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Endogenous Carbamylation of Renal Medullary Proteins
Protein carbamylation is a post-translational modification that can occur in the presence of urea. In solution, urea is in equilibrium with ammonium cyanate, and carbamylation occurs when cyanate ions react with the amino groups of lysines, arginines, protein N-termini, as well as sulfhydryl groups...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873256/ https://www.ncbi.nlm.nih.gov/pubmed/24386107 http://dx.doi.org/10.1371/journal.pone.0082655 |
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author | Claxton, J'Neka S. Sandoval, Pablo C. Liu, Gary Chou, Chung-Lin Hoffert, Jason D. Knepper, Mark A. |
author_facet | Claxton, J'Neka S. Sandoval, Pablo C. Liu, Gary Chou, Chung-Lin Hoffert, Jason D. Knepper, Mark A. |
author_sort | Claxton, J'Neka S. |
collection | PubMed |
description | Protein carbamylation is a post-translational modification that can occur in the presence of urea. In solution, urea is in equilibrium with ammonium cyanate, and carbamylation occurs when cyanate ions react with the amino groups of lysines, arginines, protein N-termini, as well as sulfhydryl groups of cysteines. The concentration of urea is elevated in the renal inner medulla compared with other tissues. Due to the high urea concentration, we hypothesized that carbamylation can occur endogenously within the rat inner medulla. Using immunoblotting of rat kidney cortical and medullary homogenates with a carbamyl-lysine specific antibody, we showed that carbamylation is present in a large number of inner medullary proteins. Using protein mass spectrometry (LC-MS/MS) of rat renal inner medulla, we identified 456 unique carbamylated sites in 403 proteins, including many that play important physiological roles in the renal medulla [Data can be accessed at https://helixweb.nih.gov/ESBL/Database/Carbamylation/Carbamylation_peptide_sorted.html]. We conclude that protein carbamylation occurs endogenously in the kidney, modifying many physiologically important proteins. |
format | Online Article Text |
id | pubmed-3873256 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38732562014-01-02 Endogenous Carbamylation of Renal Medullary Proteins Claxton, J'Neka S. Sandoval, Pablo C. Liu, Gary Chou, Chung-Lin Hoffert, Jason D. Knepper, Mark A. PLoS One Research Article Protein carbamylation is a post-translational modification that can occur in the presence of urea. In solution, urea is in equilibrium with ammonium cyanate, and carbamylation occurs when cyanate ions react with the amino groups of lysines, arginines, protein N-termini, as well as sulfhydryl groups of cysteines. The concentration of urea is elevated in the renal inner medulla compared with other tissues. Due to the high urea concentration, we hypothesized that carbamylation can occur endogenously within the rat inner medulla. Using immunoblotting of rat kidney cortical and medullary homogenates with a carbamyl-lysine specific antibody, we showed that carbamylation is present in a large number of inner medullary proteins. Using protein mass spectrometry (LC-MS/MS) of rat renal inner medulla, we identified 456 unique carbamylated sites in 403 proteins, including many that play important physiological roles in the renal medulla [Data can be accessed at https://helixweb.nih.gov/ESBL/Database/Carbamylation/Carbamylation_peptide_sorted.html]. We conclude that protein carbamylation occurs endogenously in the kidney, modifying many physiologically important proteins. Public Library of Science 2013-12-26 /pmc/articles/PMC3873256/ /pubmed/24386107 http://dx.doi.org/10.1371/journal.pone.0082655 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Claxton, J'Neka S. Sandoval, Pablo C. Liu, Gary Chou, Chung-Lin Hoffert, Jason D. Knepper, Mark A. Endogenous Carbamylation of Renal Medullary Proteins |
title | Endogenous Carbamylation of Renal Medullary Proteins |
title_full | Endogenous Carbamylation of Renal Medullary Proteins |
title_fullStr | Endogenous Carbamylation of Renal Medullary Proteins |
title_full_unstemmed | Endogenous Carbamylation of Renal Medullary Proteins |
title_short | Endogenous Carbamylation of Renal Medullary Proteins |
title_sort | endogenous carbamylation of renal medullary proteins |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873256/ https://www.ncbi.nlm.nih.gov/pubmed/24386107 http://dx.doi.org/10.1371/journal.pone.0082655 |
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