Membrane transfer-based colorimetric DNA detection using enzyme modified gold nanoparticles.
- Author:
Haiyan LI
1
;
Fengxiang JING
;
Qiuyue GAO
;
Chunping JIA
;
Jiwu CHEN
;
Qinghui JIN
;
Jianlong ZHAO
Author Information
1. School of Life Science, East China Normal University, Shanghai 200062, China.
- Publication Type:Journal Article
- MeSH:
Colorimetry;
methods;
DNA Probes;
chemistry;
genetics;
DNA, Bacterial;
genetics;
Gold;
chemistry;
Humans;
Metal Nanoparticles;
chemistry;
Mycobacterium tuberculosis;
isolation & purification;
Nucleic Acid Hybridization;
methods;
Oligonucleotide Array Sequence Analysis;
methods
- From:
Chinese Journal of Biotechnology
2010;26(8):1135-1142
- CountryChina
- Language:Chinese
-
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.
