Hairpin Probe for Sequence-specific Recognition of Double-stranded DNA on Simian Virus 40 |
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Authors: | ZHANG Hong ZOU Li LI Ruimin ZHAO Mingqin LING Liansheng |
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Affiliation: | 1. School of Chemistry, Sun Yat-sen University, Guangzhou 510275, P. R. China; 2. College of Tobacco Science, Henan Agricultural University, Zhengzhou 450000, P. R. China |
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Abstract: | Simian virus 40(SV40) is a polyomavirus and can induce a series of different tumors. The recognition of SV40 genome is crucial to tumor diagnosis and gene therapy. Herein, a sensitive and selective colorimetric method for sequence-specific recognition of homopyrimidine·homopurine duplex DNA(dsDNA) of SV40(4424—4440, gp6) was established with a hairpin probe based upon the formation of triplex DNA. Hairpin probe 5'-CCC TAC CCA TTT TTT CTT CTC TTT CCT GGG TAG GGC GGG TTG GG-3'(HP) containing G-rich sequence and 17-bp triplex-forming sequence was used as the signal probe, which was stem-loop structure alone and exhibited low catalytic activity. Upon its binding to the target duplex of SV40, hairpin probe transferred from stem-loop structure to parallel triplex DNA, accompanied by the recovery of catalytic activity of DNAzyme and a sharp increase of absorbance. Under optimum conditions, the absorbance was increased proportionally to the concentration of dsDNA over the range from 500 pmol/L to 40.0 nmol/L with a detection limit of 433 pmol/L. Moreover, satisfied results were obtained when the assay was used to recognize the mismatched sequences. |
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Keywords: | Simian virus 40 Hairpin probe Triplex DNA G-Quadruplex DNAzyme |
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