Abstract
We describe a novel assay for detection of point mutations. The method combines the specificity and sensitivity of the polymerase chain reaction (PCR) and allele-specific oligonucleotides (ASO) with highly sensitive time-resolved fluorometry. ASO probes differing by a single base substitution and labeled with europium (Eu) chelates were hybridized in solution simultaneously with a biotinylated oligomer to a PCR-amplified nucleic acid fragment. The hybrids formed were then collected onto streptavidincoated microtitration wells. Subsequently, the hybrids were washed under stringent conditions and the remaining ASO probe was measured in a time-resolved fluorometer. We discuss the strategy underlying the design of the Eu-labeled ASO probes for the solution hybridization assay. The method was applied to the detection of the Z-mutation in the α1-antitrypsin gene. Evaluation of whole-blood samples spotted on Guthrie cards demonstrated successful accuracy of the method.
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CITATION STYLE
Dahlén, P., Carlson, J., Liukkonen, L., Lilja, H., Siitari, H., Hurskainen, P., … Lövgren, T. (1993). Europium-labeled oligonucleotides to detect point mutations: application to PI Z α1-antitrypsin deficiency. Clinical Chemistry, 39(8), 1626–1631. https://doi.org/10.1093/clinchem/39.8.1626
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