Publication | Open Access
Sensitive non-radioactive dot-blot hybridization using DNA probes labelled with chelate group substituted psoralen and quantitative detection by europium ion fluorescence
52
Citations
25
References
1988
Year
EngineeringDna AnalysisMolecular BiologyChelate GroupHybridization AssaysEuropium Ion FluorescenceBioanalysisPlasmid DnaAnalytical ChemistryChromatographyBiochemistryMolecular Biological MethodOligonucleotideDna ReplicationDna ProbesNew Labelling MethodMolecular ProbesBiomolecular EngineeringNatural SciencesBiotechnologySynthetic BiologyGenetic EngineeringNucleic Acid AmplificationChemical Probe
A new labelling method for cloned DNA probes used in hybridization assays is described. The DNA insert of recombinant plasmid DNA was made partially single-stranded for the labelling reaction by a restriction enzyme digest, followed by a controlled exonuclease III incubation. A thiol-containing psoralen derivative was covalently bound through irradiation with UV-light to the remaining double-stranded region of the plasmid DNA. The psoralen-SH groups were labelled with a large number of metal chelators (diethylentriamine pentaacetic acid, DTPA) using poly-L-lysine as a macromolecular carrier. The main advantage of the labelling procedure is that a high degree of labelling is achieved without modification of the single-stranded DNA hybridizing sequences. The specific hybrids were labelled after filter hybridization with europium ions through the chelating groups of DTPA. The europium ions were quantitatively detected by time-resolved fluorometry. The sensitivity of the assay for target DNA detection was in the low picogram range, comparable to radioactively labelled DNA probes.
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