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µFBI: A Microfluidic Bead-Based Immunoassay for Multiplexed Detection of Proteins from a µL Sample Volume

BACKGROUND: Over the last ten years, miniaturized multiplexed immunoassays have become robust, reliable research tools that enable researchers to simultaneously determine a multitude of parameters. Among the numerous analytical protein arrays available, bead-based assay systems have evolved into a k...

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Autores principales: Yu, Xiaobo, Hartmann, Michael, Wang, Quan, Poetz, Oliver, Schneiderhan-Marra, Nicole, Stoll, Dieter, Kazmaier, Cornelia, Joos, Thomas O.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2948516/
https://www.ncbi.nlm.nih.gov/pubmed/20957050
http://dx.doi.org/10.1371/journal.pone.0013125
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author Yu, Xiaobo
Hartmann, Michael
Wang, Quan
Poetz, Oliver
Schneiderhan-Marra, Nicole
Stoll, Dieter
Kazmaier, Cornelia
Joos, Thomas O.
author_facet Yu, Xiaobo
Hartmann, Michael
Wang, Quan
Poetz, Oliver
Schneiderhan-Marra, Nicole
Stoll, Dieter
Kazmaier, Cornelia
Joos, Thomas O.
author_sort Yu, Xiaobo
collection PubMed
description BACKGROUND: Over the last ten years, miniaturized multiplexed immunoassays have become robust, reliable research tools that enable researchers to simultaneously determine a multitude of parameters. Among the numerous analytical protein arrays available, bead-based assay systems have evolved into a key technology that enables the quantitative protein profiling of biological samples whilst requiring only a minimal amount of sample material. METHODOLOGY/PRINCIPAL FINDINGS: A microfluidic bead-based immunoassay, µFBI, was developed to perform bead-based multiplexed sandwich immunoassays in a capillary. This setup allows the simultaneous detection of several parameters and only requires 200 ng of tissue lysate in a 1 µL assay volume. In addition, only 1 µL of detection antibodies and 1 µL of the reporter molecule Streptavidin-Phycoerythrin were required. The µFBI was used to compare the expression of seven receptor tyrosine kinases and their degree of tyrosine phosphorylation in breast cancer tissue and in normal tissue lysates. The total amount of HER-2, as well the degree of tyrosine phosphorylation was much higher in breast cancer tissue than in normal tissue. µFBI and a standard bead-based assay led to identical protein expression data. Moreover, it was possible to reduce the quantity of sample material required by a factor of 100 and the quantity of reagents by a factor of 30. CONCLUSIONS/SIGNIFICANCE: The µFBI, microfluidic bead-based immunoassay, allows the analysis of multiple parameters from a very small amount of sample material, such as tumor biopsies or tissue sections.
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spelling pubmed-29485162010-10-18 µFBI: A Microfluidic Bead-Based Immunoassay for Multiplexed Detection of Proteins from a µL Sample Volume Yu, Xiaobo Hartmann, Michael Wang, Quan Poetz, Oliver Schneiderhan-Marra, Nicole Stoll, Dieter Kazmaier, Cornelia Joos, Thomas O. PLoS One Research Article BACKGROUND: Over the last ten years, miniaturized multiplexed immunoassays have become robust, reliable research tools that enable researchers to simultaneously determine a multitude of parameters. Among the numerous analytical protein arrays available, bead-based assay systems have evolved into a key technology that enables the quantitative protein profiling of biological samples whilst requiring only a minimal amount of sample material. METHODOLOGY/PRINCIPAL FINDINGS: A microfluidic bead-based immunoassay, µFBI, was developed to perform bead-based multiplexed sandwich immunoassays in a capillary. This setup allows the simultaneous detection of several parameters and only requires 200 ng of tissue lysate in a 1 µL assay volume. In addition, only 1 µL of detection antibodies and 1 µL of the reporter molecule Streptavidin-Phycoerythrin were required. The µFBI was used to compare the expression of seven receptor tyrosine kinases and their degree of tyrosine phosphorylation in breast cancer tissue and in normal tissue lysates. The total amount of HER-2, as well the degree of tyrosine phosphorylation was much higher in breast cancer tissue than in normal tissue. µFBI and a standard bead-based assay led to identical protein expression data. Moreover, it was possible to reduce the quantity of sample material required by a factor of 100 and the quantity of reagents by a factor of 30. CONCLUSIONS/SIGNIFICANCE: The µFBI, microfluidic bead-based immunoassay, allows the analysis of multiple parameters from a very small amount of sample material, such as tumor biopsies or tissue sections. Public Library of Science 2010-10-01 /pmc/articles/PMC2948516/ /pubmed/20957050 http://dx.doi.org/10.1371/journal.pone.0013125 Text en Yu 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
Yu, Xiaobo
Hartmann, Michael
Wang, Quan
Poetz, Oliver
Schneiderhan-Marra, Nicole
Stoll, Dieter
Kazmaier, Cornelia
Joos, Thomas O.
µFBI: A Microfluidic Bead-Based Immunoassay for Multiplexed Detection of Proteins from a µL Sample Volume
title µFBI: A Microfluidic Bead-Based Immunoassay for Multiplexed Detection of Proteins from a µL Sample Volume
title_full µFBI: A Microfluidic Bead-Based Immunoassay for Multiplexed Detection of Proteins from a µL Sample Volume
title_fullStr µFBI: A Microfluidic Bead-Based Immunoassay for Multiplexed Detection of Proteins from a µL Sample Volume
title_full_unstemmed µFBI: A Microfluidic Bead-Based Immunoassay for Multiplexed Detection of Proteins from a µL Sample Volume
title_short µFBI: A Microfluidic Bead-Based Immunoassay for Multiplexed Detection of Proteins from a µL Sample Volume
title_sort µfbi: a microfluidic bead-based immunoassay for multiplexed detection of proteins from a µl sample volume
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2948516/
https://www.ncbi.nlm.nih.gov/pubmed/20957050
http://dx.doi.org/10.1371/journal.pone.0013125
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