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Comparison of Protein N-Homocysteinylation in Rat Plasma under Elevated Homocysteine Using a Specific Chemical Labeling Method

Elevated blood concentrations of homocysteine have been well established as a risk factor for cardiovascular diseases and neuropsychiatric diseases, yet the etiologic relationship of homocysteine to these disorders remains poorly understood. Protein N-homocysteinylation has been hypothesized as a co...

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Autores principales: Zang, Tianzhu, Pottenplackel, Ligi Paul, Handy, Diane E., Loscalzo, Joseph, Dai, Shujia, Deth, Richard C., Zhou, Zhaohui Sunny, Ma, Jisheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292613/
https://www.ncbi.nlm.nih.gov/pubmed/27617989
http://dx.doi.org/10.3390/molecules21091195
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author Zang, Tianzhu
Pottenplackel, Ligi Paul
Handy, Diane E.
Loscalzo, Joseph
Dai, Shujia
Deth, Richard C.
Zhou, Zhaohui Sunny
Ma, Jisheng
author_facet Zang, Tianzhu
Pottenplackel, Ligi Paul
Handy, Diane E.
Loscalzo, Joseph
Dai, Shujia
Deth, Richard C.
Zhou, Zhaohui Sunny
Ma, Jisheng
author_sort Zang, Tianzhu
collection PubMed
description Elevated blood concentrations of homocysteine have been well established as a risk factor for cardiovascular diseases and neuropsychiatric diseases, yet the etiologic relationship of homocysteine to these disorders remains poorly understood. Protein N-homocysteinylation has been hypothesized as a contributing factor; however, it has not been examined globally owing to the lack of suitable detection methods. We recently developed a selective chemical method to label N-homocysteinylated proteins with a biotin-aldehyde tag followed by Western blotting analysis, which was further optimized in this study. We then investigated the variation of protein N-homocysteinylation in plasma from rats on a vitamin B(12) deficient diet. Elevated “total homocysteine” concentrations were determined in rats with a vitamin B(12) deficient diet. Correspondingly, overall levels of plasma protein N-homocysteinylation displayed an increased trend, and furthermore, more pronounced and statistically significant changes (e.g., 1.8-fold, p-value: 0.03) were observed for some individual protein bands. Our results suggest that, as expected, a general metabolic correlation exists between “total homocysteine” and N-homocysteinylation, although other factors are involved in homocysteine/homocysteine thiolactone metabolism, such as the transsulfuration of homocysteine by cystathionine β-synthase or the hydrolysis of homocysteine thiolactone by paraoxonase 1 (PON1), may play more significant or direct roles in determining the level of N-homocysteinylation.
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spelling pubmed-52926132017-03-08 Comparison of Protein N-Homocysteinylation in Rat Plasma under Elevated Homocysteine Using a Specific Chemical Labeling Method Zang, Tianzhu Pottenplackel, Ligi Paul Handy, Diane E. Loscalzo, Joseph Dai, Shujia Deth, Richard C. Zhou, Zhaohui Sunny Ma, Jisheng Molecules Article Elevated blood concentrations of homocysteine have been well established as a risk factor for cardiovascular diseases and neuropsychiatric diseases, yet the etiologic relationship of homocysteine to these disorders remains poorly understood. Protein N-homocysteinylation has been hypothesized as a contributing factor; however, it has not been examined globally owing to the lack of suitable detection methods. We recently developed a selective chemical method to label N-homocysteinylated proteins with a biotin-aldehyde tag followed by Western blotting analysis, which was further optimized in this study. We then investigated the variation of protein N-homocysteinylation in plasma from rats on a vitamin B(12) deficient diet. Elevated “total homocysteine” concentrations were determined in rats with a vitamin B(12) deficient diet. Correspondingly, overall levels of plasma protein N-homocysteinylation displayed an increased trend, and furthermore, more pronounced and statistically significant changes (e.g., 1.8-fold, p-value: 0.03) were observed for some individual protein bands. Our results suggest that, as expected, a general metabolic correlation exists between “total homocysteine” and N-homocysteinylation, although other factors are involved in homocysteine/homocysteine thiolactone metabolism, such as the transsulfuration of homocysteine by cystathionine β-synthase or the hydrolysis of homocysteine thiolactone by paraoxonase 1 (PON1), may play more significant or direct roles in determining the level of N-homocysteinylation. MDPI 2016-09-08 /pmc/articles/PMC5292613/ /pubmed/27617989 http://dx.doi.org/10.3390/molecules21091195 Text en © 2016 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zang, Tianzhu
Pottenplackel, Ligi Paul
Handy, Diane E.
Loscalzo, Joseph
Dai, Shujia
Deth, Richard C.
Zhou, Zhaohui Sunny
Ma, Jisheng
Comparison of Protein N-Homocysteinylation in Rat Plasma under Elevated Homocysteine Using a Specific Chemical Labeling Method
title Comparison of Protein N-Homocysteinylation in Rat Plasma under Elevated Homocysteine Using a Specific Chemical Labeling Method
title_full Comparison of Protein N-Homocysteinylation in Rat Plasma under Elevated Homocysteine Using a Specific Chemical Labeling Method
title_fullStr Comparison of Protein N-Homocysteinylation in Rat Plasma under Elevated Homocysteine Using a Specific Chemical Labeling Method
title_full_unstemmed Comparison of Protein N-Homocysteinylation in Rat Plasma under Elevated Homocysteine Using a Specific Chemical Labeling Method
title_short Comparison of Protein N-Homocysteinylation in Rat Plasma under Elevated Homocysteine Using a Specific Chemical Labeling Method
title_sort comparison of protein n-homocysteinylation in rat plasma under elevated homocysteine using a specific chemical labeling method
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292613/
https://www.ncbi.nlm.nih.gov/pubmed/27617989
http://dx.doi.org/10.3390/molecules21091195
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