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High-throughput extraction on a dynamic solid phase for low-abundance biomarker isolation from biological samples
Liquid biopsy, in particular circulating tumor DNA (ctDNA) analysis, has paved the way for a new noninvasive approach to cancer diagnosis, treatment selection and follow-up. As a crucial step in the analysis, the extraction of the genetic material from a complex matrix needs to meet specific require...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10480215/ https://www.ncbi.nlm.nih.gov/pubmed/37680311 http://dx.doi.org/10.1038/s41378-023-00582-4 |
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author | Alexandre, Lucile Araya-Farias, Monica Nguyen, Manh-Louis Naoumi, Nikoletta Gropplero, Giacomo Gizeli, Electra Malaquin, Laurent Descroix, Stéphanie |
author_facet | Alexandre, Lucile Araya-Farias, Monica Nguyen, Manh-Louis Naoumi, Nikoletta Gropplero, Giacomo Gizeli, Electra Malaquin, Laurent Descroix, Stéphanie |
author_sort | Alexandre, Lucile |
collection | PubMed |
description | Liquid biopsy, in particular circulating tumor DNA (ctDNA) analysis, has paved the way for a new noninvasive approach to cancer diagnosis, treatment selection and follow-up. As a crucial step in the analysis, the extraction of the genetic material from a complex matrix needs to meet specific requirements such as high specificity and low loss of target. Here, we developed a new generation of microfluidic fluidized beds (FBs) that enable the efficient extraction and preconcentration of specific ctDNA sequences from human serum with flow rates up to 15 µL/min. We first demonstrated that implementation of a vibration system inducing flow rate fluctuations combined with a mixture of different bead sizes significantly enhanced bead homogeneity, thereby increasing capture efficiency. Taking advantage of this new generation of high-throughput magnetic FBs, we then developed a new method to selectively capture a double-stranded (dsDNA) BRAF mutated DNA sequence in complex matrices such as patient serum. Finally, as proof of concept, ligation chain reaction (LCR) assays were performed to specifically amplify a mutated BRAF sequence, allowing the detection of concentrations as low as 6 × 10(4) copies/µL of the mutated DNA sequence in serum. [Image: see text] |
format | Online Article Text |
id | pubmed-10480215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104802152023-09-07 High-throughput extraction on a dynamic solid phase for low-abundance biomarker isolation from biological samples Alexandre, Lucile Araya-Farias, Monica Nguyen, Manh-Louis Naoumi, Nikoletta Gropplero, Giacomo Gizeli, Electra Malaquin, Laurent Descroix, Stéphanie Microsyst Nanoeng Article Liquid biopsy, in particular circulating tumor DNA (ctDNA) analysis, has paved the way for a new noninvasive approach to cancer diagnosis, treatment selection and follow-up. As a crucial step in the analysis, the extraction of the genetic material from a complex matrix needs to meet specific requirements such as high specificity and low loss of target. Here, we developed a new generation of microfluidic fluidized beds (FBs) that enable the efficient extraction and preconcentration of specific ctDNA sequences from human serum with flow rates up to 15 µL/min. We first demonstrated that implementation of a vibration system inducing flow rate fluctuations combined with a mixture of different bead sizes significantly enhanced bead homogeneity, thereby increasing capture efficiency. Taking advantage of this new generation of high-throughput magnetic FBs, we then developed a new method to selectively capture a double-stranded (dsDNA) BRAF mutated DNA sequence in complex matrices such as patient serum. Finally, as proof of concept, ligation chain reaction (LCR) assays were performed to specifically amplify a mutated BRAF sequence, allowing the detection of concentrations as low as 6 × 10(4) copies/µL of the mutated DNA sequence in serum. [Image: see text] Nature Publishing Group UK 2023-09-06 /pmc/articles/PMC10480215/ /pubmed/37680311 http://dx.doi.org/10.1038/s41378-023-00582-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Alexandre, Lucile Araya-Farias, Monica Nguyen, Manh-Louis Naoumi, Nikoletta Gropplero, Giacomo Gizeli, Electra Malaquin, Laurent Descroix, Stéphanie High-throughput extraction on a dynamic solid phase for low-abundance biomarker isolation from biological samples |
title | High-throughput extraction on a dynamic solid phase for low-abundance biomarker isolation from biological samples |
title_full | High-throughput extraction on a dynamic solid phase for low-abundance biomarker isolation from biological samples |
title_fullStr | High-throughput extraction on a dynamic solid phase for low-abundance biomarker isolation from biological samples |
title_full_unstemmed | High-throughput extraction on a dynamic solid phase for low-abundance biomarker isolation from biological samples |
title_short | High-throughput extraction on a dynamic solid phase for low-abundance biomarker isolation from biological samples |
title_sort | high-throughput extraction on a dynamic solid phase for low-abundance biomarker isolation from biological samples |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10480215/ https://www.ncbi.nlm.nih.gov/pubmed/37680311 http://dx.doi.org/10.1038/s41378-023-00582-4 |
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