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Phosphopeptide mapping of proteins ectopically expressed in tissue culture cell lines
Post-translational modifications such as phosphorylation play a vital role in the regulation of protein function. In our study of the basic Helix-loop-Helix (bHLH) transcription factor HAND1, it was suspected that HAND1 was being phosphorylated during trophoblast giant cell differentiation and that...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Biological Procedures Online
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC389901/ https://www.ncbi.nlm.nih.gov/pubmed/15103396 http://dx.doi.org/10.1251/bpo69 |
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author | Firulli, Beth A. Virshup, David M. Firulli, Anthony B. |
author_facet | Firulli, Beth A. Virshup, David M. Firulli, Anthony B. |
author_sort | Firulli, Beth A. |
collection | PubMed |
description | Post-translational modifications such as phosphorylation play a vital role in the regulation of protein function. In our study of the basic Helix-loop-Helix (bHLH) transcription factor HAND1, it was suspected that HAND1 was being phosphorylated during trophoblast giant cell differentiation and that coexpression of a constitutively active kinase with HAND1 resulted in changes in the proteins dimerization profile. In order to accurately document HAND1 phosphorylation and identify the resides being modified, we employed metabolic cell labeling with (32)P of tissue culture cells coexpressing a Flag-epitope tagged HAND1 along with a number of active kinases and phosphatase subunits. We generated phosphopeptide maps of the phosphorylated HAND1 using the methods described below and linked these modifications to changes in HAND1 biological function. |
format | Text |
id | pubmed-389901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | Biological Procedures Online |
record_format | MEDLINE/PubMed |
spelling | pubmed-3899012004-04-20 Phosphopeptide mapping of proteins ectopically expressed in tissue culture cell lines Firulli, Beth A. Virshup, David M. Firulli, Anthony B. Biol Proced Online Research Article Post-translational modifications such as phosphorylation play a vital role in the regulation of protein function. In our study of the basic Helix-loop-Helix (bHLH) transcription factor HAND1, it was suspected that HAND1 was being phosphorylated during trophoblast giant cell differentiation and that coexpression of a constitutively active kinase with HAND1 resulted in changes in the proteins dimerization profile. In order to accurately document HAND1 phosphorylation and identify the resides being modified, we employed metabolic cell labeling with (32)P of tissue culture cells coexpressing a Flag-epitope tagged HAND1 along with a number of active kinases and phosphatase subunits. We generated phosphopeptide maps of the phosphorylated HAND1 using the methods described below and linked these modifications to changes in HAND1 biological function. Biological Procedures Online 2004-03-19 /pmc/articles/PMC389901/ /pubmed/15103396 http://dx.doi.org/10.1251/bpo69 Text en Copyright © March 03, 2004, BA Firulli et al. Published in Biological Procedures Online under license from the authors. Copying, printing, redistribution and storage permitted. |
spellingShingle | Research Article Firulli, Beth A. Virshup, David M. Firulli, Anthony B. Phosphopeptide mapping of proteins ectopically expressed in tissue culture cell lines |
title | Phosphopeptide mapping of proteins ectopically expressed in tissue culture cell lines |
title_full | Phosphopeptide mapping of proteins ectopically expressed in tissue culture cell lines |
title_fullStr | Phosphopeptide mapping of proteins ectopically expressed in tissue culture cell lines |
title_full_unstemmed | Phosphopeptide mapping of proteins ectopically expressed in tissue culture cell lines |
title_short | Phosphopeptide mapping of proteins ectopically expressed in tissue culture cell lines |
title_sort | phosphopeptide mapping of proteins ectopically expressed in tissue culture cell lines |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC389901/ https://www.ncbi.nlm.nih.gov/pubmed/15103396 http://dx.doi.org/10.1251/bpo69 |
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