Literature DB >> 32475109

Nucleic Acid Quantitation with Log-Linear Response Hybridization Probe Sets.

Lucia R Wu1, John Z Fang1, Dmitriy Khodakov1, David Yu Zhang1,2.   

Abstract

Concentrations of different nucleic acid species in biological samples span many orders of magnitude. A real-time polymerase chain reaction maps the concentration of a target nucleic acid sequence log-linearly into cycle threshold to enable quantitation with a wide dynamic range but suffers from enzymatic biases. Here, we present a general design for constructing hybridization probe sets with highly log-linear response curves to enable accurate enzyme-free quantitation across large ranges (more than 6 logs) of target DNA concentrations. The sensitivity of each component probe is accurately adjusted via formulation stoichiometry to reduce the standard error of target quantitation down to 7%. As a proof of concept, we show multiplexed quantitation of three microRNA species in total RNA of the human brain and liver.

Entities:  

Keywords:  RNA quantitation; dynamic range; enzyme-free biosensor; nucleic acid hybridization; nucleic acids thermodynamics; toehold probe

Mesh:

Substances:

Year:  2020        PMID: 32475109      PMCID: PMC7872156          DOI: 10.1021/acssensors.0c00052

Source DB:  PubMed          Journal:  ACS Sens        ISSN: 2379-3694            Impact factor:   7.711


  30 in total

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Review 8.  Oligonucleotide-based label-free detection with optical microresonators: strategies and challenges.

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9.  Optimizing the specificity of nucleic acid hybridization.

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Journal:  Nat Chem       Date:  2012-01-22       Impact factor: 24.427

10.  Real-Time and Selective Detection of Single Nucleotide DNA Mutations Using Surface Engineered Microtoroids.

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2.  Development of a Pharmacogenetic Lab-on-Chip Assay Based on the In-Check Technology to Screen for Genetic Variations Associated to Adverse Drug Reactions to Common Chemotherapeutic Agents.

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