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MassCode Liquid Arrays as a Tool for Multiplexed High-Throughput Genetic Profiling
Multiplexed detection assays that analyze a modest number of nucleic acid targets over large sample sets are emerging as the preferred testing approach in such applications as routine pathogen typing, outbreak monitoring, and diagnostics. However, very few DNA testing platforms have proven to offer...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3081317/ https://www.ncbi.nlm.nih.gov/pubmed/21544191 http://dx.doi.org/10.1371/journal.pone.0018967 |
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author | Richmond, Gregory S. Khine, Htet Zhou, Tina T. Ryan, Daniel E. Brand, Tony McBride, Mary T. Killeen, Kevin |
author_facet | Richmond, Gregory S. Khine, Htet Zhou, Tina T. Ryan, Daniel E. Brand, Tony McBride, Mary T. Killeen, Kevin |
author_sort | Richmond, Gregory S. |
collection | PubMed |
description | Multiplexed detection assays that analyze a modest number of nucleic acid targets over large sample sets are emerging as the preferred testing approach in such applications as routine pathogen typing, outbreak monitoring, and diagnostics. However, very few DNA testing platforms have proven to offer a solution for mid-plexed analysis that is high-throughput, sensitive, and with a low cost per test. In this work, an enhanced genotyping method based on MassCode technology was devised and integrated as part of a high-throughput mid-plexing analytical system that facilitates robust qualitative differential detection of DNA targets. Samples are first analyzed using MassCode PCR (MC-PCR) performed with an array of primer sets encoded with unique mass tags. Lambda exonuclease and an array of MassCode probes are then contacted with MC-PCR products for further interrogation and target sequences are specifically identified. Primer and probe hybridizations occur in homogeneous solution, a clear advantage over micro- or nanoparticle suspension arrays. The two cognate tags coupled to resultant MassCode hybrids are detected in an automated process using a benchtop single quadrupole mass spectrometer. The prospective value of using MassCode probe arrays for multiplexed bioanalysis was demonstrated after developing a 14plex proof of concept assay designed to subtype a select panel of Salmonella enterica serogroups and serovars. This MassCode system is very flexible and test panels can be customized to include more, less, or different markers. |
format | Text |
id | pubmed-3081317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30813172011-05-04 MassCode Liquid Arrays as a Tool for Multiplexed High-Throughput Genetic Profiling Richmond, Gregory S. Khine, Htet Zhou, Tina T. Ryan, Daniel E. Brand, Tony McBride, Mary T. Killeen, Kevin PLoS One Research Article Multiplexed detection assays that analyze a modest number of nucleic acid targets over large sample sets are emerging as the preferred testing approach in such applications as routine pathogen typing, outbreak monitoring, and diagnostics. However, very few DNA testing platforms have proven to offer a solution for mid-plexed analysis that is high-throughput, sensitive, and with a low cost per test. In this work, an enhanced genotyping method based on MassCode technology was devised and integrated as part of a high-throughput mid-plexing analytical system that facilitates robust qualitative differential detection of DNA targets. Samples are first analyzed using MassCode PCR (MC-PCR) performed with an array of primer sets encoded with unique mass tags. Lambda exonuclease and an array of MassCode probes are then contacted with MC-PCR products for further interrogation and target sequences are specifically identified. Primer and probe hybridizations occur in homogeneous solution, a clear advantage over micro- or nanoparticle suspension arrays. The two cognate tags coupled to resultant MassCode hybrids are detected in an automated process using a benchtop single quadrupole mass spectrometer. The prospective value of using MassCode probe arrays for multiplexed bioanalysis was demonstrated after developing a 14plex proof of concept assay designed to subtype a select panel of Salmonella enterica serogroups and serovars. This MassCode system is very flexible and test panels can be customized to include more, less, or different markers. Public Library of Science 2011-04-22 /pmc/articles/PMC3081317/ /pubmed/21544191 http://dx.doi.org/10.1371/journal.pone.0018967 Text en Richmond et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Richmond, Gregory S. Khine, Htet Zhou, Tina T. Ryan, Daniel E. Brand, Tony McBride, Mary T. Killeen, Kevin MassCode Liquid Arrays as a Tool for Multiplexed High-Throughput Genetic Profiling |
title | MassCode Liquid Arrays as a Tool for Multiplexed High-Throughput Genetic Profiling |
title_full | MassCode Liquid Arrays as a Tool for Multiplexed High-Throughput Genetic Profiling |
title_fullStr | MassCode Liquid Arrays as a Tool for Multiplexed High-Throughput Genetic Profiling |
title_full_unstemmed | MassCode Liquid Arrays as a Tool for Multiplexed High-Throughput Genetic Profiling |
title_short | MassCode Liquid Arrays as a Tool for Multiplexed High-Throughput Genetic Profiling |
title_sort | masscode liquid arrays as a tool for multiplexed high-throughput genetic profiling |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3081317/ https://www.ncbi.nlm.nih.gov/pubmed/21544191 http://dx.doi.org/10.1371/journal.pone.0018967 |
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