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Next-Generation Digital Polymerase Chain Reaction: High-Dynamic-Range Single-Molecule DNA Counting via Ultrapartitioning
[Image: see text] Digital PCR (dPCR) was first conceived for single-molecule quantitation. However, current dPCR systems often require DNA templates to share partitions due to limited partitioning capacities. Here, we introduce UltraPCR, a next-generation dPCR system where DNA counting is performed...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9798378/ https://www.ncbi.nlm.nih.gov/pubmed/36508568 http://dx.doi.org/10.1021/acs.analchem.2c03649 |
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author | Shum, Eleen Y. Lai, Janice H. Li, Sixing Lee, Haeun G. Soliman, Jesse Raol, Vedant K. Lee, Cavina K. Fodor, Stephen P.A. Fan, H. Christina |
author_facet | Shum, Eleen Y. Lai, Janice H. Li, Sixing Lee, Haeun G. Soliman, Jesse Raol, Vedant K. Lee, Cavina K. Fodor, Stephen P.A. Fan, H. Christina |
author_sort | Shum, Eleen Y. |
collection | PubMed |
description | [Image: see text] Digital PCR (dPCR) was first conceived for single-molecule quantitation. However, current dPCR systems often require DNA templates to share partitions due to limited partitioning capacities. Here, we introduce UltraPCR, a next-generation dPCR system where DNA counting is performed in a single-molecule regimen through a 6-log dynamic range using a swift and parallelized workflow. Each UltraPCR reaction is divided into >30 million partitions without microfluidics to achieve single template occupancy. Combined with a unique emulsion chemistry, partitions are optically clear, enabling the use of a three-dimensional imaging technique to rapidly detect DNA-positive partitions. Single-molecule occupancy also allows for more straightforward multiplex assay development due to the absence of partition-specific competition. As a proof of concept, we developed a 222-plex UltraPCR assay and demonstrated its potential use as a rapid, low-cost screening assay for noninvasive prenatal testing for as low as 4% trisomy fraction samples with high precision, accuracy, and reproducibility. |
format | Online Article Text |
id | pubmed-9798378 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-97983782022-12-30 Next-Generation Digital Polymerase Chain Reaction: High-Dynamic-Range Single-Molecule DNA Counting via Ultrapartitioning Shum, Eleen Y. Lai, Janice H. Li, Sixing Lee, Haeun G. Soliman, Jesse Raol, Vedant K. Lee, Cavina K. Fodor, Stephen P.A. Fan, H. Christina Anal Chem [Image: see text] Digital PCR (dPCR) was first conceived for single-molecule quantitation. However, current dPCR systems often require DNA templates to share partitions due to limited partitioning capacities. Here, we introduce UltraPCR, a next-generation dPCR system where DNA counting is performed in a single-molecule regimen through a 6-log dynamic range using a swift and parallelized workflow. Each UltraPCR reaction is divided into >30 million partitions without microfluidics to achieve single template occupancy. Combined with a unique emulsion chemistry, partitions are optically clear, enabling the use of a three-dimensional imaging technique to rapidly detect DNA-positive partitions. Single-molecule occupancy also allows for more straightforward multiplex assay development due to the absence of partition-specific competition. As a proof of concept, we developed a 222-plex UltraPCR assay and demonstrated its potential use as a rapid, low-cost screening assay for noninvasive prenatal testing for as low as 4% trisomy fraction samples with high precision, accuracy, and reproducibility. American Chemical Society 2022-12-12 2022-12-27 /pmc/articles/PMC9798378/ /pubmed/36508568 http://dx.doi.org/10.1021/acs.analchem.2c03649 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Shum, Eleen Y. Lai, Janice H. Li, Sixing Lee, Haeun G. Soliman, Jesse Raol, Vedant K. Lee, Cavina K. Fodor, Stephen P.A. Fan, H. Christina Next-Generation Digital Polymerase Chain Reaction: High-Dynamic-Range Single-Molecule DNA Counting via Ultrapartitioning |
title | Next-Generation
Digital Polymerase Chain Reaction:
High-Dynamic-Range Single-Molecule DNA Counting via Ultrapartitioning |
title_full | Next-Generation
Digital Polymerase Chain Reaction:
High-Dynamic-Range Single-Molecule DNA Counting via Ultrapartitioning |
title_fullStr | Next-Generation
Digital Polymerase Chain Reaction:
High-Dynamic-Range Single-Molecule DNA Counting via Ultrapartitioning |
title_full_unstemmed | Next-Generation
Digital Polymerase Chain Reaction:
High-Dynamic-Range Single-Molecule DNA Counting via Ultrapartitioning |
title_short | Next-Generation
Digital Polymerase Chain Reaction:
High-Dynamic-Range Single-Molecule DNA Counting via Ultrapartitioning |
title_sort | next-generation
digital polymerase chain reaction:
high-dynamic-range single-molecule dna counting via ultrapartitioning |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9798378/ https://www.ncbi.nlm.nih.gov/pubmed/36508568 http://dx.doi.org/10.1021/acs.analchem.2c03649 |
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