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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...

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Detalles Bibliográficos
Autores principales: Firulli, Beth A., Virshup, David M., Firulli, Anthony B.
Formato: Texto
Lenguaje:English
Publicado: Biological Procedures Online 2004
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.
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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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