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聚 A 尾和荧光标记的适体-金纳米粒子缀合物,用于碘化物诱导配体置换的荧光开启生物测定。

PolyA-tailed and fluorophore-labeled aptamer-gold nanoparticle conjugate for fluorescence turn-on bioassay using iodide-induced ligand displacement.

机构信息

State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, Jiangsu, China.

State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, Jiangsu, China.

出版信息

Biosens Bioelectron. 2015 Apr 15;66:43-9. doi: 10.1016/j.bios.2014.10.047. Epub 2014 Oct 23.

DOI:10.1016/j.bios.2014.10.047
PMID:25460880
Abstract

Depending on the strong affinity of polyA sequence to gold (or silver) surface, applicability of polyA-tailed DNA-gold (or silver) nanoparticle conjugates in homogeneous and heterogeneous protein assays was first demonstrated. Interestingly, when using polyA-tailed, fluophore-labeled DNA-AuNP conjugate, it was found that iodide and thiosulfate anions could act as the ligand displacing reagent to detach polyA-tailed DNA strands from AuNP surface and simultaneously activate the AuNP-quenched fluorophores by destroying the polyA-AuNP interaction via a divide-and-conquer strategy. Based on this new discovery, we have developed a novel, cost-effective and sandwich-type fluorescence turn-on aptasensor for highly sensitive and specific thrombin detection, what took advantage of aptamer-conjugated magnetic beads (apt-MBs) for protein capture and separation, and iodide-induced fluorescence recovery of activatable polyA-based AuNP probes through ligand displacement for fluorescence turn-on detection. This proposed aptasensor could detect thrombin specifically with a detection limit as low as 89pM, which was better than or comparable to many existing fluorescent thrombin assays. Importantly, employment of such polyA-based AuNP conjugate not only avoids the use of thiolated oligonucleotides and thiol-containing displacing reagents, but also offers new possibilities for fabricating convenient and cost-effective bioanalytical applications.

摘要

基于聚 A 序列与金(或银)表面的强亲和力,首次证明了聚 A 尾 DNA-金(或银)纳米粒子缀合物在均相和非均相蛋白质分析中的适用性。有趣的是,当使用聚 A 尾、荧光标记的 DNA-AuNP 缀合物时,发现碘化物和硫代硫酸盐阴离子可以作为配体置换试剂,从 AuNP 表面上分离出聚 A 尾 DNA 链,并通过分而治之的策略破坏聚 A-AuNP 相互作用,同时激活 AuNP 猝灭荧光团。基于这一新发现,我们开发了一种新颖、经济高效的三明治型荧光开启适体传感器,用于高灵敏度和特异性凝血酶检测,该传感器利用与适配体偶联的磁性珠(apt-MBs)进行蛋白质捕获和分离,以及通过配体置换诱导激活的基于聚 A 的 AuNP 探针的荧光恢复来进行荧光开启检测。该适体传感器可以特异性地检测凝血酶,检测限低至 89pM,优于或可与许多现有的荧光凝血酶检测相媲美。重要的是,这种基于聚 A 的 AuNP 缀合物的应用不仅避免了使用巯基化寡核苷酸和含巯基的置换试剂,还为制造方便、经济高效的生物分析应用提供了新的可能性。

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