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Quantitative Dynamics of Phosphoproteome: The Devil Is in the Details
[Image: see text] Recent advances in peptide-based (bottom-up) quantitative proteomics and bioinformatics have opened unprecedented opportunities for extensive investigation of cellular proteomes and their dynamics. Here we discuss two approaches currently used to investigate the global dynamics of...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3477822/ https://www.ncbi.nlm.nih.gov/pubmed/23020125 http://dx.doi.org/10.1021/ac301833k |
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author | Salek, Mogjiborahman Acuto, Oreste |
author_facet | Salek, Mogjiborahman Acuto, Oreste |
author_sort | Salek, Mogjiborahman |
collection | PubMed |
description | [Image: see text] Recent advances in peptide-based (bottom-up) quantitative proteomics and bioinformatics have opened unprecedented opportunities for extensive investigation of cellular proteomes and their dynamics. Here we discuss two approaches currently used to investigate the global dynamics of phosphorylation based on the isolation of phosphorylated proteins or peptides. We evaluate the accuracy of these methodologies to grasp the global dynamics of phosphorylation, and we raise awareness on ambiguities inherent to these analyses. We conclude that further development of targeted approaches should prevent inaccurate conclusions about the nature of biological regulations and in particular kinase-substrate networks. |
format | Online Article Text |
id | pubmed-3477822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-34778222012-10-22 Quantitative Dynamics of Phosphoproteome: The Devil Is in the Details Salek, Mogjiborahman Acuto, Oreste Anal Chem [Image: see text] Recent advances in peptide-based (bottom-up) quantitative proteomics and bioinformatics have opened unprecedented opportunities for extensive investigation of cellular proteomes and their dynamics. Here we discuss two approaches currently used to investigate the global dynamics of phosphorylation based on the isolation of phosphorylated proteins or peptides. We evaluate the accuracy of these methodologies to grasp the global dynamics of phosphorylation, and we raise awareness on ambiguities inherent to these analyses. We conclude that further development of targeted approaches should prevent inaccurate conclusions about the nature of biological regulations and in particular kinase-substrate networks. American Chemical Society 2012-09-28 2012-10-16 /pmc/articles/PMC3477822/ /pubmed/23020125 http://dx.doi.org/10.1021/ac301833k Text en Copyright © 2012 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org. |
spellingShingle | Salek, Mogjiborahman Acuto, Oreste Quantitative Dynamics of Phosphoproteome: The Devil Is in the Details |
title | Quantitative Dynamics
of Phosphoproteome: The Devil
Is in the Details |
title_full | Quantitative Dynamics
of Phosphoproteome: The Devil
Is in the Details |
title_fullStr | Quantitative Dynamics
of Phosphoproteome: The Devil
Is in the Details |
title_full_unstemmed | Quantitative Dynamics
of Phosphoproteome: The Devil
Is in the Details |
title_short | Quantitative Dynamics
of Phosphoproteome: The Devil
Is in the Details |
title_sort | quantitative dynamics
of phosphoproteome: the devil
is in the details |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3477822/ https://www.ncbi.nlm.nih.gov/pubmed/23020125 http://dx.doi.org/10.1021/ac301833k |
work_keys_str_mv | AT salekmogjiborahman quantitativedynamicsofphosphoproteomethedevilisinthedetails AT acutooreste quantitativedynamicsofphosphoproteomethedevilisinthedetails |