C. HO-induced oxidative stress alters the tryptophan microenvironment and the surface hydrophobicity of γS-crystallin, and these changes decrease its thermal stability and increase its tendency to aggregate, consistent with its role as a risk factor in age-related cataract.

摘要

白内障是全球失明的主要原因。氧化应激是年龄相关性白内障已知的危险因素之一。本研究旨在了解过氧化氢(HO)诱导的氧化应激对人γS-晶状体蛋白的影响及其与晶状体混浊和白内障的关系。将人γS-晶状体蛋白cDNA克隆到pET-20b载体中,在BL21 Star (DE3)细胞中过表达,并用离子交换和凝胶过滤色谱法进行纯化。使用荧光和圆二色光谱法研究了HO应激下人γS-晶状体蛋白的结构、稳定性和聚集特性。HO处理对γS-晶状体蛋白的二级结构没有显著影响,但对其三级结构有影响,导致N'-甲酰犬尿氨酸的形成。HO处理的样品表面疏水性增加,稳定性降低,与未处理的γS-晶状体蛋白(T = 71.4°C)相比,其希腊钥匙基序更早打开,热解链曲线中点(T)为70.2°C。HO处理的样品在65°C加热时更早聚集。HO诱导的氧化应激改变了γS-晶状体蛋白的色氨酸微环境和表面疏水性,这些变化降低了其热稳定性并增加了其聚集倾向,这与其作为年龄相关性白内障危险因素的作用一致。

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