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A New Microsphere-Based Immunoassay for Measuring the Activity of Transcription Factors
There are several traditional and well-developed methods for analyzing the activity of transcription factors, such as EMSA, enzyme-linked immunosorbent assay, and reporter gene activity assays. All of these methods have their own distinct disadvantages, but none can analyze the changes in transcript...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3055901/ https://www.ncbi.nlm.nih.gov/pubmed/21406071 http://dx.doi.org/10.1007/s12575-010-9030-z |
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author | Lin, Yu-Ling Lai, Yun-Ju Tsai, Nu-Man Peng, Tai-Chu Liu, Yen-Ku Lee, Ru-Ping Tsai, Chueh-Jen Liao, Kuang-Wen |
author_facet | Lin, Yu-Ling Lai, Yun-Ju Tsai, Nu-Man Peng, Tai-Chu Liu, Yen-Ku Lee, Ru-Ping Tsai, Chueh-Jen Liao, Kuang-Wen |
author_sort | Lin, Yu-Ling |
collection | PubMed |
description | There are several traditional and well-developed methods for analyzing the activity of transcription factors, such as EMSA, enzyme-linked immunosorbent assay, and reporter gene activity assays. All of these methods have their own distinct disadvantages, but none can analyze the changes in transcription factors in the few cells that are cultured in the wells of 96-well titer plates. Thus, a new microsphere-based immunoassay to measure the activity of transcription factors (MIA-TF) was developed. In MIA-TF, NeutrAvidin-labeled microspheres were used as the solid phase to capture biotin-labeled double-strand DNA fragments which contain certain transcription factor binding elements. The activity of transcription factors was detected by immunoassay using a transcription factor-specific antibody to monitor the binding with the DNA probe. Next, analysis was performed by flow cytometry. The targets hypoxia-inducible factor-1α (HIF-1α) and nuclear factor-kappa B (NF-κB) were applied and detected in this MIA-TF method; the results that we obtained demonstrated that this method could be used to monitor the changes of NF-κB or HIF within 50 or 100 ng of nuclear extract. Furthermore, MIA-TF could detect the changes in NF-κB or HIF in cells that were cultured in wells of a 96-well plate without purification of the nuclear protein, an important consideration for applying this method to high-throughput assays in the future. The development of MIA-TF would support further progress in clinical analysis and drug screening systems. Overall, MIA-TF is a method with high potential to detect the activity of transcription factors. |
format | Text |
id | pubmed-3055901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30559012011-03-12 A New Microsphere-Based Immunoassay for Measuring the Activity of Transcription Factors Lin, Yu-Ling Lai, Yun-Ju Tsai, Nu-Man Peng, Tai-Chu Liu, Yen-Ku Lee, Ru-Ping Tsai, Chueh-Jen Liao, Kuang-Wen Biol Proced Online Methodology There are several traditional and well-developed methods for analyzing the activity of transcription factors, such as EMSA, enzyme-linked immunosorbent assay, and reporter gene activity assays. All of these methods have their own distinct disadvantages, but none can analyze the changes in transcription factors in the few cells that are cultured in the wells of 96-well titer plates. Thus, a new microsphere-based immunoassay to measure the activity of transcription factors (MIA-TF) was developed. In MIA-TF, NeutrAvidin-labeled microspheres were used as the solid phase to capture biotin-labeled double-strand DNA fragments which contain certain transcription factor binding elements. The activity of transcription factors was detected by immunoassay using a transcription factor-specific antibody to monitor the binding with the DNA probe. Next, analysis was performed by flow cytometry. The targets hypoxia-inducible factor-1α (HIF-1α) and nuclear factor-kappa B (NF-κB) were applied and detected in this MIA-TF method; the results that we obtained demonstrated that this method could be used to monitor the changes of NF-κB or HIF within 50 or 100 ng of nuclear extract. Furthermore, MIA-TF could detect the changes in NF-κB or HIF in cells that were cultured in wells of a 96-well plate without purification of the nuclear protein, an important consideration for applying this method to high-throughput assays in the future. The development of MIA-TF would support further progress in clinical analysis and drug screening systems. Overall, MIA-TF is a method with high potential to detect the activity of transcription factors. BioMed Central 2010-04-14 /pmc/articles/PMC3055901/ /pubmed/21406071 http://dx.doi.org/10.1007/s12575-010-9030-z Text en Copyright ©2010 Lin et al; licensee Springer http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Lin, Yu-Ling Lai, Yun-Ju Tsai, Nu-Man Peng, Tai-Chu Liu, Yen-Ku Lee, Ru-Ping Tsai, Chueh-Jen Liao, Kuang-Wen A New Microsphere-Based Immunoassay for Measuring the Activity of Transcription Factors |
title | A New Microsphere-Based Immunoassay for Measuring the Activity of Transcription Factors |
title_full | A New Microsphere-Based Immunoassay for Measuring the Activity of Transcription Factors |
title_fullStr | A New Microsphere-Based Immunoassay for Measuring the Activity of Transcription Factors |
title_full_unstemmed | A New Microsphere-Based Immunoassay for Measuring the Activity of Transcription Factors |
title_short | A New Microsphere-Based Immunoassay for Measuring the Activity of Transcription Factors |
title_sort | new microsphere-based immunoassay for measuring the activity of transcription factors |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3055901/ https://www.ncbi.nlm.nih.gov/pubmed/21406071 http://dx.doi.org/10.1007/s12575-010-9030-z |
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