Cargando…
Optimized sample preparation for two-dimensional gel electrophoresis of soluble proteins from chicken bursa of Fabricius
BACKGROUND: Two-dimensional gel electrophoresis (2-DE) is a powerful method to study protein expression and function in living organisms and diseases. This technique, however, has not been applied to avian bursa of Fabricius (BF), a central immune organ. Here, optimized 2-DE sample preparation metho...
Autores principales: | , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2770044/ https://www.ncbi.nlm.nih.gov/pubmed/19814785 http://dx.doi.org/10.1186/1477-5956-7-38 |
_version_ | 1782173618825854976 |
---|---|
author | Wu, Yongping Zhou, Jiyong Zhang, Xin Zheng, Xiaojuan Jiang, Xuetao Shi, Lixue Yin, Wei Wang, Junhua |
author_facet | Wu, Yongping Zhou, Jiyong Zhang, Xin Zheng, Xiaojuan Jiang, Xuetao Shi, Lixue Yin, Wei Wang, Junhua |
author_sort | Wu, Yongping |
collection | PubMed |
description | BACKGROUND: Two-dimensional gel electrophoresis (2-DE) is a powerful method to study protein expression and function in living organisms and diseases. This technique, however, has not been applied to avian bursa of Fabricius (BF), a central immune organ. Here, optimized 2-DE sample preparation methodologies were constructed for the chicken BF tissue. Using the optimized protocol, we performed further 2-DE analysis on a soluble protein extract from the BF of chickens infected with virulent avibirnavirus. To demonstrate the quality of the extracted proteins, several differentially expressed protein spots selected were cut from 2-DE gels and identified by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS). RESULTS: An extraction buffer containing 7 M urea, 2 M thiourea, 2% (w/v) 3-[(3-cholamidopropyl)-dimethylammonio]-1-propanesulfonate (CHAPS), 50 mM dithiothreitol (DTT), 0.2% Bio-Lyte 3/10, 1 mM phenylmethylsulfonyl fluoride (PMSF), 20 U/ml Deoxyribonuclease I (DNase I), and 0.25 mg/ml Ribonuclease A (RNase A), combined with sonication and vortex, yielded the best 2-DE data. Relative to non-frozen immobilized pH gradient (IPG) strips, frozen IPG strips did not result in significant changes in the 2-DE patterns after isoelectric focusing (IEF). When the optimized protocol was used to analyze the spleen and thymus, as well as avibirnavirus-infected bursa, high quality 2-DE protein expression profiles were obtained. 2-DE maps of BF of chickens infected with virulent avibirnavirus were visibly different and many differentially expressed proteins were found. CONCLUSION: These results showed that method C, in concert extraction buffer IV, was the most favorable for preparing samples for IEF and subsequent protein separation and yielded the best quality 2-DE patterns. The optimized protocol is a useful sample preparation method for comparative proteomics analysis of chicken BF tissues. |
format | Text |
id | pubmed-2770044 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27700442009-10-29 Optimized sample preparation for two-dimensional gel electrophoresis of soluble proteins from chicken bursa of Fabricius Wu, Yongping Zhou, Jiyong Zhang, Xin Zheng, Xiaojuan Jiang, Xuetao Shi, Lixue Yin, Wei Wang, Junhua Proteome Sci Methodology BACKGROUND: Two-dimensional gel electrophoresis (2-DE) is a powerful method to study protein expression and function in living organisms and diseases. This technique, however, has not been applied to avian bursa of Fabricius (BF), a central immune organ. Here, optimized 2-DE sample preparation methodologies were constructed for the chicken BF tissue. Using the optimized protocol, we performed further 2-DE analysis on a soluble protein extract from the BF of chickens infected with virulent avibirnavirus. To demonstrate the quality of the extracted proteins, several differentially expressed protein spots selected were cut from 2-DE gels and identified by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS). RESULTS: An extraction buffer containing 7 M urea, 2 M thiourea, 2% (w/v) 3-[(3-cholamidopropyl)-dimethylammonio]-1-propanesulfonate (CHAPS), 50 mM dithiothreitol (DTT), 0.2% Bio-Lyte 3/10, 1 mM phenylmethylsulfonyl fluoride (PMSF), 20 U/ml Deoxyribonuclease I (DNase I), and 0.25 mg/ml Ribonuclease A (RNase A), combined with sonication and vortex, yielded the best 2-DE data. Relative to non-frozen immobilized pH gradient (IPG) strips, frozen IPG strips did not result in significant changes in the 2-DE patterns after isoelectric focusing (IEF). When the optimized protocol was used to analyze the spleen and thymus, as well as avibirnavirus-infected bursa, high quality 2-DE protein expression profiles were obtained. 2-DE maps of BF of chickens infected with virulent avibirnavirus were visibly different and many differentially expressed proteins were found. CONCLUSION: These results showed that method C, in concert extraction buffer IV, was the most favorable for preparing samples for IEF and subsequent protein separation and yielded the best quality 2-DE patterns. The optimized protocol is a useful sample preparation method for comparative proteomics analysis of chicken BF tissues. BioMed Central 2009-10-08 /pmc/articles/PMC2770044/ /pubmed/19814785 http://dx.doi.org/10.1186/1477-5956-7-38 Text en Copyright © 2009 Wu et al; licensee BioMed Central Ltd. 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 Wu, Yongping Zhou, Jiyong Zhang, Xin Zheng, Xiaojuan Jiang, Xuetao Shi, Lixue Yin, Wei Wang, Junhua Optimized sample preparation for two-dimensional gel electrophoresis of soluble proteins from chicken bursa of Fabricius |
title | Optimized sample preparation for two-dimensional gel electrophoresis of soluble proteins from chicken bursa of Fabricius |
title_full | Optimized sample preparation for two-dimensional gel electrophoresis of soluble proteins from chicken bursa of Fabricius |
title_fullStr | Optimized sample preparation for two-dimensional gel electrophoresis of soluble proteins from chicken bursa of Fabricius |
title_full_unstemmed | Optimized sample preparation for two-dimensional gel electrophoresis of soluble proteins from chicken bursa of Fabricius |
title_short | Optimized sample preparation for two-dimensional gel electrophoresis of soluble proteins from chicken bursa of Fabricius |
title_sort | optimized sample preparation for two-dimensional gel electrophoresis of soluble proteins from chicken bursa of fabricius |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2770044/ https://www.ncbi.nlm.nih.gov/pubmed/19814785 http://dx.doi.org/10.1186/1477-5956-7-38 |
work_keys_str_mv | AT wuyongping optimizedsamplepreparationfortwodimensionalgelelectrophoresisofsolubleproteinsfromchickenbursaoffabricius AT zhoujiyong optimizedsamplepreparationfortwodimensionalgelelectrophoresisofsolubleproteinsfromchickenbursaoffabricius AT zhangxin optimizedsamplepreparationfortwodimensionalgelelectrophoresisofsolubleproteinsfromchickenbursaoffabricius AT zhengxiaojuan optimizedsamplepreparationfortwodimensionalgelelectrophoresisofsolubleproteinsfromchickenbursaoffabricius AT jiangxuetao optimizedsamplepreparationfortwodimensionalgelelectrophoresisofsolubleproteinsfromchickenbursaoffabricius AT shilixue optimizedsamplepreparationfortwodimensionalgelelectrophoresisofsolubleproteinsfromchickenbursaoffabricius AT yinwei optimizedsamplepreparationfortwodimensionalgelelectrophoresisofsolubleproteinsfromchickenbursaoffabricius AT wangjunhua optimizedsamplepreparationfortwodimensionalgelelectrophoresisofsolubleproteinsfromchickenbursaoffabricius |