用于β-淀粉样蛋白聚集体荧光传感的 BODIPY 基化合物的合成与结构表征

IF 4 2区 化学 Q2 CHEMISTRY, PHYSICAL
Hilal Kırpık , Robert B.P. Elmes , Koray Sayin , Muhammet Kose
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引用次数: 0

摘要

阿尔茨海默病(AD)是一种与衰老相关的神经退行性疾病。根据淀粉样蛋白级联假说,β-淀粉样蛋白(Aβ)肽在大脑中聚集并堆积成 Aβ 斑块是 AD 发病的关键过程。在现有的诊断方法中,β-淀粉样蛋白(Aβ)的荧光检测因其实时检测、成本低、不受辐射、分辨率高等优点而成为阿尔茨海默病(AD)早期诊断的替代方法。在本研究中,我们设计并合成了基于 BODIPY 的化合物(BODIPY-3、BODIPY-4 和 BODIPY-5),用于 Aβ 聚集体的荧光检测。在检测 Aβ 的荧光研究中,BODIPY-5 的方酸酯单元位于 BODIPY 核心的中位,其 Kd 值为 11.7 μM,显示出良好的效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synthesis and structural characterization BODIPY-based compounds for fluorescence sensing of β-amyloid aggregates

Synthesis and structural characterization BODIPY-based compounds for fluorescence sensing of β-amyloid aggregates
Alzheimer's disease (AD) is a neurodegenerative disorder associated with aging. According to the amyloid cascade hypothesis, the aggregation and accumulation of β-amyloid (Aβ) peptides in the brain as Aβ plaques is a critical process in the pathogenesis of AD. Among the existing diagnosis methods, fluorescence detection of β-amyloid (Aβ) has emerged as an alternative method due to its advantages such as real-time detection, low cost, not exposed to radiation, and high resolution for early diagnosis of Alzheimer's disease (AD). In this study, we designed and synthesized BODIPY-based compounds (BODIPY-3, BODIPY-4 and BODIPY-5) for the fluorescence detection of Aβ aggregates. In the fluorescence studies for detecting Aβ, BODIPY-5 with the squaric acid ester unit at the meso position of the BODIPY core showed a promising effect with an 11.7 μM Kd value.
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来源期刊
Journal of Molecular Structure
Journal of Molecular Structure 化学-物理化学
CiteScore
7.10
自引率
15.80%
发文量
2384
审稿时长
45 days
期刊介绍: The Journal of Molecular Structure is dedicated to the publication of full-length articles and review papers, providing important new structural information on all types of chemical species including: • Stable and unstable molecules in all types of environments (vapour, molecular beam, liquid, solution, liquid crystal, solid state, matrix-isolated, surface-absorbed etc.) • Chemical intermediates • Molecules in excited states • Biological molecules • Polymers. The methods used may include any combination of spectroscopic and non-spectroscopic techniques, for example: • Infrared spectroscopy (mid, far, near) • Raman spectroscopy and non-linear Raman methods (CARS, etc.) • Electronic absorption spectroscopy • Optical rotatory dispersion and circular dichroism • Fluorescence and phosphorescence techniques • Electron spectroscopies (PES, XPS), EXAFS, etc. • Microwave spectroscopy • Electron diffraction • NMR and ESR spectroscopies • Mössbauer spectroscopy • X-ray crystallography • Charge Density Analyses • Computational Studies (supplementing experimental methods) We encourage publications combining theoretical and experimental approaches. The structural insights gained by the studies should be correlated with the properties, activity and/ or reactivity of the molecule under investigation and the relevance of this molecule and its implications should be discussed.
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