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Interaction of peroxiredoxin V with dihydrolipoamide branched chain transacylase E2 (DBT) in mouse kidney under hypoxia

BACKGROUND: Peroxiredoxin V (Prdx V) plays a major role in preventing oxidative damage as an effective antioxidant protein within a variety of cells through peroxidase activity. However, the function of Prdx V is not limited to peroxidase enzymatic activity per se. It appears to have unique function...

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Autores principales: Ahn, Sun Hee, Yang, Hee-Young, Tran, Gia Buu, Kwon, Joseph, Son, Kyu-Yeol, Kim, Suhee, Dinh, Quoc Thuong, Jung, Seunggon, Lee, Ha-Mi, Cho, Kyoung-Oh, Lee, Tae-Hoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323032/
https://www.ncbi.nlm.nih.gov/pubmed/25670924
http://dx.doi.org/10.1186/s12953-014-0061-2
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author Ahn, Sun Hee
Yang, Hee-Young
Tran, Gia Buu
Kwon, Joseph
Son, Kyu-Yeol
Kim, Suhee
Dinh, Quoc Thuong
Jung, Seunggon
Lee, Ha-Mi
Cho, Kyoung-Oh
Lee, Tae-Hoon
author_facet Ahn, Sun Hee
Yang, Hee-Young
Tran, Gia Buu
Kwon, Joseph
Son, Kyu-Yeol
Kim, Suhee
Dinh, Quoc Thuong
Jung, Seunggon
Lee, Ha-Mi
Cho, Kyoung-Oh
Lee, Tae-Hoon
author_sort Ahn, Sun Hee
collection PubMed
description BACKGROUND: Peroxiredoxin V (Prdx V) plays a major role in preventing oxidative damage as an effective antioxidant protein within a variety of cells through peroxidase activity. However, the function of Prdx V is not limited to peroxidase enzymatic activity per se. It appears to have unique function in regulating cellular response to external stimuli by directing interaction with signaling protein. In this study, we identified Prdx V interacting partners in mouse kidney under hypoxic stress using immunoprecipitation and shotgun proteomic analysis (LC-MS/MS). RESULTS: Immunoprecipitation coupled with nano-UPLC-MS(E) shotgun proteomics was employed to identify putative interacting partners of Prdx V in mouse kidney in the setting of hypoxia. A total of 17 proteins were identified as potential interacting partners of Prdx V by a comparative interactomics analysis in kidney under normoxia versus hypoxia. Dihydrolipoamide branched chain transacylase E2 (DBT) appeared to be a prominent candidate protein displaying enhanced interaction with Prdx V under hypoxic stress. Moreover, hypoxic kidney exhibited altered DBT enzymatic activity compared to normoxia. An enhanced colocalization of these two proteins under hypoxic stress was successfully observed in vitro. Furthermore, peroxidatic cysteine residue (Cys48) of Prdx V is likely to be responsible for interacting with DBT. CONCLUSIONS: We identified several proteins interacting with Prdx V under hypoxic condition known to induce renal oxidative stress. In hypoxic condition, we observed an enhanced interaction of Prdx V and DBT protein as well as increased DBT enzymatic activity. The results from this study will contribute to enhance our understanding of Prdx V’s role in hypoxic stress and may suggest new directions for future research. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12953-014-0061-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-43230322015-02-11 Interaction of peroxiredoxin V with dihydrolipoamide branched chain transacylase E2 (DBT) in mouse kidney under hypoxia Ahn, Sun Hee Yang, Hee-Young Tran, Gia Buu Kwon, Joseph Son, Kyu-Yeol Kim, Suhee Dinh, Quoc Thuong Jung, Seunggon Lee, Ha-Mi Cho, Kyoung-Oh Lee, Tae-Hoon Proteome Sci Research Article BACKGROUND: Peroxiredoxin V (Prdx V) plays a major role in preventing oxidative damage as an effective antioxidant protein within a variety of cells through peroxidase activity. However, the function of Prdx V is not limited to peroxidase enzymatic activity per se. It appears to have unique function in regulating cellular response to external stimuli by directing interaction with signaling protein. In this study, we identified Prdx V interacting partners in mouse kidney under hypoxic stress using immunoprecipitation and shotgun proteomic analysis (LC-MS/MS). RESULTS: Immunoprecipitation coupled with nano-UPLC-MS(E) shotgun proteomics was employed to identify putative interacting partners of Prdx V in mouse kidney in the setting of hypoxia. A total of 17 proteins were identified as potential interacting partners of Prdx V by a comparative interactomics analysis in kidney under normoxia versus hypoxia. Dihydrolipoamide branched chain transacylase E2 (DBT) appeared to be a prominent candidate protein displaying enhanced interaction with Prdx V under hypoxic stress. Moreover, hypoxic kidney exhibited altered DBT enzymatic activity compared to normoxia. An enhanced colocalization of these two proteins under hypoxic stress was successfully observed in vitro. Furthermore, peroxidatic cysteine residue (Cys48) of Prdx V is likely to be responsible for interacting with DBT. CONCLUSIONS: We identified several proteins interacting with Prdx V under hypoxic condition known to induce renal oxidative stress. In hypoxic condition, we observed an enhanced interaction of Prdx V and DBT protein as well as increased DBT enzymatic activity. The results from this study will contribute to enhance our understanding of Prdx V’s role in hypoxic stress and may suggest new directions for future research. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12953-014-0061-2) contains supplementary material, which is available to authorized users. BioMed Central 2015-02-05 /pmc/articles/PMC4323032/ /pubmed/25670924 http://dx.doi.org/10.1186/s12953-014-0061-2 Text en © Ahn et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ahn, Sun Hee
Yang, Hee-Young
Tran, Gia Buu
Kwon, Joseph
Son, Kyu-Yeol
Kim, Suhee
Dinh, Quoc Thuong
Jung, Seunggon
Lee, Ha-Mi
Cho, Kyoung-Oh
Lee, Tae-Hoon
Interaction of peroxiredoxin V with dihydrolipoamide branched chain transacylase E2 (DBT) in mouse kidney under hypoxia
title Interaction of peroxiredoxin V with dihydrolipoamide branched chain transacylase E2 (DBT) in mouse kidney under hypoxia
title_full Interaction of peroxiredoxin V with dihydrolipoamide branched chain transacylase E2 (DBT) in mouse kidney under hypoxia
title_fullStr Interaction of peroxiredoxin V with dihydrolipoamide branched chain transacylase E2 (DBT) in mouse kidney under hypoxia
title_full_unstemmed Interaction of peroxiredoxin V with dihydrolipoamide branched chain transacylase E2 (DBT) in mouse kidney under hypoxia
title_short Interaction of peroxiredoxin V with dihydrolipoamide branched chain transacylase E2 (DBT) in mouse kidney under hypoxia
title_sort interaction of peroxiredoxin v with dihydrolipoamide branched chain transacylase e2 (dbt) in mouse kidney under hypoxia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323032/
https://www.ncbi.nlm.nih.gov/pubmed/25670924
http://dx.doi.org/10.1186/s12953-014-0061-2
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