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Real-Time, Digital LAMP with Commercial Microfluidic Chips Reveals the Interplay of Efficiency, Speed, and Background Amplification as a Function of Reaction Temperature and Time
[Image: see text] Real-time, isothermal, digital nucleic acid amplification is emerging as an attractive approach for a multitude of applications including diagnostics, mechanistic studies, and assay optimization. Unfortunately, there is no commercially available and affordable real-time, digital in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6322147/ https://www.ncbi.nlm.nih.gov/pubmed/30565936 http://dx.doi.org/10.1021/acs.analchem.8b04324 |
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author | Rolando, Justin C. Jue, Erik Schoepp, Nathan G. Ismagilov, Rustem F. |
author_facet | Rolando, Justin C. Jue, Erik Schoepp, Nathan G. Ismagilov, Rustem F. |
author_sort | Rolando, Justin C. |
collection | PubMed |
description | [Image: see text] Real-time, isothermal, digital nucleic acid amplification is emerging as an attractive approach for a multitude of applications including diagnostics, mechanistic studies, and assay optimization. Unfortunately, there is no commercially available and affordable real-time, digital instrument validated for isothermal amplification; thus, most researchers have not been able to apply digital, real-time approaches to isothermal amplification. Here, we generate an approach to real-time digital loop-mediated isothermal amplification (LAMP) using commercially available microfluidic chips and reagents and open-source components. We demonstrate this approach by testing variables that influence LAMP reaction speed and the probability of detection. By analyzing the interplay of amplification efficiency, background, and speed of amplification, this real-time digital method enabled us to test enzymatic performance over a range of temperatures, generating high-precision kinetic and end-point measurements. We were able to identify the unique optimal temperature for two polymerase enzymes while accounting for amplification efficiency, nonspecific background, and time to threshold. We validated this digital LAMP assay and pipeline by performing a phenotypic antibiotic susceptibility test on 17 archived clinical urine samples from patients diagnosed with urinary tract infections. We provide all the necessary workflows to perform digital LAMP using standard laboratory equipment and commercially available materials. This real-time digital approach will be useful to others in the future to understand the fundamentals of isothermal chemistries, including which components determine amplification fate, reaction speed, and enzymatic performance. Researchers can also adapt this pipeline, which uses only standard equipment and commercial components, to quickly study and optimize assays using precise, real-time digital quantification, accelerating development of critically needed diagnostics. |
format | Online Article Text |
id | pubmed-6322147 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-63221472019-01-09 Real-Time, Digital LAMP with Commercial Microfluidic Chips Reveals the Interplay of Efficiency, Speed, and Background Amplification as a Function of Reaction Temperature and Time Rolando, Justin C. Jue, Erik Schoepp, Nathan G. Ismagilov, Rustem F. Anal Chem [Image: see text] Real-time, isothermal, digital nucleic acid amplification is emerging as an attractive approach for a multitude of applications including diagnostics, mechanistic studies, and assay optimization. Unfortunately, there is no commercially available and affordable real-time, digital instrument validated for isothermal amplification; thus, most researchers have not been able to apply digital, real-time approaches to isothermal amplification. Here, we generate an approach to real-time digital loop-mediated isothermal amplification (LAMP) using commercially available microfluidic chips and reagents and open-source components. We demonstrate this approach by testing variables that influence LAMP reaction speed and the probability of detection. By analyzing the interplay of amplification efficiency, background, and speed of amplification, this real-time digital method enabled us to test enzymatic performance over a range of temperatures, generating high-precision kinetic and end-point measurements. We were able to identify the unique optimal temperature for two polymerase enzymes while accounting for amplification efficiency, nonspecific background, and time to threshold. We validated this digital LAMP assay and pipeline by performing a phenotypic antibiotic susceptibility test on 17 archived clinical urine samples from patients diagnosed with urinary tract infections. We provide all the necessary workflows to perform digital LAMP using standard laboratory equipment and commercially available materials. This real-time digital approach will be useful to others in the future to understand the fundamentals of isothermal chemistries, including which components determine amplification fate, reaction speed, and enzymatic performance. Researchers can also adapt this pipeline, which uses only standard equipment and commercial components, to quickly study and optimize assays using precise, real-time digital quantification, accelerating development of critically needed diagnostics. American Chemical Society 2018-12-19 2019-01-02 /pmc/articles/PMC6322147/ /pubmed/30565936 http://dx.doi.org/10.1021/acs.analchem.8b04324 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Rolando, Justin C. Jue, Erik Schoepp, Nathan G. Ismagilov, Rustem F. Real-Time, Digital LAMP with Commercial Microfluidic Chips Reveals the Interplay of Efficiency, Speed, and Background Amplification as a Function of Reaction Temperature and Time |
title | Real-Time, Digital LAMP with Commercial Microfluidic
Chips Reveals the Interplay of Efficiency, Speed, and Background Amplification
as a Function of Reaction Temperature and Time |
title_full | Real-Time, Digital LAMP with Commercial Microfluidic
Chips Reveals the Interplay of Efficiency, Speed, and Background Amplification
as a Function of Reaction Temperature and Time |
title_fullStr | Real-Time, Digital LAMP with Commercial Microfluidic
Chips Reveals the Interplay of Efficiency, Speed, and Background Amplification
as a Function of Reaction Temperature and Time |
title_full_unstemmed | Real-Time, Digital LAMP with Commercial Microfluidic
Chips Reveals the Interplay of Efficiency, Speed, and Background Amplification
as a Function of Reaction Temperature and Time |
title_short | Real-Time, Digital LAMP with Commercial Microfluidic
Chips Reveals the Interplay of Efficiency, Speed, and Background Amplification
as a Function of Reaction Temperature and Time |
title_sort | real-time, digital lamp with commercial microfluidic
chips reveals the interplay of efficiency, speed, and background amplification
as a function of reaction temperature and time |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6322147/ https://www.ncbi.nlm.nih.gov/pubmed/30565936 http://dx.doi.org/10.1021/acs.analchem.8b04324 |
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