TY - JOUR
T1 - Target-assembled ExciProbes: Application to DNA detection at the level of PCR product and plasmid DNA
AU - Walsh, Lindsey
AU - Gbaj, Abdul
AU - Savage, Hannah E.
AU - Bacigalupo, M. Candelaria Rogert
AU - Bichenkova, Elena V.
AU - Douglas, Kenneth T.
PY - 2007/12
Y1 - 2007/12
N2 - Recently, we introduced a novel exciplex-based approach for detection of nucleic acids using a model DNA-mounted exciplex system, consisting of two 8-mer ExciProbes hybridized to a complementary 16-mer DNA target. We now show, for the first time, that this approach can be used to detect DNA at the level of PCR product and plasmid, when the target sequence (5′-GCCAAACACAGAATCG- 3′) was embedded in long DNA molecules (PCR products and ∼3 Kbp plasmid). A remarkably stringent demand is made of the solvent conditions for this exciplex emission to occur, viz., emission is optimal for DNA at 80% trifluoroethanol, even in the plasmid situations, raising the question of the molecular structural basis of this system. We show that a perfectly matched plasmid target can be differentiated from target containing single nucleotide substitutions; hence, ExciProbes could be applied to SNP analysis. The effect of counter cations (Na+, K+, and Mg2+) and PCR additives on exciplex emission has been also examined. ©Adenine Press (2007).
AB - Recently, we introduced a novel exciplex-based approach for detection of nucleic acids using a model DNA-mounted exciplex system, consisting of two 8-mer ExciProbes hybridized to a complementary 16-mer DNA target. We now show, for the first time, that this approach can be used to detect DNA at the level of PCR product and plasmid, when the target sequence (5′-GCCAAACACAGAATCG- 3′) was embedded in long DNA molecules (PCR products and ∼3 Kbp plasmid). A remarkably stringent demand is made of the solvent conditions for this exciplex emission to occur, viz., emission is optimal for DNA at 80% trifluoroethanol, even in the plasmid situations, raising the question of the molecular structural basis of this system. We show that a perfectly matched plasmid target can be differentiated from target containing single nucleotide substitutions; hence, ExciProbes could be applied to SNP analysis. The effect of counter cations (Na+, K+, and Mg2+) and PCR additives on exciplex emission has been also examined. ©Adenine Press (2007).
U2 - DOI:10.1080/07391102.2007.10507171
DO - DOI:10.1080/07391102.2007.10507171
M3 - Article
SN - 0739-1102
VL - 25
SP - 219
EP - 229
JO - Journal of Biomolecular Structure and Dynamics
JF - Journal of Biomolecular Structure and Dynamics
IS - 3
ER -