Cargando…

Chemical Proteomic Platform To Identify Citrullinated Proteins

[Image: see text] Anti-citrullinated protein antibodies (ACPAs) are a hallmark of rheumatoid arthritis (RA) and are routinely used for disease diagnosis. Protein citrullination is also increased in cancer and other autoimmune disorders, suggesting that citrullinated proteins may serve as biomarkers...

Descripción completa

Detalles Bibliográficos
Autores principales: Lewallen, Daniel M., Bicker, Kevin L., Subramanian, Venkataraman, Clancy, Kathleen W., Slade, Daniel J., Martell, Julianne, Dreyton, Christina J., Sokolove, Jeremy, Weerapana, Eranthie, Thompson, Paul R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2015
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4729336/
https://www.ncbi.nlm.nih.gov/pubmed/26360112
http://dx.doi.org/10.1021/acschembio.5b00438
_version_ 1782412246300753920
author Lewallen, Daniel M.
Bicker, Kevin L.
Subramanian, Venkataraman
Clancy, Kathleen W.
Slade, Daniel J.
Martell, Julianne
Dreyton, Christina J.
Sokolove, Jeremy
Weerapana, Eranthie
Thompson, Paul R.
author_facet Lewallen, Daniel M.
Bicker, Kevin L.
Subramanian, Venkataraman
Clancy, Kathleen W.
Slade, Daniel J.
Martell, Julianne
Dreyton, Christina J.
Sokolove, Jeremy
Weerapana, Eranthie
Thompson, Paul R.
author_sort Lewallen, Daniel M.
collection PubMed
description [Image: see text] Anti-citrullinated protein antibodies (ACPAs) are a hallmark of rheumatoid arthritis (RA) and are routinely used for disease diagnosis. Protein citrullination is also increased in cancer and other autoimmune disorders, suggesting that citrullinated proteins may serve as biomarkers for diseases beyond RA. To identify these citrullinated proteins, we developed biotin-conjugated phenylglyoxal (biotin-PG). Using this probe and our platform technology, we identified >50 intracellular citrullinated proteins. More than 20 of these are involved in RNA splicing, suggesting, for the first time, that citrullination modulates RNA biology. Overall, this chemical proteomic platform will play a key role in furthering our understanding of protein citrullination in rheumatoid arthritis and potentially a wider spectrum of inflammatory diseases.
format Online
Article
Text
id pubmed-4729336
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-47293362016-02-10 Chemical Proteomic Platform To Identify Citrullinated Proteins Lewallen, Daniel M. Bicker, Kevin L. Subramanian, Venkataraman Clancy, Kathleen W. Slade, Daniel J. Martell, Julianne Dreyton, Christina J. Sokolove, Jeremy Weerapana, Eranthie Thompson, Paul R. ACS Chem Biol [Image: see text] Anti-citrullinated protein antibodies (ACPAs) are a hallmark of rheumatoid arthritis (RA) and are routinely used for disease diagnosis. Protein citrullination is also increased in cancer and other autoimmune disorders, suggesting that citrullinated proteins may serve as biomarkers for diseases beyond RA. To identify these citrullinated proteins, we developed biotin-conjugated phenylglyoxal (biotin-PG). Using this probe and our platform technology, we identified >50 intracellular citrullinated proteins. More than 20 of these are involved in RNA splicing, suggesting, for the first time, that citrullination modulates RNA biology. Overall, this chemical proteomic platform will play a key role in furthering our understanding of protein citrullination in rheumatoid arthritis and potentially a wider spectrum of inflammatory diseases. American Chemical Society 2015-09-11 2015-11-20 /pmc/articles/PMC4729336/ /pubmed/26360112 http://dx.doi.org/10.1021/acschembio.5b00438 Text en Copyright © 2015 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Lewallen, Daniel M.
Bicker, Kevin L.
Subramanian, Venkataraman
Clancy, Kathleen W.
Slade, Daniel J.
Martell, Julianne
Dreyton, Christina J.
Sokolove, Jeremy
Weerapana, Eranthie
Thompson, Paul R.
Chemical Proteomic Platform To Identify Citrullinated Proteins
title Chemical Proteomic Platform To Identify Citrullinated Proteins
title_full Chemical Proteomic Platform To Identify Citrullinated Proteins
title_fullStr Chemical Proteomic Platform To Identify Citrullinated Proteins
title_full_unstemmed Chemical Proteomic Platform To Identify Citrullinated Proteins
title_short Chemical Proteomic Platform To Identify Citrullinated Proteins
title_sort chemical proteomic platform to identify citrullinated proteins
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4729336/
https://www.ncbi.nlm.nih.gov/pubmed/26360112
http://dx.doi.org/10.1021/acschembio.5b00438
work_keys_str_mv AT lewallendanielm chemicalproteomicplatformtoidentifycitrullinatedproteins
AT bickerkevinl chemicalproteomicplatformtoidentifycitrullinatedproteins
AT subramanianvenkataraman chemicalproteomicplatformtoidentifycitrullinatedproteins
AT clancykathleenw chemicalproteomicplatformtoidentifycitrullinatedproteins
AT sladedanielj chemicalproteomicplatformtoidentifycitrullinatedproteins
AT martelljulianne chemicalproteomicplatformtoidentifycitrullinatedproteins
AT dreytonchristinaj chemicalproteomicplatformtoidentifycitrullinatedproteins
AT sokolovejeremy chemicalproteomicplatformtoidentifycitrullinatedproteins
AT weerapanaeranthie chemicalproteomicplatformtoidentifycitrullinatedproteins
AT thompsonpaulr chemicalproteomicplatformtoidentifycitrullinatedproteins