Key Laboratory of New Optoelectronic Functional Materials (Henan Province), College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang, Henan 455000, People's Republic of China.
Key Laboratory of New Optoelectronic Functional Materials (Henan Province), College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang, Henan 455000, People's Republic of China.
Biosens Bioelectron. 2016 Nov 15;85:625-632. doi: 10.1016/j.bios.2016.05.066. Epub 2016 May 24.
Beta-amyloid (Aβ) peptides are the major constituents of senile plaques in the brains of Alzheimer's disease (AD) patients. Aβ monomers (AβMs) can coalesce to form small, soluble oligomers (AβOs), followed by reorganization and assembly into long, thread-like fibrils (AβFs). Recently, soluble AβOs have been regarded as reliable molecular biomarkers for the diagnosis of AD because of their high toxicity for neuronal synapse and high concentration levels in the brains of AD patients. In this work, we reported a label-free, sensitive and selective method for visual and fluorescent detection of AβOs based on the inner filter effect (IFE) of gold nanoparticles (AuNPs) on the fluorescence of CdTe quantum dots (QDs). Specifically, the fluorescence of CdTe QDs was quenched significantly by AuNPs through the IFE. PrP(95-110), an AβOs-specific binding peptide from cellular prion protein, triggered the aggregation and color change of AuNPs suspension; thus, the IFE of AuNPs on the fluorescence of CdTe QDs was weakened and the fluorescence intensity was recovered. However, in the presence of AβOs, the specific interaction of AβOs and PrP(95-110) prevented the absorption of PrP(95-110) onto the surface of AuNPs. As a result, the aggregation of AuNPs was inhibited and the fluorescence intensity of CdTe QDs was quenched again. This label-free method is specific for detection of AβOs but not for AβMs and AβFs. The detection limits were found to be 0.5nM for the visual assay and 0.2nM for the fluorescent detection. We believe that this work would be valuable for many investigations related to AD diagnosis and drug discovery.
β-淀粉样蛋白(Aβ)肽是阿尔茨海默病(AD)患者大脑中老年斑的主要成分。Aβ单体(AβMs)可以凝聚形成小的、可溶性寡聚物(AβOs),然后重组并组装成长而细的纤维(AβFs)。最近,由于可溶性 AβOs 对神经元突触具有高毒性且在 AD 患者大脑中的浓度水平较高,因此被认为是 AD 诊断的可靠分子生物标志物。在这项工作中,我们报道了一种基于金纳米粒子(AuNPs)对碲化镉量子点(CdTe QDs)荧光的内滤效应(IFE)的无标记、敏感和选择性检测 AβOs 的方法。具体来说,通过 IFE,AuNPs 显著猝灭了 CdTe QDs 的荧光。PrP(95-110)是细胞朊病毒蛋白中的一种 AβOs 特异性结合肽,引发了 AuNPs 悬浮液的聚集和颜色变化;因此,AuNPs 对 CdTe QDs 荧光的 IFE 减弱,荧光强度恢复。然而,在存在 AβOs 的情况下,AβOs 与 PrP(95-110)的特异性相互作用阻止了 PrP(95-110)吸附到 AuNPs 表面。结果,AuNPs 的聚集受到抑制,CdTe QDs 的荧光强度再次猝灭。这种无标记方法特异性检测 AβOs,但不检测 AβMs 和 AβFs。目视检测的检测限为 0.5nM,荧光检测的检测限为 0.2nM。我们相信这项工作对于许多与 AD 诊断和药物发现相关的研究将具有重要价值。