Abstract
A competitive homogeneous quenched fluorescence assay system is described for the high throughput screening of DNA conjugates that bind to single-stranded DNA. Fluorescence signal is generated by competitive binding of the sample molecule to a target strand labelled with a quencher probe, which is otherwise hybridised to a complementary strand containing a fluorescent probe. Thus fluorescence generated is related to the affinity of the sample. Competitive analysis of a number of peptide-oligonucleotide conjugates gave data that correlated well with the corresponding UV melting data. The assay will be useful for screening of large numbers of potential single-stranded binding molecules.
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CITATION STYLE
Harrison, J. G., Liu, X., & Balasubramanian, S. (1999). Screening for oligonucleotide binding affinity by a convenient fluorescence competition assay. Nucleic Acids Research, 27(17). https://doi.org/10.1093/nar/27.17.e14-i
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