ArticleBiomolecular detection and quantification2019
Challenging the proposed causes of the PCR plateau phase.
Article in Biomolecular detection and quantification, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.
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Who cites it
14 citing papers in PubMed.
- A Multiplex PCR-Based Assay for Authentication of Six Commercially Important Cephalopod Species.Foods (Basel, Switzerland) · 2026Article
- Implementing L-DNA analogs as mirrors of PCR reactant hybridization state: theoretical and practical guidelines for PCR cycle control.Analytical methods : advancing methods and applications · 2024Article
- A practical workflow for forensic species identification using direct sequencing of real-time PCR products.Molecular biology reports · 2023Article
- Visual diagnosis of COVID-19 disease based on serum metabolites using a paper-based electronic tongue.Analytica chimica acta · 2022Article
- A colorimetric electronic tongue for point-of-care detection of COVID-19 using salivary metabolites.Talanta · 2022Article
- Non-invasive detection of COVID-19 using a microfluidic-based colorimetric sensor array sensitive to urinary metabolites.Mikrochimica acta · 2022Article
- Optimized quantitative PCR analysis of random DNA aptamer libraries.Analytical biochemistry · 2022Article
- Isothermal Amplification with a Target-Mimicking Internal Control and Quantitative Lateral Flow Readout for Rapid HIV Viral Load Testing in Low-Resource Settings.Analytical chemistry · 2022Article
- An advanced and efficient asymmetric PCR method for microarray applications.Frontiers in bioengineering and biotechnology · 2022Article
- Comparison of Real-Q 2019-nCoV and DaAn Gene 2019-nCoV polymerase chain reaction assays for the detection of SARS-CoV-2.Journal of clinical laboratory analysis · 2022Article
- Loop-Mediated Isothermal Amplification (LAMP) as a Promising Point-of-Care Diagnostic Strategy in Avian Virus Research.Animals : an open access journal from MDPI · 2021Review
- Molecular Survey and Genetic Diversity ofMicroorganisms · 2021Article
- Affine analysis for quantitative PCR measurements.Analytical and bioanalytical chemistry · 2020Article
- A Single-Tube HNB-Based Loop-Mediated Isothermal Amplification for the Robust Detection of theInternational journal of molecular sciences · 2020Article
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2 authors.
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Abstract
Despite the wide-spread use of the polymerase chain reaction (PCR) in various life-science applications, the causes of arrested amplicon generation in late cycles have not been confidently identified. This so-called plateau phase has been attributed to depletion or thermal break-down of primers or nucleotides, thermal inactivation of the DNA polymerase, and product accumulation resulting in competition between primer annealing and product re-hybridization as well as blocking of DNA polymerase by double-stranded amplicons. In the current study, we experimentally investigate the proposed limiting factors of PCR product formation. By applying robust and validated qPCR assays, we elucidate the impact of adding non-target and target amplicons to the reactions, mimicking the high amount of products in late PCR cycles. Further, the impact of increased primer concentrations and thermal stability of reagents are explored. Our results show that high amounts of non-target amplicons inhibit amplification by binding to the DNA polymerase, but that this effect is counteracted by addition of more DNA polymerase or prolonged annealing/extension times. Adding high amounts of target amplicons that also act as templates in the reaction is far less inhibitory to amplification, although a decrease in amplification rate is seen. When primer concentrations are increased, both amplification rates and end-product yields are elevated. Taken together, our results suggest that the main cause of PCR plateau formation is primer depletion and not product accumulation or degradation of reagents. We stress that a PCR plateau caused by primer depletion is assay-dependent, i.e. dependent on the primer design and primer characteristics such as the probability of primer-dimer formation. Our findings contribute to an improved understanding of the major parameters controlling the PCR dynamics at later cycles and the limitations of continued product formation, which in the end can facilitate PCR optimization.
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