| Literature DB >> 32475109 |
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
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Year: 2020 PMID: 32475109 PMCID: PMC7872156 DOI: 10.1021/acssensors.0c00052
Source DB: PubMed Journal: ACS Sens ISSN: 2379-3694 Impact factor: 7.711