A novel viscosity sensitive hemicyanine fluorescent dye for real-time imaging of amyloid-β aggregation

IF 6 2区 医学 Q1 CHEMISTRY, MEDICINAL
Wenjing Wang , Zhenzhuo Mo , Lu Han, Huijie Zuo, Yalu Chen, Yafei Fang, Xiang Li, Kai Wang, Jie Pan
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Abstract

Alzheimer's Disease (AD) is a neurodegenerative disease, of which β-amyloid (Aβ) deposition is one of the most important pathological features. It has been reported that during Aβ aggregation, the microenvironment around the Aβ protein is altered in terms of viscosity and polarity. In this work, we developed five novel hemicyanine fluorescent probes (MZs). After screening the photochemical properties, MZ-2 and 3 were found to enable the rapid detection of Aβ42 aggregates, which were also sensitive to ambient viscosity. After comparison the structure of probes, we also observed that extensions of conjugated π-systems effectively cause redshifts of excitation wavelength. In the meanwhile, hydroxyl groups with weaker ionization strengths are more responsive to Aβ42 aggregates than sulfonate groups, probably due to the small size of the hydroxyl group and the acidity. Overall, MZ-2 showed the best response to Aβ42 aggregates (15.35-fold) and viscosity (17.6-fold). MZ-2 can quickly cross the blood-brain barrier (BBB), enabling high-fidelity imaging of Aβ42 aggregates in the mice brain.

Abstract Image

Abstract Image

用于淀粉样蛋白-β聚集实时成像的新型粘度敏感半氰基荧光染料
阿尔茨海默病(AD)是一种神经退行性疾病,β淀粉样蛋白(Aβ)沉积是其最重要的病理特征之一。据报道,在 Aβ 聚集过程中,Aβ 蛋白周围的微环境在粘度和极性方面发生了改变。在这项工作中,我们开发了五种新型半氰基荧光探针(MZs)。经过光化学特性筛选,我们发现 MZ-2 和 3 能够快速检测 Aβ42 聚集体,而且对环境粘度也很敏感。在对探针的结构进行比较后,我们还观察到共轭 π 系统的扩展有效地导致了激发波长的红移。同时,与磺酸盐基团相比,电离强度较弱的羟基对 Aβ42 聚合体的反应更灵敏,这可能是由于羟基的小尺寸和酸性所致。总体而言,MZ-2 对 Aβ42 聚集体(15.35 倍)和粘度(17.6 倍)的反应最好。MZ-2能快速穿过血脑屏障(BBB),从而对小鼠大脑中的Aβ42聚集体进行高保真成像。
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来源期刊
CiteScore
11.70
自引率
9.00%
发文量
863
审稿时长
29 days
期刊介绍: The European Journal of Medicinal Chemistry is a global journal that publishes studies on all aspects of medicinal chemistry. It provides a medium for publication of original papers and also welcomes critical review papers. A typical paper would report on the organic synthesis, characterization and pharmacological evaluation of compounds. Other topics of interest are drug design, QSAR, molecular modeling, drug-receptor interactions, molecular aspects of drug metabolism, prodrug synthesis and drug targeting. The journal expects manuscripts to present the rational for a study, provide insight into the design of compounds or understanding of mechanism, or clarify the targets.
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