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基于银纳米颗粒的DNA杂交和单核苷酸多态性的超灵敏化学发光检测

Silver nanoparticle-based ultrasensitive chemiluminescent detection of DNA hybridization and single-nucleotide polymorphisms.

作者信息

Liu Cheng-Hui, Li Zheng-Ping, Du Bao-An, Duan Xin-Rui, Wang Yu-Cong

机构信息

College of Chemistry and Environment Science, Hebei University, Baoding 071002, China.

出版信息

Anal Chem. 2006 Jun 1;78(11):3738-44. doi: 10.1021/ac0522409.

Abstract

A new nanoparticle-based chemiluminescent (CL) method has been developed for the ultrasensitive detection of DNA hybridization. The assay relies on a sandwich-type DNA hybridization in which the DNA targets are first hybridized to the captured oligonucleotide probes immobilized on polystyrene microwells and then the silver nanoparticles modified with alkylthiol-capped oligonucleotides are used as probes to monitor the presence of the specific target DNA. After being anchored on the hybrids, silver nanoparticles are dissolved to Ag+ in HNO3 solution and sensitively determined by a coupling CL reaction system (Ag+-Mn2+-K2S2O8-H3PO4-luminol). The combination of the remarkable sensitivity of the CL method with the large number of Ag+ released from each hybrid allows the detection of specific sequence DNA targets at levels as low as 5 fM. The sensitivity increases 6 orders of magnitude greater than that of the gold nanoparticle-based colorimetric method and is comparable to that of surface-enhanced Raman spectroscopy, which is one of the most sensitive detection approaches available to the nanoparticle-based detection for DNA hybridization. Moreover, the perfectly complementary DNA targets and the single-base mismatched DNA strands can be evidently differentiated through controlling the temperature, which indicates that the proposed CL assay offers great promise for single-nucleotide polymorphism analysis.

摘要

一种基于纳米粒子的新型化学发光(CL)方法已被开发用于超灵敏检测DNA杂交。该检测方法依赖于夹心型DNA杂交,其中DNA靶标首先与固定在聚苯乙烯微孔上的捕获寡核苷酸探针杂交,然后将用烷基硫醇封端的寡核苷酸修饰的银纳米颗粒用作探针来监测特定靶标DNA的存在。银纳米颗粒锚定在杂交体上后,在硝酸溶液中溶解为Ag+,并通过耦合CL反应体系(Ag+-Mn2+-K2S2O8-H3PO4-鲁米诺)进行灵敏测定。CL方法的显著灵敏度与每个杂交体释放的大量Ag+相结合,使得能够检测低至5 fM水平的特定序列DNA靶标。其灵敏度比基于金纳米颗粒的比色法提高了6个数量级,与表面增强拉曼光谱法相当,表面增强拉曼光谱法是基于纳米颗粒的DNA杂交检测中最灵敏的检测方法之一。此外,通过控制温度可以明显区分完全互补的DNA靶标和单碱基错配的DNA链,这表明所提出的CL检测方法在单核苷酸多态性分析方面具有巨大潜力。

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