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A unified sensor architecture for isothermal detection of double-stranded DNA, oligonucleotides, and small molecules.


ABSTRACT: Pathogen detection is an important problem in many areas of medicine and agriculture, which can involve genomic or transcriptomic signatures or small-molecule metabolites. We report a unified, DNA-based sensor architecture capable of isothermal detection of double-stranded DNA targets, single-stranded oligonucleotides, and small molecules. Each sensor contains independent target detection and reporter modules, enabling rapid design. We detected gene variants on plasmids by using a straightforward isothermal denaturation protocol. The sensors were highly specific, even with a randomized DNA background. We achieved a limit of detection of ?15 pM for single-stranded targets and ?5 nM for targets on denatured plasmids. By incorporating a blocked aptamer sequence, we also detected small molecules using the same sensor architecture. This work provides a starting point for multiplexed detection of multi-strain pathogens, and disease states caused by genetic variants (e.g., sickle cell anemia).

SUBMITTER: Brown CW 

PROVIDER: S-EPMC4422402 | biostudies-literature | 2015 Mar

REPOSITORIES: biostudies-literature

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A unified sensor architecture for isothermal detection of double-stranded DNA, oligonucleotides, and small molecules.

Brown Carl W CW   Lakin Matthew R MR   Fabry-Wood Aurora A   Horwitz Eli K EK   Baker Nicholas A NA   Stefanovic Darko D   Graves Steven W SW  

Chembiochem : a European journal of chemical biology 20150206 5


Pathogen detection is an important problem in many areas of medicine and agriculture, which can involve genomic or transcriptomic signatures or small-molecule metabolites. We report a unified, DNA-based sensor architecture capable of isothermal detection of double-stranded DNA targets, single-stranded oligonucleotides, and small molecules. Each sensor contains independent target detection and reporter modules, enabling rapid design. We detected gene variants on plasmids by using a straightforwar  ...[more]

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