Guangxi Scientific Research Centre of Traditional Chinese Medicine, Guangxi University of Chinese Medicine, Nanning 530200, PR China; Guangxi Key Laboratory of Chinese Medicine Foundation Research, Guangxi University of Chinese Medicine, Nanning 530200, PR China.
Guangxi Scientific Research Centre of Traditional Chinese Medicine, Guangxi University of Chinese Medicine, Nanning 530200, PR China; Guangxi Key Laboratory of Chinese Medicine Foundation Research, Guangxi University of Chinese Medicine, Nanning 530200, PR China.
Talanta. 2017 Aug 1;170:350-357. doi: 10.1016/j.talanta.2017.04.021. Epub 2017 Apr 14.
A sensitive and stable bioassay for the detection of Aβ oligomer (Aβo), a potentially promising candidate biomarker for Alzheimer's disease (AD) diagnosis, was developed using FeO magnetic nanoparticles (MNPs) as the recognition and concentration elements and BaYF:Yb,Er upconversion nanoparticles (UCNPs) as highly sensitive labels, conjugated with the Aβo aptamer (DNA1) and the complementary oligonucleotide of the Aβo aptamer (DNA2), respectively. The DNA1 hybridized with DNA2 to form the duplex structure on the surface of the MNPs/UCNPs nanocomposites probe. When the target Aβo was introduced, the aptamer DNA1 preferentially bound with Aβo and caused the dissociation of some complementary DNA2, liberating some UCNP-labeled complementary DNA2 and leading to a decreased upconversion fluorescent intensity on the surface of MNPs. The decreased fluorescence intensity of UCNPs was related to the concentration of Aβo in the range of 0.2-15nM with a detection limit of 36 pM. The developed method then was successfully applied to measure Aβo in artificial cerebrospinal fluid. Benefiting from the magnetic separation and concentration effect of MNPs, the high sensitivity of UCNPs, as well as the selectivity and stability of the aptamer, the present strategy offered valuable information related to early diagnosis of AD process.
开发了一种灵敏且稳定的生物测定法,用于检测 Aβ 寡聚物(Aβo),Aβo 是阿尔茨海默病(AD)诊断有前途的候选生物标志物。该方法使用 FeO 磁性纳米颗粒(MNPs)作为识别和浓缩元素,BaYF:Yb,Er 上转换纳米颗粒(UCNPs)作为高度灵敏的标记物,分别与 Aβo 适体(DNA1)和 Aβo 适体的互补寡核苷酸(DNA2)结合。DNA1 与 DNA2 杂交,在 MNPs/UCNPs 纳米复合材料探针表面形成双链结构。当引入靶标 Aβo 时,适体 DNA1 优先与 Aβo 结合,导致一些互补 DNA2 解离,释放一些 UCNP 标记的互补 DNA2,导致 MNPs 表面上的上转换荧光强度降低。UCNP 的荧光强度降低与 Aβo 的浓度在 0.2-15nM 范围内相关,检测限为 36 pM。该方法随后成功应用于人工脑脊液中 Aβo 的测量。受益于 MNPs 的磁分离和浓缩效应、UCNPs 的高灵敏度以及适体的选择性和稳定性,该策略提供了与 AD 进程早期诊断相关的有价值的信息。