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谷胱甘肽、半胱氨酸和 D-青霉胺在白蛋白金属配合物中交换银金属的作用。

Glutathione, Cysteine, and D-Penicillamine Role in Exchange of Silver Metal from the Albumin Metal Complex.

机构信息

Department of Medical Laboratory Sciences, College of Applied Medical Sciences, Prince Sattam Bin Abdulaziz University, Al-Kharj 11942, Saudi Arabia.

Gomal Centre of Pharmaceutical Sciences Faculty of Pharmacy Gomal University D.I. Khan, 29111, Pakistan.

出版信息

Biomed Res Int. 2022 Aug 8;2022:3619308. doi: 10.1155/2022/3619308. eCollection 2022.

Abstract

The purpose of this study is to investigate the exchange reaction taking place among the bovine serum albumin (BSA), 5,5'-dithiobis-(2-nitrobenzoic acid (ESSE), reduced glutathione, N-acetylcysteine, D-penicillamine (thiolates), and silver metal (Ag). For this purpose, stock solutions of BSA and Ellman's reagent were prepared by dissolving 264 mg of BSA in 5 ml of reaction buffer (0.1 M KHPO at pH 7.8) and 23.8 mg of ESSE in 1.0 ml of reaction buffer which were mixed together. Mixture of BSA-Ag was prepared in a separate procedure by dissolving 0.17 mg of silver nitrate in 1 ml of reaction buffer and then dissolving BSA (200 mg) in the same solution of silver nitrate. Blocking of Cys-34 of BSA with Ag was confirmed by treating different dilutions of BSA-Ag (500 M) solutions with the solutions of ESSE (85 M) and ES (85 M) and recording the spectra (300-450) with a UV-visible spectrophotometer. The chromatographed Ag-modified BSA ((BSA-S)Ag)) samples (typically 500 M) were subsequently mixed with thiolates (reduced glutathione, N-acetylcysteine, and D-penicillamine). Ag and modified BSA (typically 500 M each) were treated with these low molecular weight thiolates and allowed to react overnight followed by chromatographic separation (Sephadex G25). The redox reactions of Ag-modified BSA with various low molecular weight thiols revealed a mechanically important phenomenon. In the case of reduced glutathione and N-acetylcysteine, we observed the rapid release of a commensurate amount of Ellman's anion, indicating that an exchange has taken place and low molecular weight thiols (RSH) substituted Ag species at the Cys-34 of BSA eventually forming disulfide (BSA-SSR) at Cys-34. It can be anticipated from the phase of study involving bovine serum albumin that low molecular weight thiolates (reduced glutathione and N-acetylcysteine) take off Ag which are attached to proteins elsewhere in the physiological system, making these toxic metals free for toxic action.

摘要

本研究的目的是探讨牛血清白蛋白(BSA)、5,5'-二硫代双(2-硝基苯甲酸)(ESSE)、还原型谷胱甘肽、N-乙酰半胱氨酸、D-青霉胺(硫醇盐)和银金属(Ag)之间发生的交换反应。为此,通过将 264mg BSA 溶解在 5ml 反应缓冲液(pH7.8 的 0.1MKHPO)中,将 23.8mg ESSE 溶解在 1.0ml 反应缓冲液中,制备 BSA 和 Ellman 试剂的储备溶液,并将其混合在一起。通过将 0.17mg 硝酸银溶解在 1ml 反应缓冲液中,然后将 200mg BSA 溶解在相同的硝酸银溶液中,在单独的程序中制备 BSA-Ag 混合物。通过用 ESSE(85μM)和 ES(85μM)溶液处理不同稀释度的 BSA-Ag(500μM)溶液,并使用紫外-可见分光光度计记录光谱(300-450nm),确认 BSA 中 Cys-34 与 Ag 的结合。随后将(BSA-S)Ag)(典型浓度为 500μM)的色谱分离的 Ag 修饰 BSA 样品与硫醇(还原型谷胱甘肽、N-乙酰半胱氨酸和 D-青霉胺)混合。用这些低分子量硫醇处理 Ag 修饰的 BSA(典型浓度为 500μM 各),并允许反应过夜,然后进行色谱分离(Sephadex G25)。Ag 修饰的 BSA 与各种低分子量硫醇的氧化还原反应揭示了一个重要的机械现象。在还原型谷胱甘肽和 N-乙酰半胱氨酸的情况下,我们观察到相当数量的 Ellman 阴离子的快速释放,表明发生了交换,低分子量硫醇(RSH)取代了 BSA 中 Cys-34 的 Ag 物种,最终在 Cys-34 处形成二硫键(BSA-SSR)。从涉及牛血清白蛋白的研究阶段可以预期,低分子量硫醇(还原型谷胱甘肽和 N-乙酰半胱氨酸)会去除附着在生理系统中其他蛋白质上的 Ag,使这些有毒金属能够自由发挥毒性作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f89/9377917/10200ec862c1/BMRI2022-3619308.001.jpg

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