2009
DOI: 10.1080/00032710903137384
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Hybridization Study of PNA-DNA in the Solution and Surface-Solution Interface for Biosensor Application

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Cited by 3 publications
(4 citation statements)
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“…These results demonstrated that the hybridization between PNA and the DNA was not dependent on FAM functionalization. Several hybridization studies in solution have demonstrated that PNA/complementary ON recognition takes place by Watson–Crick base pairing, that is, A-T and G-C base pairing [ 3 , 46 , 47 , 48 , 49 ]. Therefore, no specific recognition could occur between the synthesized PNA and the non-complementary DNA polyT sequence in solution.…”
Section: Resultsmentioning
confidence: 99%
“…These results demonstrated that the hybridization between PNA and the DNA was not dependent on FAM functionalization. Several hybridization studies in solution have demonstrated that PNA/complementary ON recognition takes place by Watson–Crick base pairing, that is, A-T and G-C base pairing [ 3 , 46 , 47 , 48 , 49 ]. Therefore, no specific recognition could occur between the synthesized PNA and the non-complementary DNA polyT sequence in solution.…”
Section: Resultsmentioning
confidence: 99%
“…These results demonstrated that the hybridization between PNA and the DNA was not dependent on FAM functionalization. Several hybridization studies in solution have demonstrated that PNA/complementary ON recognition takes place by Watson-Crick base pairing, that is, A-T and G-C base pairing [3,[45][46][47][48]. Therefore, no specific recognition could occur between the synthesized PNA and the non-complementary DNA polyT sequence in solution.…”
Section: Resultsmentioning
confidence: 99%
“…PNAs have shown to retain their efficient hybridization properties in solution after attachment to the surfaces of substrates. PNA probes can hybridize with DNA targets in buffers with low ionic strength, which can lower the possibility of forming DNA secondary or tertiary structures. Under physiological conditions, the PNA–DNA duplexes have higher melting temperatures than corresponding DNA–DNA duplexes by approximately 1.5 °C per base pair . In addition, unlike DNA probes that can only detect single-stranded nucleic acid targets, PNA-based probes can bind to double-stranded DNA, which makes it possible to achieve direct detection of clinical specimens.…”
Section: Introductionmentioning
confidence: 99%
“…Under physiological conditions, the PNA− DNA duplexes have higher melting temperatures than corresponding DNA−DNA duplexes by approximately 1.5 °C per base pair. 17 In addition, unlike DNA probes that can only detect single-stranded nucleic acid targets, PNA-based probes can bind to double-stranded DNA, 18−22 which makes it possible to achieve direct detection of clinical specimens. In fact, analysis of relatively small arrays of PNA oligomers have demonstrate their potential as excellent alternatives to DNA microarrays.…”
Section: ■ Introductionmentioning
confidence: 99%