Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Salek, Mogjiborahman, Acuto, Oreste
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2012
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
_version_ 1782247260380200960
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