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基于膜转移的酶修饰金纳米颗粒比色法DNA检测

[Membrane transfer-based colorimetric DNA detection using enzyme modified gold nanoparticles].

作者信息

Li Haiyan, Jing Fengxiang, Gao Qiuyue, Jia Chunping, Chen Jiwu, Jin Qinghui, Zhao Jianlong

机构信息

School of Life Science, East China Normal University, Shanghai 200062, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2010 Aug;26(8):1135-42.

Abstract

We report here a novel membrane transfer-based DNA detection method, in which alkaline phosphatase labeled gold nanoparticle (AuNP) probes were used as a means to amplify the detection signal. In this method, the capture probe P1, complimentary to the 3' end of target DNA, was immobilized on the chip. The multi-component AuNP probes were prepared by co-coating AuNPs with the detecting probe P2, complimentary to the 5' end of target DNA, and two biotin-labeled signal probes (T10 and T40) with different lengths. In the presence of target DNA, DNA hybridization led to the attachment of AuNPs on the chip surface where specific DNA sequences were located in a "sandwich" format. Alkaline phosphatase was then introduced to the surface via biotine-streptavidin interaction. By using BCIP/NBT alkaline phosphatase color development kit, a colorimetric DNA detection was achieved through membrane transfer. The signal on the membrane was then detected by the naked eye or an ordinary optical scanner. The method provided a detection of limit of 1 pmol/L for synthesized target DNA and 0.23 pmol/L for PCR products of Mycobacterium tuberculosis 16S rDNA when the ratio of probes used was 9:1:1 (T10:T40:P2). The method described here has many desirable advantages including high sensitivity, simple operation, and no need of sophisticated equipment. The method can be potentially used for reliable biosensings.

摘要

我们在此报告一种基于膜转移的新型DNA检测方法,其中碱性磷酸酶标记的金纳米颗粒(AuNP)探针被用作放大检测信号的手段。在该方法中,与靶DNA 3'端互补的捕获探针P1固定在芯片上。通过将金纳米颗粒与与靶DNA 5'端互补的检测探针P2以及两种不同长度的生物素标记信号探针(T10和T40)共同包被来制备多组分金纳米颗粒探针。在存在靶DNA的情况下,DNA杂交导致金纳米颗粒以“三明治”形式附着在芯片表面特定DNA序列所在的位置。然后通过生物素-链霉亲和素相互作用将碱性磷酸酶引入表面。通过使用BCIP/NBT碱性磷酸酶显色试剂盒,通过膜转移实现了比色法DNA检测。然后用肉眼或普通光学扫描仪检测膜上的信号。当所用探针比例为9:1:1(T10:T40:P2)时,该方法对合成靶DNA的检测限为1 pmol/L,对结核分枝杆菌16S rDNA的PCR产物的检测限为0.23 pmol/L。这里描述的方法具有许多理想的优点,包括高灵敏度、操作简单且无需复杂设备。该方法有可能用于可靠的生物传感。

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