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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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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. |
format | Online Article Text |
id | pubmed-3842271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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