Nucleic Acids Research, Vol 25, Issue 20 4139-4146, Copyright © 1997 by Oxford University Press
AH Uddin, PA Piunno, RH Hudson, MJ Damha and UJ Krull
A fiber optic biosensor was used for the fluorimetric detection of T/AT
triple-helical DNA formation. The surfaces of two sets of fused silica
optical fibers were functionalized with hexaethylene oxide linkers from
which decaadenylic acid oligonucleotides were grown in the 3'to 5'and 5'to
3'direction, respectively, using a DNA synthesizer. Fluorescence studies of
hybridization showed unequivocal hybridization between oligomers
immobilized on the fibers and complementary oligonucleotides from the
solution phase, as detected by fluorescence from intercalated ethidium
bromide. The complementary oligonucleotide, dT10, which was expected to
Watson-Crick hybridize upon cooling the system below the duplex melting
temperature ( T m), provided a fluorescence intensity with a negative
temperature coefficient. Upon further cooling, to the point where the
pyrimidine motif T*AT triple-helix formation occurred, a fluorescence
intensity change with a positive temperature coefficient was observed. The
reverse-Hoogsteen T.AT triplex, which is known to form with branched
nucleic acids, provided a corresponding decrease in fluorescence intensity
with decreasing temperature. Full analytical signal evolution was
attainable in minutes.
ARTICLES
A fiber optic biosensor for fluorimetric detection of triple-helical DNA
Department of Chemistry, Otto Maas Chemistry Building, McGill University, Montreal, Quebec H3A 2K6, Canada.
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