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An integrated digital PCR system with high universality and low cost for nucleic acid detection

Digital PCR is the most advanced PCR technology. However, due to the high price of the digital PCR analysis instrument, this powerful nucleic acid detection technology is still difficult to be popularized in the general biochemistry laboratory. Moreover, one of the biggest disadvantages of commercia...

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Autores principales: Wang, Kangning, Li, Bin, Guo, Yu, Wu, Yanqi, Li, Yan, Wu, Wenming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437218/
https://www.ncbi.nlm.nih.gov/pubmed/36061433
http://dx.doi.org/10.3389/fbioe.2022.947895
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author Wang, Kangning
Li, Bin
Guo, Yu
Wu, Yanqi
Li, Yan
Wu, Wenming
author_facet Wang, Kangning
Li, Bin
Guo, Yu
Wu, Yanqi
Li, Yan
Wu, Wenming
author_sort Wang, Kangning
collection PubMed
description Digital PCR is the most advanced PCR technology. However, due to the high price of the digital PCR analysis instrument, this powerful nucleic acid detection technology is still difficult to be popularized in the general biochemistry laboratory. Moreover, one of the biggest disadvantages of commercial digital PCR systems is the poor versatility of reagents: each instrument can only be used for a few customized kits. Herein, we built a low-cost digital PCR system. The system only relies on low-cost traditional flat-panel PCR equipment to provide temperature conditions for commercial dPCR chips, and the self-made fluorescence detection system is designed and optically optimized to meet a wide range of reagent requirements. More importantly, our system not only has a low cost (<8000 US dollars) but also has a much higher universality for nucleic acid detection reagents than the traditional commercial digital PCR system. In this study, several samples were tested. The genes used in the experiment were plasmids containing UPE-1a fragment, TP53 reference DNA, hepatitis B virus DNA, leukemia sample, SARS-COV-2 DNA, and SARS-COV-2 RNA. Under the condition that DNA can be amplified normally, the function of the dPCR system can be realized with simpler and low-price equipment. Some DNA cannot be detected by using the commercial dPCR system because of the special formula when it is configured as the reaction solution, but these DNA fluorescence signals can be clearly detected by our system, and the concentration can be calculated. Our system is more applicable than the commercial dPCR system to form a new dPCR system that is smaller and more widely applicable than commercially available machinery.
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spelling pubmed-94372182022-09-03 An integrated digital PCR system with high universality and low cost for nucleic acid detection Wang, Kangning Li, Bin Guo, Yu Wu, Yanqi Li, Yan Wu, Wenming Front Bioeng Biotechnol Bioengineering and Biotechnology Digital PCR is the most advanced PCR technology. However, due to the high price of the digital PCR analysis instrument, this powerful nucleic acid detection technology is still difficult to be popularized in the general biochemistry laboratory. Moreover, one of the biggest disadvantages of commercial digital PCR systems is the poor versatility of reagents: each instrument can only be used for a few customized kits. Herein, we built a low-cost digital PCR system. The system only relies on low-cost traditional flat-panel PCR equipment to provide temperature conditions for commercial dPCR chips, and the self-made fluorescence detection system is designed and optically optimized to meet a wide range of reagent requirements. More importantly, our system not only has a low cost (<8000 US dollars) but also has a much higher universality for nucleic acid detection reagents than the traditional commercial digital PCR system. In this study, several samples were tested. The genes used in the experiment were plasmids containing UPE-1a fragment, TP53 reference DNA, hepatitis B virus DNA, leukemia sample, SARS-COV-2 DNA, and SARS-COV-2 RNA. Under the condition that DNA can be amplified normally, the function of the dPCR system can be realized with simpler and low-price equipment. Some DNA cannot be detected by using the commercial dPCR system because of the special formula when it is configured as the reaction solution, but these DNA fluorescence signals can be clearly detected by our system, and the concentration can be calculated. Our system is more applicable than the commercial dPCR system to form a new dPCR system that is smaller and more widely applicable than commercially available machinery. Frontiers Media S.A. 2022-08-19 /pmc/articles/PMC9437218/ /pubmed/36061433 http://dx.doi.org/10.3389/fbioe.2022.947895 Text en Copyright © 2022 Wang, Li, Guo, Wu, Li and Wu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Wang, Kangning
Li, Bin
Guo, Yu
Wu, Yanqi
Li, Yan
Wu, Wenming
An integrated digital PCR system with high universality and low cost for nucleic acid detection
title An integrated digital PCR system with high universality and low cost for nucleic acid detection
title_full An integrated digital PCR system with high universality and low cost for nucleic acid detection
title_fullStr An integrated digital PCR system with high universality and low cost for nucleic acid detection
title_full_unstemmed An integrated digital PCR system with high universality and low cost for nucleic acid detection
title_short An integrated digital PCR system with high universality and low cost for nucleic acid detection
title_sort integrated digital pcr system with high universality and low cost for nucleic acid detection
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437218/
https://www.ncbi.nlm.nih.gov/pubmed/36061433
http://dx.doi.org/10.3389/fbioe.2022.947895
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