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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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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. |
format | Online Article Text |
id | pubmed-4319709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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