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Quantitative proteomics in rat saliva stimulated with pilocarpine and isoprenaline
Saliva is increasingly being recognized as a convenient and informative reservoir of proteins that could serve as indicators of various diseases. As the literature remains taciturn with regard to saliva collection methods in rodents, our objective was to provide the protocol for a comprehensive quan...
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Published in: | Archives of oral biology 2025-03, Vol.171, p.106165, Article 106165 |
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creator | Pasternak, Marcin Pogoda, Weronika Ceranowicz, Piotr Cieszkowski, Jakub Madej, Józef Olszanecki, Rafał Suski, Maciej |
description | Saliva is increasingly being recognized as a convenient and informative reservoir of proteins that could serve as indicators of various diseases. As the literature remains taciturn with regard to saliva collection methods in rodents, our objective was to provide the protocol for a comprehensive quantitative proteomic assessment of stimulated rat saliva.
We applied the next-generation proteomic methodology (directDIA) to compare qualitatively and quantitatively stimulated rat saliva specimens obtained from pilocarpine alone and pilocarpine in combination with isoprenaline.
Collectively, we identified 581 protein groups with high confidence across all samples included in the analysis, with the dynamic range of the identifications estimated to cover 5 orders of magnitude difference between the most abundant and least abundant salivary proteins. Our data evidenced that pilocarpine-stimulated saliva collection showed a trend towards more protein groups identified; however, quantitative reproducibility was preferable after dual stimulation.
The main advantage of the double stimulation strategy is the quantitative stability of the salivary proteome, crucial for quantitative salivaomic experiments. We postulate that the latter in combination with the depth of proteome analysis provided by the directDIA technique constitutes a novel analytical tool in research studies designed to unravel the saliva protein composition and its changes in vivo.
•We identified more than 500 proteins in stimulated rat saliva with DIA proteomics.•Identified proteins cover a wide range of functional pathways.•Pilocarpine in combination with isoprenaline provides a more robust salivary proteome. |
doi_str_mv | 10.1016/j.archoralbio.2024.106165 |
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We applied the next-generation proteomic methodology (directDIA) to compare qualitatively and quantitatively stimulated rat saliva specimens obtained from pilocarpine alone and pilocarpine in combination with isoprenaline.
Collectively, we identified 581 protein groups with high confidence across all samples included in the analysis, with the dynamic range of the identifications estimated to cover 5 orders of magnitude difference between the most abundant and least abundant salivary proteins. Our data evidenced that pilocarpine-stimulated saliva collection showed a trend towards more protein groups identified; however, quantitative reproducibility was preferable after dual stimulation.
The main advantage of the double stimulation strategy is the quantitative stability of the salivary proteome, crucial for quantitative salivaomic experiments. We postulate that the latter in combination with the depth of proteome analysis provided by the directDIA technique constitutes a novel analytical tool in research studies designed to unravel the saliva protein composition and its changes in vivo.
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We applied the next-generation proteomic methodology (directDIA) to compare qualitatively and quantitatively stimulated rat saliva specimens obtained from pilocarpine alone and pilocarpine in combination with isoprenaline.
Collectively, we identified 581 protein groups with high confidence across all samples included in the analysis, with the dynamic range of the identifications estimated to cover 5 orders of magnitude difference between the most abundant and least abundant salivary proteins. Our data evidenced that pilocarpine-stimulated saliva collection showed a trend towards more protein groups identified; however, quantitative reproducibility was preferable after dual stimulation.
The main advantage of the double stimulation strategy is the quantitative stability of the salivary proteome, crucial for quantitative salivaomic experiments. We postulate that the latter in combination with the depth of proteome analysis provided by the directDIA technique constitutes a novel analytical tool in research studies designed to unravel the saliva protein composition and its changes in vivo.
•We identified more than 500 proteins in stimulated rat saliva with DIA proteomics.•Identified proteins cover a wide range of functional pathways.•Pilocarpine in combination with isoprenaline provides a more robust salivary proteome.</description><subject>isoprenaline</subject><subject>liquid chromatography-mass spectrometry</subject><subject>pilocarpine</subject><subject>proteomics</subject><subject>saliva</subject><issn>0003-9969</issn><issn>1879-1506</issn><issn>1879-1506</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><recordid>eNqNkE1v1DAQhi0EotvCX0DmxiWL7fgjPqIV0EqVEBWcLceZqLNK4mA7i_rvcbWl4sjJGuuZmXceQt5ztueM64_HvU_hPiY_9Rj3gglZ_zXX6gXZ8c7YhiumX5IdY6xtrNX2glzmfKyl0pq_JhetNUIayXfk7vvml4LFFzwBXVMsEGcMmeJCky80-wlPnuaC8zb5AgP9jeWerjjF4NOKC1C_DBRzXBMsFV7gDXk1-inD26f3ivz88vnH4bq5_fb15vDptgm8pmi6dux4JyXzXsigrazZeqZ6P4DiBoQeRdsFZezQi1Ex45UZpAkjM1YJ4Kq9Ih_Oc2vqXxvk4mbMAabJLxC37FourZJcCVZRe0ZDijknGN2acPbpwXHmHpW6o_tHqXtU6s5Ka--7pzVbP8Pw3PnXYQUOZwDqsSeE5HJAWAIMmCAUN0T8jzV_AH_tjfc</recordid><startdate>202503</startdate><enddate>202503</enddate><creator>Pasternak, Marcin</creator><creator>Pogoda, Weronika</creator><creator>Ceranowicz, Piotr</creator><creator>Cieszkowski, Jakub</creator><creator>Madej, Józef</creator><creator>Olszanecki, Rafał</creator><creator>Suski, Maciej</creator><general>Elsevier Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1082-0590</orcidid><orcidid>https://orcid.org/0000-0001-7575-2184</orcidid></search><sort><creationdate>202503</creationdate><title>Quantitative proteomics in rat saliva stimulated with pilocarpine and isoprenaline</title><author>Pasternak, Marcin ; Pogoda, Weronika ; Ceranowicz, Piotr ; Cieszkowski, Jakub ; Madej, Józef ; Olszanecki, Rafał ; Suski, Maciej</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1661-83f818440aa24c694566b05bade517e26f238c579db2f507a57d47cf07952e153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><topic>isoprenaline</topic><topic>liquid chromatography-mass spectrometry</topic><topic>pilocarpine</topic><topic>proteomics</topic><topic>saliva</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pasternak, Marcin</creatorcontrib><creatorcontrib>Pogoda, Weronika</creatorcontrib><creatorcontrib>Ceranowicz, Piotr</creatorcontrib><creatorcontrib>Cieszkowski, Jakub</creatorcontrib><creatorcontrib>Madej, Józef</creatorcontrib><creatorcontrib>Olszanecki, Rafał</creatorcontrib><creatorcontrib>Suski, Maciej</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of oral biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pasternak, Marcin</au><au>Pogoda, Weronika</au><au>Ceranowicz, Piotr</au><au>Cieszkowski, Jakub</au><au>Madej, Józef</au><au>Olszanecki, Rafał</au><au>Suski, Maciej</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantitative proteomics in rat saliva stimulated with pilocarpine and isoprenaline</atitle><jtitle>Archives of oral biology</jtitle><addtitle>Arch Oral Biol</addtitle><date>2025-03</date><risdate>2025</risdate><volume>171</volume><spage>106165</spage><pages>106165-</pages><artnum>106165</artnum><issn>0003-9969</issn><issn>1879-1506</issn><eissn>1879-1506</eissn><abstract>Saliva is increasingly being recognized as a convenient and informative reservoir of proteins that could serve as indicators of various diseases. As the literature remains taciturn with regard to saliva collection methods in rodents, our objective was to provide the protocol for a comprehensive quantitative proteomic assessment of stimulated rat saliva.
We applied the next-generation proteomic methodology (directDIA) to compare qualitatively and quantitatively stimulated rat saliva specimens obtained from pilocarpine alone and pilocarpine in combination with isoprenaline.
Collectively, we identified 581 protein groups with high confidence across all samples included in the analysis, with the dynamic range of the identifications estimated to cover 5 orders of magnitude difference between the most abundant and least abundant salivary proteins. Our data evidenced that pilocarpine-stimulated saliva collection showed a trend towards more protein groups identified; however, quantitative reproducibility was preferable after dual stimulation.
The main advantage of the double stimulation strategy is the quantitative stability of the salivary proteome, crucial for quantitative salivaomic experiments. We postulate that the latter in combination with the depth of proteome analysis provided by the directDIA technique constitutes a novel analytical tool in research studies designed to unravel the saliva protein composition and its changes in vivo.
•We identified more than 500 proteins in stimulated rat saliva with DIA proteomics.•Identified proteins cover a wide range of functional pathways.•Pilocarpine in combination with isoprenaline provides a more robust salivary proteome.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>39724741</pmid><doi>10.1016/j.archoralbio.2024.106165</doi><orcidid>https://orcid.org/0000-0003-1082-0590</orcidid><orcidid>https://orcid.org/0000-0001-7575-2184</orcidid></addata></record> |
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subjects | isoprenaline liquid chromatography-mass spectrometry pilocarpine proteomics saliva |
title | Quantitative proteomics in rat saliva stimulated with pilocarpine and isoprenaline |
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