Loading…

Quantitative serum proteome analysis using tandem mass tags in dogs with epilepsy

This study included four groups of dogs (group A: healthy controls, group B: idiopathic epilepsy receiving antiepileptic medication (AEM), group C: idiopathic epilepsy without AEM, group D: structural epilepsy). Comparative quantitative proteomic analysis of serum samples among the groups was the ma...

Full description

Saved in:
Bibliographic Details
Published in:Journal of proteomics 2024-01, Vol.290, p.105034, Article 105034
Main Authors: Baka, Rania D., Kuleš, Josipa, Beletić, Anđelo, Farkaš, Vladimir, RešetarMaslov, Dina, Ljubić, Blanka Beer, Rubić, Ivana, Mrljak, Vladimir, McLaughlin, Marκ, Eckersall, David, Polizopoulou, Zoe
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c359t-4dc117a84118fc2f5749e09a7c46594b46a3ba148d4426aec9e735692b4166ae3
cites cdi_FETCH-LOGICAL-c359t-4dc117a84118fc2f5749e09a7c46594b46a3ba148d4426aec9e735692b4166ae3
container_end_page
container_issue
container_start_page 105034
container_title Journal of proteomics
container_volume 290
creator Baka, Rania D.
Kuleš, Josipa
Beletić, Anđelo
Farkaš, Vladimir
RešetarMaslov, Dina
Ljubić, Blanka Beer
Rubić, Ivana
Mrljak, Vladimir
McLaughlin, Marκ
Eckersall, David
Polizopoulou, Zoe
description This study included four groups of dogs (group A: healthy controls, group B: idiopathic epilepsy receiving antiepileptic medication (AEM), group C: idiopathic epilepsy without AEM, group D: structural epilepsy). Comparative quantitative proteomic analysis of serum samples among the groups was the main target of the study. Samples were analyzed by a quantitative Tandem-Mass-Tags approach on the Q-Exactive-Plus Hybrid Quadrupole-Orbitrap mass-spectrometer. Identification and relative quantification were performed in Proteome Discoverer. Data were analyzed using R. Gene ontology terms were analyzed based on Canis lupus familiaris database. Data are available via ProteomeXchange with identifier PXD041129. Eighty-one proteins with different relative adundance were identified in the four groups and 25 were master proteins (p 
doi_str_mv 10.1016/j.jprot.2023.105034
format article
fullrecord <record><control><sourceid>elsevier_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1016_j_jprot_2023_105034</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1874391923002233</els_id><sourcerecordid>S1874391923002233</sourcerecordid><originalsourceid>FETCH-LOGICAL-c359t-4dc117a84118fc2f5749e09a7c46594b46a3ba148d4426aec9e735692b4166ae3</originalsourceid><addsrcrecordid>eNp9kMtOwzAQRb0AiVL4Ajb-gRQ7dux4wQJVvKRKqBKsLceZFEd5yeMW9e9JKWtWd-ZKZzQ6hNxxtuKMq_t21U5xTKuc5WJuCibkBVnwUstMGG6uyDViy5ji2ugF2W73bkghuRQOQBHivqcnHMYeqBtcd8SAdI9h2NHkhhp62jvEed4hDQOtxzm_Q_qiMIUOJjzekMvGdQi3f7kkn89PH-vXbPP-8rZ-3GReFCZlsvaca1dKzsvG502hpQFmnPZSFUZWUjlROS7LWspcOfAGtCiUySvJ1byLJRHnuz6OiBEaO8XQu3i0nNmTCdvaXxP2ZMKeTczUw5mC-bVDgGjRBxg81CGCT7Yew7_8DwvBa24</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Quantitative serum proteome analysis using tandem mass tags in dogs with epilepsy</title><source>ScienceDirect Journals</source><creator>Baka, Rania D. ; Kuleš, Josipa ; Beletić, Anđelo ; Farkaš, Vladimir ; RešetarMaslov, Dina ; Ljubić, Blanka Beer ; Rubić, Ivana ; Mrljak, Vladimir ; McLaughlin, Marκ ; Eckersall, David ; Polizopoulou, Zoe</creator><creatorcontrib>Baka, Rania D. ; Kuleš, Josipa ; Beletić, Anđelo ; Farkaš, Vladimir ; RešetarMaslov, Dina ; Ljubić, Blanka Beer ; Rubić, Ivana ; Mrljak, Vladimir ; McLaughlin, Marκ ; Eckersall, David ; Polizopoulou, Zoe</creatorcontrib><description>This study included four groups of dogs (group A: healthy controls, group B: idiopathic epilepsy receiving antiepileptic medication (AEM), group C: idiopathic epilepsy without AEM, group D: structural epilepsy). Comparative quantitative proteomic analysis of serum samples among the groups was the main target of the study. Samples were analyzed by a quantitative Tandem-Mass-Tags approach on the Q-Exactive-Plus Hybrid Quadrupole-Orbitrap mass-spectrometer. Identification and relative quantification were performed in Proteome Discoverer. Data were analyzed using R. Gene ontology terms were analyzed based on Canis lupus familiaris database. Data are available via ProteomeXchange with identifier PXD041129. Eighty-one proteins with different relative adundance were identified in the four groups and 25 were master proteins (p &lt; 0.05). Clusterin (CLU), and apolipoprotein A1 (APOA1) had higher abundance in the three groups of dogs (groups B, C, D) compared to controls. Amine oxidase (AOC3) was higher in abundance in group B compared to groups C and D, and lower in group A. Adiponectin (ADIPOQ) had higher abundance in groups C compared to group A. ADIPOQ and fibronectin (FN1) had higher abundance in group B compared to group C and D. Peroxidase activity assay was used to quantify HP abundance change, validating and correlating with proteomic analysis (r = 0.8796). The proteomic analysis of serum samples from epileptic dogs indicated potential markers of epilepsy (CLU), proteins that may contribute to nerve tissue regeneration (APOA1), and contributing factors to epileptogenesis (AOC3). AEM could alter extracellular matrix proteins (FN1). Illness (epilepsy) severity could influence ADIPOQ abundance. [Display omitted] •Serum proteome profile significantly differed between epileptic and healthy dogs.•Haptoglobin abundance changes correlated with peroxidase activity assay results.•Serum clusterin abundance changes may indicate its prognostic role in epilepsy.•Serum apolipoprotein A1 and amine oxidase changes may contribute to epileptogenesis.•Serum fibronectin abundance change may be altered by antiepileptic medication.</description><identifier>ISSN: 1874-3919</identifier><identifier>DOI: 10.1016/j.jprot.2023.105034</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Dog ; Haptoglobin binding assay ; Idiopathic epilepsy ; Serum ; Specific ELISA assay ; TMT-based proteomics</subject><ispartof>Journal of proteomics, 2024-01, Vol.290, p.105034, Article 105034</ispartof><rights>2023</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-4dc117a84118fc2f5749e09a7c46594b46a3ba148d4426aec9e735692b4166ae3</citedby><cites>FETCH-LOGICAL-c359t-4dc117a84118fc2f5749e09a7c46594b46a3ba148d4426aec9e735692b4166ae3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Baka, Rania D.</creatorcontrib><creatorcontrib>Kuleš, Josipa</creatorcontrib><creatorcontrib>Beletić, Anđelo</creatorcontrib><creatorcontrib>Farkaš, Vladimir</creatorcontrib><creatorcontrib>RešetarMaslov, Dina</creatorcontrib><creatorcontrib>Ljubić, Blanka Beer</creatorcontrib><creatorcontrib>Rubić, Ivana</creatorcontrib><creatorcontrib>Mrljak, Vladimir</creatorcontrib><creatorcontrib>McLaughlin, Marκ</creatorcontrib><creatorcontrib>Eckersall, David</creatorcontrib><creatorcontrib>Polizopoulou, Zoe</creatorcontrib><title>Quantitative serum proteome analysis using tandem mass tags in dogs with epilepsy</title><title>Journal of proteomics</title><description>This study included four groups of dogs (group A: healthy controls, group B: idiopathic epilepsy receiving antiepileptic medication (AEM), group C: idiopathic epilepsy without AEM, group D: structural epilepsy). Comparative quantitative proteomic analysis of serum samples among the groups was the main target of the study. Samples were analyzed by a quantitative Tandem-Mass-Tags approach on the Q-Exactive-Plus Hybrid Quadrupole-Orbitrap mass-spectrometer. Identification and relative quantification were performed in Proteome Discoverer. Data were analyzed using R. Gene ontology terms were analyzed based on Canis lupus familiaris database. Data are available via ProteomeXchange with identifier PXD041129. Eighty-one proteins with different relative adundance were identified in the four groups and 25 were master proteins (p &lt; 0.05). Clusterin (CLU), and apolipoprotein A1 (APOA1) had higher abundance in the three groups of dogs (groups B, C, D) compared to controls. Amine oxidase (AOC3) was higher in abundance in group B compared to groups C and D, and lower in group A. Adiponectin (ADIPOQ) had higher abundance in groups C compared to group A. ADIPOQ and fibronectin (FN1) had higher abundance in group B compared to group C and D. Peroxidase activity assay was used to quantify HP abundance change, validating and correlating with proteomic analysis (r = 0.8796). The proteomic analysis of serum samples from epileptic dogs indicated potential markers of epilepsy (CLU), proteins that may contribute to nerve tissue regeneration (APOA1), and contributing factors to epileptogenesis (AOC3). AEM could alter extracellular matrix proteins (FN1). Illness (epilepsy) severity could influence ADIPOQ abundance. [Display omitted] •Serum proteome profile significantly differed between epileptic and healthy dogs.•Haptoglobin abundance changes correlated with peroxidase activity assay results.•Serum clusterin abundance changes may indicate its prognostic role in epilepsy.•Serum apolipoprotein A1 and amine oxidase changes may contribute to epileptogenesis.•Serum fibronectin abundance change may be altered by antiepileptic medication.</description><subject>Dog</subject><subject>Haptoglobin binding assay</subject><subject>Idiopathic epilepsy</subject><subject>Serum</subject><subject>Specific ELISA assay</subject><subject>TMT-based proteomics</subject><issn>1874-3919</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kMtOwzAQRb0AiVL4Ajb-gRQ7dux4wQJVvKRKqBKsLceZFEd5yeMW9e9JKWtWd-ZKZzQ6hNxxtuKMq_t21U5xTKuc5WJuCibkBVnwUstMGG6uyDViy5ji2ugF2W73bkghuRQOQBHivqcnHMYeqBtcd8SAdI9h2NHkhhp62jvEed4hDQOtxzm_Q_qiMIUOJjzekMvGdQi3f7kkn89PH-vXbPP-8rZ-3GReFCZlsvaca1dKzsvG502hpQFmnPZSFUZWUjlROS7LWspcOfAGtCiUySvJ1byLJRHnuz6OiBEaO8XQu3i0nNmTCdvaXxP2ZMKeTczUw5mC-bVDgGjRBxg81CGCT7Yew7_8DwvBa24</recordid><startdate>20240106</startdate><enddate>20240106</enddate><creator>Baka, Rania D.</creator><creator>Kuleš, Josipa</creator><creator>Beletić, Anđelo</creator><creator>Farkaš, Vladimir</creator><creator>RešetarMaslov, Dina</creator><creator>Ljubić, Blanka Beer</creator><creator>Rubić, Ivana</creator><creator>Mrljak, Vladimir</creator><creator>McLaughlin, Marκ</creator><creator>Eckersall, David</creator><creator>Polizopoulou, Zoe</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20240106</creationdate><title>Quantitative serum proteome analysis using tandem mass tags in dogs with epilepsy</title><author>Baka, Rania D. ; Kuleš, Josipa ; Beletić, Anđelo ; Farkaš, Vladimir ; RešetarMaslov, Dina ; Ljubić, Blanka Beer ; Rubić, Ivana ; Mrljak, Vladimir ; McLaughlin, Marκ ; Eckersall, David ; Polizopoulou, Zoe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-4dc117a84118fc2f5749e09a7c46594b46a3ba148d4426aec9e735692b4166ae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Dog</topic><topic>Haptoglobin binding assay</topic><topic>Idiopathic epilepsy</topic><topic>Serum</topic><topic>Specific ELISA assay</topic><topic>TMT-based proteomics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baka, Rania D.</creatorcontrib><creatorcontrib>Kuleš, Josipa</creatorcontrib><creatorcontrib>Beletić, Anđelo</creatorcontrib><creatorcontrib>Farkaš, Vladimir</creatorcontrib><creatorcontrib>RešetarMaslov, Dina</creatorcontrib><creatorcontrib>Ljubić, Blanka Beer</creatorcontrib><creatorcontrib>Rubić, Ivana</creatorcontrib><creatorcontrib>Mrljak, Vladimir</creatorcontrib><creatorcontrib>McLaughlin, Marκ</creatorcontrib><creatorcontrib>Eckersall, David</creatorcontrib><creatorcontrib>Polizopoulou, Zoe</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of proteomics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baka, Rania D.</au><au>Kuleš, Josipa</au><au>Beletić, Anđelo</au><au>Farkaš, Vladimir</au><au>RešetarMaslov, Dina</au><au>Ljubić, Blanka Beer</au><au>Rubić, Ivana</au><au>Mrljak, Vladimir</au><au>McLaughlin, Marκ</au><au>Eckersall, David</au><au>Polizopoulou, Zoe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantitative serum proteome analysis using tandem mass tags in dogs with epilepsy</atitle><jtitle>Journal of proteomics</jtitle><date>2024-01-06</date><risdate>2024</risdate><volume>290</volume><spage>105034</spage><pages>105034-</pages><artnum>105034</artnum><issn>1874-3919</issn><abstract>This study included four groups of dogs (group A: healthy controls, group B: idiopathic epilepsy receiving antiepileptic medication (AEM), group C: idiopathic epilepsy without AEM, group D: structural epilepsy). Comparative quantitative proteomic analysis of serum samples among the groups was the main target of the study. Samples were analyzed by a quantitative Tandem-Mass-Tags approach on the Q-Exactive-Plus Hybrid Quadrupole-Orbitrap mass-spectrometer. Identification and relative quantification were performed in Proteome Discoverer. Data were analyzed using R. Gene ontology terms were analyzed based on Canis lupus familiaris database. Data are available via ProteomeXchange with identifier PXD041129. Eighty-one proteins with different relative adundance were identified in the four groups and 25 were master proteins (p &lt; 0.05). Clusterin (CLU), and apolipoprotein A1 (APOA1) had higher abundance in the three groups of dogs (groups B, C, D) compared to controls. Amine oxidase (AOC3) was higher in abundance in group B compared to groups C and D, and lower in group A. Adiponectin (ADIPOQ) had higher abundance in groups C compared to group A. ADIPOQ and fibronectin (FN1) had higher abundance in group B compared to group C and D. Peroxidase activity assay was used to quantify HP abundance change, validating and correlating with proteomic analysis (r = 0.8796). The proteomic analysis of serum samples from epileptic dogs indicated potential markers of epilepsy (CLU), proteins that may contribute to nerve tissue regeneration (APOA1), and contributing factors to epileptogenesis (AOC3). AEM could alter extracellular matrix proteins (FN1). Illness (epilepsy) severity could influence ADIPOQ abundance. [Display omitted] •Serum proteome profile significantly differed between epileptic and healthy dogs.•Haptoglobin abundance changes correlated with peroxidase activity assay results.•Serum clusterin abundance changes may indicate its prognostic role in epilepsy.•Serum apolipoprotein A1 and amine oxidase changes may contribute to epileptogenesis.•Serum fibronectin abundance change may be altered by antiepileptic medication.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.jprot.2023.105034</doi></addata></record>
fulltext fulltext
identifier ISSN: 1874-3919
ispartof Journal of proteomics, 2024-01, Vol.290, p.105034, Article 105034
issn 1874-3919
language eng
recordid cdi_crossref_primary_10_1016_j_jprot_2023_105034
source ScienceDirect Journals
subjects Dog
Haptoglobin binding assay
Idiopathic epilepsy
Serum
Specific ELISA assay
TMT-based proteomics
title Quantitative serum proteome analysis using tandem mass tags in dogs with epilepsy
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T14%3A49%3A37IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Quantitative%20serum%20proteome%20analysis%20using%20tandem%20mass%20tags%20in%20dogs%20with%20epilepsy&rft.jtitle=Journal%20of%20proteomics&rft.au=Baka,%20Rania%20D.&rft.date=2024-01-06&rft.volume=290&rft.spage=105034&rft.pages=105034-&rft.artnum=105034&rft.issn=1874-3919&rft_id=info:doi/10.1016/j.jprot.2023.105034&rft_dat=%3Celsevier_cross%3ES1874391923002233%3C/elsevier_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c359t-4dc117a84118fc2f5749e09a7c46594b46a3ba148d4426aec9e735692b4166ae3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true