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Profiling Inflammatory Responses with Microfluidic Immunoblotting

Rapid profiling of signaling pathways has been a long sought after goal in biological sciences and clinical medicine. To understand these signaling pathways, their protein components must be profiled. The protein components of signaling pathways are typically profiled with protein immunoblotting. Pr...

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Autores principales: Chang, Huai-Ning, Leroueil, Pascale R., Selwa, Katherine, Gasper, C. J., Tsuchida, Ryan E., Wang, Jason J., McHugh, Walker M., Cornell, Timothy T., Baker, James R., Goonewardena, Sascha N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842271/
https://www.ncbi.nlm.nih.gov/pubmed/24312374
http://dx.doi.org/10.1371/journal.pone.0081889
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author Chang, Huai-Ning
Leroueil, Pascale R.
Selwa, Katherine
Gasper, C. J.
Tsuchida, Ryan E.
Wang, Jason J.
McHugh, Walker M.
Cornell, Timothy T.
Baker, James R.
Goonewardena, Sascha N.
author_facet Chang, Huai-Ning
Leroueil, Pascale R.
Selwa, Katherine
Gasper, C. J.
Tsuchida, Ryan E.
Wang, Jason J.
McHugh, Walker M.
Cornell, Timothy T.
Baker, James R.
Goonewardena, Sascha N.
author_sort Chang, Huai-Ning
collection PubMed
description Rapid profiling of signaling pathways has been a long sought after goal in biological sciences and clinical medicine. To understand these signaling pathways, their protein components must be profiled. The protein components of signaling pathways are typically profiled with protein immunoblotting. Protein immunoblotting is a powerful technique but has several limitations including the large sample requirements, high amounts of antibody, and limitations in assay throughput. To overcome some of these limitations, we have designed a microfluidic protein immunoblotting device to profile multiple signaling pathways simultaneously. We show the utility of this approach by profiling inflammatory signaling pathways (NFκB, JAK-STAT, and MAPK) in cell models and human samples. The microfluidic immunoblotting device can profile proteins and protein modifications with 5380-fold less antibody compared to traditional protein immunoblotting. Additionally, this microfluidic device interfaces with commonly available immunoblotting equipment, has the ability to multiplex, and is compatible with several protein detection methodologies. We anticipate that this microfluidic device will complement existing techniques and is well suited for life science applications.
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spelling pubmed-38422712013-12-05 Profiling Inflammatory Responses with Microfluidic Immunoblotting Chang, Huai-Ning Leroueil, Pascale R. Selwa, Katherine Gasper, C. J. Tsuchida, Ryan E. Wang, Jason J. McHugh, Walker M. Cornell, Timothy T. Baker, James R. Goonewardena, Sascha N. PLoS One Research Article Rapid profiling of signaling pathways has been a long sought after goal in biological sciences and clinical medicine. To understand these signaling pathways, their protein components must be profiled. The protein components of signaling pathways are typically profiled with protein immunoblotting. Protein immunoblotting is a powerful technique but has several limitations including the large sample requirements, high amounts of antibody, and limitations in assay throughput. To overcome some of these limitations, we have designed a microfluidic protein immunoblotting device to profile multiple signaling pathways simultaneously. We show the utility of this approach by profiling inflammatory signaling pathways (NFκB, JAK-STAT, and MAPK) in cell models and human samples. The microfluidic immunoblotting device can profile proteins and protein modifications with 5380-fold less antibody compared to traditional protein immunoblotting. Additionally, this microfluidic device interfaces with commonly available immunoblotting equipment, has the ability to multiplex, and is compatible with several protein detection methodologies. We anticipate that this microfluidic device will complement existing techniques and is well suited for life science applications. Public Library of Science 2013-11-27 /pmc/articles/PMC3842271/ /pubmed/24312374 http://dx.doi.org/10.1371/journal.pone.0081889 Text en © 2013 Chang 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
Chang, Huai-Ning
Leroueil, Pascale R.
Selwa, Katherine
Gasper, C. J.
Tsuchida, Ryan E.
Wang, Jason J.
McHugh, Walker M.
Cornell, Timothy T.
Baker, James R.
Goonewardena, Sascha N.
Profiling Inflammatory Responses with Microfluidic Immunoblotting
title Profiling Inflammatory Responses with Microfluidic Immunoblotting
title_full Profiling Inflammatory Responses with Microfluidic Immunoblotting
title_fullStr Profiling Inflammatory Responses with Microfluidic Immunoblotting
title_full_unstemmed Profiling Inflammatory Responses with Microfluidic Immunoblotting
title_short Profiling Inflammatory Responses with Microfluidic Immunoblotting
title_sort profiling inflammatory responses with microfluidic immunoblotting
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842271/
https://www.ncbi.nlm.nih.gov/pubmed/24312374
http://dx.doi.org/10.1371/journal.pone.0081889
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