Abstract:Target double-stranded DNA (dsDNA) or single-stranded DNA (ssDNA) can activate the trans-cleavage activity of the CRISPR/Cas12a, cutting the surrounding non-target ssDNA arbitrarily. In typical CRISPR/Cas12a system, this non-target ssDNA with...
“…The uorescence of 2-AP is highly quenched by base-stacking interaction with natural bases in DNA oligonucleotides, making it an extraordinarily sensitive uorescent probe for nucleic acid structure and biosensors. [22][23][24] Several mechanisms have been proposed for the quenching effect of 2-AP, mainly focusing on photoinduced electron transfer with neighboring bases. [25][26][27][28] The phenomenon of 2-AP quenching has been used to study mispair recognition, base ipping, local melting, protein binding, and electron and energy transfer.…”
Reversible structural changes in DNA nanomachines have great potential in the field of bioanalysis. Here, we demonstrate an assembly strategy for quencher-free and tunable DNA tweezers based on 2-aminopurine (2-AP),...
“…The uorescence of 2-AP is highly quenched by base-stacking interaction with natural bases in DNA oligonucleotides, making it an extraordinarily sensitive uorescent probe for nucleic acid structure and biosensors. [22][23][24] Several mechanisms have been proposed for the quenching effect of 2-AP, mainly focusing on photoinduced electron transfer with neighboring bases. [25][26][27][28] The phenomenon of 2-AP quenching has been used to study mispair recognition, base ipping, local melting, protein binding, and electron and energy transfer.…”
Reversible structural changes in DNA nanomachines have great potential in the field of bioanalysis. Here, we demonstrate an assembly strategy for quencher-free and tunable DNA tweezers based on 2-aminopurine (2-AP),...
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