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Global profiling of protein lipidation using chemical proteomic technologies

Protein lipidation is unique amongst post-translational modifications (PTMs) in enabling direct interaction with cell membranes, and is found in every form of life. Lipidation is important in normal function and in disease, but its intricate interplay with disease context presents a challenging for...

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Detalles Bibliográficos
Autores principales: Tate, Edward W, Kalesh, Karunakaran A, Lanyon-Hogg, Thomas, Storck, Elisabeth M, Thinon, Emmanuelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4319709/
https://www.ncbi.nlm.nih.gov/pubmed/25461723
http://dx.doi.org/10.1016/j.cbpa.2014.10.016
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author Tate, Edward W
Kalesh, Karunakaran A
Lanyon-Hogg, Thomas
Storck, Elisabeth M
Thinon, Emmanuelle
author_facet Tate, Edward W
Kalesh, Karunakaran A
Lanyon-Hogg, Thomas
Storck, Elisabeth M
Thinon, Emmanuelle
author_sort Tate, Edward W
collection PubMed
description Protein lipidation is unique amongst post-translational modifications (PTMs) in enabling direct interaction with cell membranes, and is found in every form of life. Lipidation is important in normal function and in disease, but its intricate interplay with disease context presents a challenging for drug development. Global whole-proteome profiling of protein lipidation lies beyond the range of standard methods, but is well-suited to metabolic tagging with small ‘clickable’ chemical reporters that do not disrupt metabolism and function; chemoselective reactions are then used to add multifunctional labels exclusively to tagged-lipidated proteins. This chemical proteomic technology has opened up the first quantitative whole-proteome studies of the known major classes of protein lipidation, and the first insights into their full scope in vivo.
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spelling pubmed-43197092015-02-09 Global profiling of protein lipidation using chemical proteomic technologies Tate, Edward W Kalesh, Karunakaran A Lanyon-Hogg, Thomas Storck, Elisabeth M Thinon, Emmanuelle Curr Opin Chem Biol Article Protein lipidation is unique amongst post-translational modifications (PTMs) in enabling direct interaction with cell membranes, and is found in every form of life. Lipidation is important in normal function and in disease, but its intricate interplay with disease context presents a challenging for drug development. Global whole-proteome profiling of protein lipidation lies beyond the range of standard methods, but is well-suited to metabolic tagging with small ‘clickable’ chemical reporters that do not disrupt metabolism and function; chemoselective reactions are then used to add multifunctional labels exclusively to tagged-lipidated proteins. This chemical proteomic technology has opened up the first quantitative whole-proteome studies of the known major classes of protein lipidation, and the first insights into their full scope in vivo. Elsevier 2015-02 /pmc/articles/PMC4319709/ /pubmed/25461723 http://dx.doi.org/10.1016/j.cbpa.2014.10.016 Text en © 2014 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Tate, Edward W
Kalesh, Karunakaran A
Lanyon-Hogg, Thomas
Storck, Elisabeth M
Thinon, Emmanuelle
Global profiling of protein lipidation using chemical proteomic technologies
title Global profiling of protein lipidation using chemical proteomic technologies
title_full Global profiling of protein lipidation using chemical proteomic technologies
title_fullStr Global profiling of protein lipidation using chemical proteomic technologies
title_full_unstemmed Global profiling of protein lipidation using chemical proteomic technologies
title_short Global profiling of protein lipidation using chemical proteomic technologies
title_sort global profiling of protein lipidation using chemical proteomic technologies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4319709/
https://www.ncbi.nlm.nih.gov/pubmed/25461723
http://dx.doi.org/10.1016/j.cbpa.2014.10.016
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