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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...
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Published in: | Journal of proteomics 2024-01, Vol.290, p.105034, Article 105034 |
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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 |
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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.
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•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 < 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 < 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> |
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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 |
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