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Dataset of quantitative proteomic analysis to understand aging processes in rabbit liver

Here, we present a proteomics dataset of liver proteins to understand aging in rabbits, which complements the publication “Quantitative proteomics to study aging in rabbit liver” [1]. This dataset was generated to understand the molecular basis and metabolic changes of aging processes in liver, whic...

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Autores principales: Amin, Bushra, Robinson, Renã A.S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7262418/
https://www.ncbi.nlm.nih.gov/pubmed/32490075
http://dx.doi.org/10.1016/j.dib.2020.105701
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author Amin, Bushra
Robinson, Renã A.S.
author_facet Amin, Bushra
Robinson, Renã A.S.
author_sort Amin, Bushra
collection PubMed
description Here, we present a proteomics dataset of liver proteins to understand aging in rabbits, which complements the publication “Quantitative proteomics to study aging in rabbit liver” [1]. This dataset was generated to understand the molecular basis and metabolic changes of aging processes in liver, which is the main organ involved in metabolism, detoxification, transport, and signaling. Proteins from young, middle, and old age rabbits were extracted and digested. Generated peptides were labeled with light or heavy dimethyl groups at their N-termini, while lysine amines were labeled with TMT10-plex using a cPILOT workflow [2]. Labeled peptides were fractionated by basic pH reverse phase chromatography and analyzed with online reverse phase LC coupled with tandem mass spectrometry (MS/MS and MS(3)). The RAW files were generated using a Fusion Lumos Orbitrap mass spectrometer (Thermo Scientific) and processed with Proteome Discoverer (PD) version 2.2 to generate a list of identified and quantified proteins. Data was searched against the Rabbit UniProtKB redundant database. A total of 3,867 proteins were identified corresponding to 2,586 protein groups and 22,229 peptides. Dynamic levels of age-related proteins associated with fat metabolism, mitochondrial dysfunction, and protein degradation were detected. The mass spectrometry proteomics data (RAW files) and processed Proteome Discoverer 2.2 files (MSF files) have been deposited to the Proteomics Identification Database (PRIDE) ProteomeXchange Consortium and can be accessed with the dataset identifier PDX013220 (http://www.ebi.ac.uk/pride/archive/projects/PXD013220).
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spelling pubmed-72624182020-06-01 Dataset of quantitative proteomic analysis to understand aging processes in rabbit liver Amin, Bushra Robinson, Renã A.S. Data Brief Biochemistry, Genetics and Molecular Biology Here, we present a proteomics dataset of liver proteins to understand aging in rabbits, which complements the publication “Quantitative proteomics to study aging in rabbit liver” [1]. This dataset was generated to understand the molecular basis and metabolic changes of aging processes in liver, which is the main organ involved in metabolism, detoxification, transport, and signaling. Proteins from young, middle, and old age rabbits were extracted and digested. Generated peptides were labeled with light or heavy dimethyl groups at their N-termini, while lysine amines were labeled with TMT10-plex using a cPILOT workflow [2]. Labeled peptides were fractionated by basic pH reverse phase chromatography and analyzed with online reverse phase LC coupled with tandem mass spectrometry (MS/MS and MS(3)). The RAW files were generated using a Fusion Lumos Orbitrap mass spectrometer (Thermo Scientific) and processed with Proteome Discoverer (PD) version 2.2 to generate a list of identified and quantified proteins. Data was searched against the Rabbit UniProtKB redundant database. A total of 3,867 proteins were identified corresponding to 2,586 protein groups and 22,229 peptides. Dynamic levels of age-related proteins associated with fat metabolism, mitochondrial dysfunction, and protein degradation were detected. The mass spectrometry proteomics data (RAW files) and processed Proteome Discoverer 2.2 files (MSF files) have been deposited to the Proteomics Identification Database (PRIDE) ProteomeXchange Consortium and can be accessed with the dataset identifier PDX013220 (http://www.ebi.ac.uk/pride/archive/projects/PXD013220). Elsevier 2020-05-15 /pmc/articles/PMC7262418/ /pubmed/32490075 http://dx.doi.org/10.1016/j.dib.2020.105701 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Biochemistry, Genetics and Molecular Biology
Amin, Bushra
Robinson, Renã A.S.
Dataset of quantitative proteomic analysis to understand aging processes in rabbit liver
title Dataset of quantitative proteomic analysis to understand aging processes in rabbit liver
title_full Dataset of quantitative proteomic analysis to understand aging processes in rabbit liver
title_fullStr Dataset of quantitative proteomic analysis to understand aging processes in rabbit liver
title_full_unstemmed Dataset of quantitative proteomic analysis to understand aging processes in rabbit liver
title_short Dataset of quantitative proteomic analysis to understand aging processes in rabbit liver
title_sort dataset of quantitative proteomic analysis to understand aging processes in rabbit liver
topic Biochemistry, Genetics and Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7262418/
https://www.ncbi.nlm.nih.gov/pubmed/32490075
http://dx.doi.org/10.1016/j.dib.2020.105701
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