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Single-Molecule enzyme-linked immunosorbent assay detects serum proteins at subfemtomolar concentrations

The detection of single protein molecules1,2 in blood could help identify many new diagnostic protein markers. We report an approach for detecting hundreds to thousands of individual protein molecules simultaneously that enables the detection of very low concentrations of proteins. Proteins are capt...

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Detalles Bibliográficos
Autores principales: Rissin, David M., Kan, Cheuk W., Campbell, Todd G., Howes, Stuart C., Fournier, David R., Song, Linan, Piech, Tomasz, Patel, Purvish P., Chang, Lei, Rivnak, Andrew J., Ferrell, Evan P., Randall, Jeffrey D., Provuncher, Gail K., Walt, David R., Duffy, David C.
Formato: Texto
Lenguaje:English
Publicado: 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2919230/
https://www.ncbi.nlm.nih.gov/pubmed/20495550
http://dx.doi.org/10.1038/nbt.1641
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author Rissin, David M.
Kan, Cheuk W.
Campbell, Todd G.
Howes, Stuart C.
Fournier, David R.
Song, Linan
Piech, Tomasz
Patel, Purvish P.
Chang, Lei
Rivnak, Andrew J.
Ferrell, Evan P.
Randall, Jeffrey D.
Provuncher, Gail K.
Walt, David R.
Duffy, David C.
author_facet Rissin, David M.
Kan, Cheuk W.
Campbell, Todd G.
Howes, Stuart C.
Fournier, David R.
Song, Linan
Piech, Tomasz
Patel, Purvish P.
Chang, Lei
Rivnak, Andrew J.
Ferrell, Evan P.
Randall, Jeffrey D.
Provuncher, Gail K.
Walt, David R.
Duffy, David C.
author_sort Rissin, David M.
collection PubMed
description The detection of single protein molecules1,2 in blood could help identify many new diagnostic protein markers. We report an approach for detecting hundreds to thousands of individual protein molecules simultaneously that enables the detection of very low concentrations of proteins. Proteins are captured on microscopic beads and labeled with an enzyme, such that each bead has either one or zero enzyme-labeled proteins. By isolating these beads in arrays of 50-femtoliter reaction chambers, single proteins can be detected by fluorescence imaging. By singulating molecules in these arrays, ~10–20 enzymes can be detected in 100 μL (~10(−19) M). Single molecule enzyme-linked immunosorbent assays (digital ELISA) based on singulation of enzyme labels enabled the detection of clinically-relevant proteins in serum at concentrations (<10(−15) M) much lower than conventional ELISA3-5. Digital ELISA detected prostate specific antigen in all tested sera from patients who had undergone radical prostatectomy, down to 14 fg/mL (0.4 fM).
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spelling pubmed-29192302010-12-01 Single-Molecule enzyme-linked immunosorbent assay detects serum proteins at subfemtomolar concentrations Rissin, David M. Kan, Cheuk W. Campbell, Todd G. Howes, Stuart C. Fournier, David R. Song, Linan Piech, Tomasz Patel, Purvish P. Chang, Lei Rivnak, Andrew J. Ferrell, Evan P. Randall, Jeffrey D. Provuncher, Gail K. Walt, David R. Duffy, David C. Nat Biotechnol Article The detection of single protein molecules1,2 in blood could help identify many new diagnostic protein markers. We report an approach for detecting hundreds to thousands of individual protein molecules simultaneously that enables the detection of very low concentrations of proteins. Proteins are captured on microscopic beads and labeled with an enzyme, such that each bead has either one or zero enzyme-labeled proteins. By isolating these beads in arrays of 50-femtoliter reaction chambers, single proteins can be detected by fluorescence imaging. By singulating molecules in these arrays, ~10–20 enzymes can be detected in 100 μL (~10(−19) M). Single molecule enzyme-linked immunosorbent assays (digital ELISA) based on singulation of enzyme labels enabled the detection of clinically-relevant proteins in serum at concentrations (<10(−15) M) much lower than conventional ELISA3-5. Digital ELISA detected prostate specific antigen in all tested sera from patients who had undergone radical prostatectomy, down to 14 fg/mL (0.4 fM). 2010-05-23 2010-06 /pmc/articles/PMC2919230/ /pubmed/20495550 http://dx.doi.org/10.1038/nbt.1641 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Rissin, David M.
Kan, Cheuk W.
Campbell, Todd G.
Howes, Stuart C.
Fournier, David R.
Song, Linan
Piech, Tomasz
Patel, Purvish P.
Chang, Lei
Rivnak, Andrew J.
Ferrell, Evan P.
Randall, Jeffrey D.
Provuncher, Gail K.
Walt, David R.
Duffy, David C.
Single-Molecule enzyme-linked immunosorbent assay detects serum proteins at subfemtomolar concentrations
title Single-Molecule enzyme-linked immunosorbent assay detects serum proteins at subfemtomolar concentrations
title_full Single-Molecule enzyme-linked immunosorbent assay detects serum proteins at subfemtomolar concentrations
title_fullStr Single-Molecule enzyme-linked immunosorbent assay detects serum proteins at subfemtomolar concentrations
title_full_unstemmed Single-Molecule enzyme-linked immunosorbent assay detects serum proteins at subfemtomolar concentrations
title_short Single-Molecule enzyme-linked immunosorbent assay detects serum proteins at subfemtomolar concentrations
title_sort single-molecule enzyme-linked immunosorbent assay detects serum proteins at subfemtomolar concentrations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2919230/
https://www.ncbi.nlm.nih.gov/pubmed/20495550
http://dx.doi.org/10.1038/nbt.1641
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