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锌离子和铜离子诱导人β-晶体蛋白聚集。

Zinc and Copper Ions Induce Aggregation of Human β-Crystallins.

机构信息

LABRMN, Centro de Investigaciones Químicas, Instituto de Investigación en Ciencias Básicas y Aplicadas, Universidad Autónoma del Estado de Morelos, Cuernavaca 62209, Mexico.

出版信息

Molecules. 2022 May 6;27(9):2970. doi: 10.3390/molecules27092970.

Abstract

Cataracts are defined as the clouding of the lens due to the formation of insoluble protein aggregates. Metal ions exposure has been recognized as a risk factor in the cataract formation process. The γ and β crystallins are members of a larger family and share several structural features. Several studies have shown that copper and zinc ions induce the formation of γ-crystallins aggregates. However, the interaction of metal ions with β-crystallins, some of the most abundant crystallins in the lens, has not been explored until now. Here, we evaluate the effect of Cu(II) and Zn(II) ions on the aggregation of HβA1, as a representative of the acidic form, and HβB2, as a representative of the basic β-crystallins. We used several biophysical techniques and computational methods to show that Cu(II) and Zn(II) induce aggregation following different pathways. Both metal ions destabilize the proteins and impact protein folding. Copper induced a small conformational change in HβA1, leading to high-molecular-weight light-scattering aggregates, while zinc is more aggressive towards HβB2 and induces a larger conformational change. Our work provides information on the mechanisms of metal-induced aggregation of β-crystallins.

摘要

白内障被定义为晶状体混浊,这是由于不溶性蛋白质聚集体的形成。金属离子暴露已被认为是白内障形成过程中的一个风险因素。γ和β晶状体蛋白是一个更大家族的成员,它们具有几个结构特征。几项研究表明,铜和锌离子诱导γ-晶状体蛋白聚集体的形成。然而,直到现在,金属离子与β-晶状体蛋白的相互作用——β-晶状体蛋白是晶状体中最丰富的晶状体蛋白之一——才被探索。在这里,我们评估了 Cu(II)和 Zn(II)离子对 HβA1(酸性形式的代表)和 HβB2(碱性β-晶状体蛋白的代表)聚集的影响。我们使用了几种生物物理技术和计算方法来表明,Cu(II)和 Zn(II)离子通过不同的途径诱导聚集。这两种金属离子都会使蛋白质失稳并影响蛋白质折叠。铜诱导 HβA1 发生小的构象变化,导致高分子量光散射聚集物,而锌对 HβB2 更具攻击性,诱导更大的构象变化。我们的工作提供了有关金属诱导β-晶状体蛋白聚集机制的信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b981/9105653/2caf4b25f29a/molecules-27-02970-g001.jpg

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