太赫兹光谱分析从人血清白蛋白中提取的淀粉样蛋白纤维

Shakirah Wahida Shamsul Bahri, Siti Nor Khadijah Addis, Nur Farizan Munajat, Nabilah Kasim, Hidayatul Aini Zakaria
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引用次数: 0

摘要

淀粉样纤维又称蛋白质纤维,是蛋白质的不规则集合体,呈交叉β构型。太赫兹辐射是电磁波谱中 0.3 到 10 太赫兹(THz)的一个部分,由于淀粉样蛋白纤维呈圆柱形,因此可以与它们相互作用。本研究的目的是探索太赫兹光谱作为一种非侵入性手段检测蛋白质纤维逐渐生长的潜力。在这项研究中,人工诱导人血清白蛋白(HSA)形成蛋白质纤维。通过荧光光谱、傅立叶变换红外(FTIR)光谱、紫外可见光谱和太赫兹时域光谱(THz-TDS)确认了纤维的形成。为了启动这一过程,先将浓度为 160 µM 的 HSA 溶于蒸馏水中,然后在两种样品中加入 60% 的乙醇进行稀释。对于含铜(II)的储备溶液,HSA 与铜(II)的比例保持为 1:1(160 µM)。随后,每组样品在 65 °C 下加热 6 小时以培养纤维,然后在室温下分别保存 30 天、60 天和 90 天后再进行评估。人血清白蛋白孵育产生的淀粉样纤维由 ThT 荧光证明,傅立叶变换红外光谱显示纤维出现在酰胺 I 波段内,从 1630 cm-¹ 延伸到 1650 cm-¹,紫外可见光谱显示蛋白质纤维吸光度在孵育期间增加。太赫兹光谱吸光度随着蛋白质纤维的加热时间延长而逐渐升高,这是由于蛋白质纤维周围存在水合壳。通过这些光谱方法,阐明了纤化过程导致β-片状结构和无序螺旋结构的逐渐发展,以及太赫兹光谱作为检测和监测淀粉样变性疾病的非侵入性工具的潜力,有望为早期诊断和治疗策略带来启示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Terahertz Spectroscopy Analysis of Amyloid Fibrils Derived from Human Serum Albumin
Amyloid fibrils, also referred to as protein fibrils, represent irregular assemblies of proteins exhibiting a cross-β configuration. Terahertz radiation, a segment of the electromagnetic spectrum spanning 0.3 to 10 terahertz (THz), is known to interact with these fibrils due to their cylindrical shape. This study's objective was to explore the potential of terahertz spectroscopy as a non-invasive means to detect the progressive growth of protein fibrils. In this investigation, human serum albumin (HSA) was synthetically induced to form protein fibrils. Confirmation of fibril formation was done by fluorescence spectroscopy, Fourier transform infrared (FTIR) spectroscopy, UV-Vis spectroscopy, and Terahertz time-domain spectroscopy (THz-TDS). To initiate the process, HSA was dissolved in distilled water at a concentration of 160 µM, followed by the addition of 60% ethanol to both samples for dilution. The HSA to Cu (II) ratio was maintained at 1:1 (160 µM) for stock solutions containing Cu (II). Subsequently, each set underwent a 6-hour heating phase at 65 °C to cultivate fibrils, which were then stored at room temperature for 30, 60, and 90 days before evaluation. Incubation of human serum albumin yielded amyloid fibrils as evidenced by ThT fluorescence, FT-IR spectroscopy revealed an emergence of fibrils within the amide I bands, extending from 1630 cm⁻¹ to 1650 cm⁻¹ and UV-Vis spectroscopy disclosed the augmentation of protein fibril absorbance over the incubation period. THz spectroscopy absorbance progressively heightened with prolonged heating of the protein fibrils due to the hydration shell surrounding them. Through these spectroscopic methods, it was elucidated that the fibrillation process led to the gradual development of β-sheet and unordered helix structures as well as the potential of THz spectroscopy as non-invasive tool for detection and monitoring of amyloidal diseases, promising insights into early diagnosis and treatment strategies.
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