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Holographic molecular binding assays

We demonstrate that holographic particle characterization can directly detect binding of proteins to functionalized colloidal probe particles by monitoring the associated change in the particles’ size. This label-free molecular binding assay uses in-line holographic video microscopy to measure the d...

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Detalles Bibliográficos
Autores principales: Zagzag, Yvonne, Soddu, M. Francesca, Hollingsworth, Andrew D., Grier, David G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005168/
https://www.ncbi.nlm.nih.gov/pubmed/32029807
http://dx.doi.org/10.1038/s41598-020-58833-7
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author Zagzag, Yvonne
Soddu, M. Francesca
Hollingsworth, Andrew D.
Grier, David G.
author_facet Zagzag, Yvonne
Soddu, M. Francesca
Hollingsworth, Andrew D.
Grier, David G.
author_sort Zagzag, Yvonne
collection PubMed
description We demonstrate that holographic particle characterization can directly detect binding of proteins to functionalized colloidal probe particles by monitoring the associated change in the particles’ size. This label-free molecular binding assay uses in-line holographic video microscopy to measure the diameter and refractive index of individual probe spheres as they flow down a microfluidic channel. Pooling measurements on 10(4) particles yields the population-average diameter with an uncertainty smaller than 0.5 nm, which is sufficient to detect sub-monolayer coverage by bound proteins. We demonstrate this method by monitoring binding of NeutrAvidin to biotinylated spheres and binding of immunoglobulin G to spheres functionalized with protein A.
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spelling pubmed-70051682020-02-18 Holographic molecular binding assays Zagzag, Yvonne Soddu, M. Francesca Hollingsworth, Andrew D. Grier, David G. Sci Rep Article We demonstrate that holographic particle characterization can directly detect binding of proteins to functionalized colloidal probe particles by monitoring the associated change in the particles’ size. This label-free molecular binding assay uses in-line holographic video microscopy to measure the diameter and refractive index of individual probe spheres as they flow down a microfluidic channel. Pooling measurements on 10(4) particles yields the population-average diameter with an uncertainty smaller than 0.5 nm, which is sufficient to detect sub-monolayer coverage by bound proteins. We demonstrate this method by monitoring binding of NeutrAvidin to biotinylated spheres and binding of immunoglobulin G to spheres functionalized with protein A. Nature Publishing Group UK 2020-02-06 /pmc/articles/PMC7005168/ /pubmed/32029807 http://dx.doi.org/10.1038/s41598-020-58833-7 Text en © The Author(s) 2020 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/.
spellingShingle Article
Zagzag, Yvonne
Soddu, M. Francesca
Hollingsworth, Andrew D.
Grier, David G.
Holographic molecular binding assays
title Holographic molecular binding assays
title_full Holographic molecular binding assays
title_fullStr Holographic molecular binding assays
title_full_unstemmed Holographic molecular binding assays
title_short Holographic molecular binding assays
title_sort holographic molecular binding assays
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005168/
https://www.ncbi.nlm.nih.gov/pubmed/32029807
http://dx.doi.org/10.1038/s41598-020-58833-7
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