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Integration of Magnetic Bead-Based Cell Selection into Complex Isolations
[Image: see text] Magnetic bead-based analyte capture has emerged as a ubiquitous method in cell isolation, enabling the highly specific capture of target populations through simple magnetic manipulation. To date, no “one-size fits all” magnetic bead has been widely adopted leading to an overwhelmin...
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/PMC5928489/ https://www.ncbi.nlm.nih.gov/pubmed/29732449 http://dx.doi.org/10.1021/acsomega.7b01427 |
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author | Pezzi, Hannah M. Niles, David J. Schehr, Jennifer L. Beebe, David J. Lang, Joshua M. |
author_facet | Pezzi, Hannah M. Niles, David J. Schehr, Jennifer L. Beebe, David J. Lang, Joshua M. |
author_sort | Pezzi, Hannah M. |
collection | PubMed |
description | [Image: see text] Magnetic bead-based analyte capture has emerged as a ubiquitous method in cell isolation, enabling the highly specific capture of target populations through simple magnetic manipulation. To date, no “one-size fits all” magnetic bead has been widely adopted leading to an overwhelming number of commercial beads. Ultimately, the ideal bead is one that not only facilitates cell isolation but also proves compatible with the widest range of downstream applications and analytic endpoints. Despite the diverse offering of sizes, coatings, and conjugation chemistries, few studies exist to benchmark the performance characteristics of different commercially available beads; importantly, these bead characteristics ultimately determine the ability of a bead to integrate into the user’s assay. In this report, we evaluate bead-based cell isolation considerations, approaches, and results across a subset of commercially available magnetic beads (Dynabeads FlowComps, Dynabeads CELLection, GE Healthcare Sera-Mag SpeedBeads streptavidin-blocked magnetic particles, Dynabeads M-270s, Dynabeads M-280s) to compare and contrast both capture-specific traits (i.e., purity, capture efficacy, and contaminant isolations) and endpoint compatibility (i.e., protein localization, fluorescence imaging, and nucleic acid extraction). We identify specific advantages and contexts of use in which distinct bead products may facilitate experimental goals and integrate into downstream applications. |
format | Online Article Text |
id | pubmed-5928489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American
Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-59284892018-05-02 Integration of Magnetic Bead-Based Cell Selection into Complex Isolations Pezzi, Hannah M. Niles, David J. Schehr, Jennifer L. Beebe, David J. Lang, Joshua M. ACS Omega [Image: see text] Magnetic bead-based analyte capture has emerged as a ubiquitous method in cell isolation, enabling the highly specific capture of target populations through simple magnetic manipulation. To date, no “one-size fits all” magnetic bead has been widely adopted leading to an overwhelming number of commercial beads. Ultimately, the ideal bead is one that not only facilitates cell isolation but also proves compatible with the widest range of downstream applications and analytic endpoints. Despite the diverse offering of sizes, coatings, and conjugation chemistries, few studies exist to benchmark the performance characteristics of different commercially available beads; importantly, these bead characteristics ultimately determine the ability of a bead to integrate into the user’s assay. In this report, we evaluate bead-based cell isolation considerations, approaches, and results across a subset of commercially available magnetic beads (Dynabeads FlowComps, Dynabeads CELLection, GE Healthcare Sera-Mag SpeedBeads streptavidin-blocked magnetic particles, Dynabeads M-270s, Dynabeads M-280s) to compare and contrast both capture-specific traits (i.e., purity, capture efficacy, and contaminant isolations) and endpoint compatibility (i.e., protein localization, fluorescence imaging, and nucleic acid extraction). We identify specific advantages and contexts of use in which distinct bead products may facilitate experimental goals and integrate into downstream applications. American Chemical Society 2018-04-06 /pmc/articles/PMC5928489/ /pubmed/29732449 http://dx.doi.org/10.1021/acsomega.7b01427 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Pezzi, Hannah M. Niles, David J. Schehr, Jennifer L. Beebe, David J. Lang, Joshua M. Integration of Magnetic Bead-Based Cell Selection into Complex Isolations |
title | Integration of Magnetic Bead-Based Cell Selection
into Complex Isolations |
title_full | Integration of Magnetic Bead-Based Cell Selection
into Complex Isolations |
title_fullStr | Integration of Magnetic Bead-Based Cell Selection
into Complex Isolations |
title_full_unstemmed | Integration of Magnetic Bead-Based Cell Selection
into Complex Isolations |
title_short | Integration of Magnetic Bead-Based Cell Selection
into Complex Isolations |
title_sort | integration of magnetic bead-based cell selection
into complex isolations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5928489/ https://www.ncbi.nlm.nih.gov/pubmed/29732449 http://dx.doi.org/10.1021/acsomega.7b01427 |
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