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Protocol for Increasing the Sensitivity of MS-Based Protein Detection in Human Chorionic Villi
An important step in the proteomic analysis of missing proteins is the use of a wide range of tissues, optimal extraction, and the processing of protein material in order to ensure the highest sensitivity in downstream protein detection. This work describes a purification protocol for identifying lo...
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Published in: | Current issues in molecular biology 2022-05, Vol.44 (5), p.2069-2088 |
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creator | Shkrigunov, Timur Pogodin, Pavel Zgoda, Victor Larina, Olesya Kisrieva, Yulia Klimenko, Maria Latyshkevich, Oleg Klimenko, Peter Lisitsa, Andrey Petushkova, Natalia |
description | An important step in the proteomic analysis of missing proteins is the use of a wide range of tissues, optimal extraction, and the processing of protein material in order to ensure the highest sensitivity in downstream protein detection. This work describes a purification protocol for identifying low-abundance proteins in human chorionic villi using the proposed "1DE-gel concentration" method. This involves the removal of SDS in a short electrophoresis run in a stacking gel without protein separation. Following the in-gel digestion of the obtained holistic single protein band, we used the peptide mixture for further LC-MS/MS analysis. Statistically significant results were derived from six datasets, containing three treatments, each from two tissue sources (elective or missed abortions). The 1DE-gel concentration increased the coverage of the chorionic villus proteome. Our approach allowed the identification of 15 low-abundance proteins, of which some had not been previously detected via the mass spectrometry of trophoblasts. In the post hoc data analysis, we found a dubious or uncertain protein (PSG7) encoded on human chromosome 19 according to neXtProt. A proteomic sample preparation workflow with the 1DE-gel concentration can be used as a prospective tool for uncovering the low-abundance part of the human proteome. |
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This work describes a purification protocol for identifying low-abundance proteins in human chorionic villi using the proposed "1DE-gel concentration" method. This involves the removal of SDS in a short electrophoresis run in a stacking gel without protein separation. Following the in-gel digestion of the obtained holistic single protein band, we used the peptide mixture for further LC-MS/MS analysis. Statistically significant results were derived from six datasets, containing three treatments, each from two tissue sources (elective or missed abortions). The 1DE-gel concentration increased the coverage of the chorionic villus proteome. Our approach allowed the identification of 15 low-abundance proteins, of which some had not been previously detected via the mass spectrometry of trophoblasts. In the post hoc data analysis, we found a dubious or uncertain protein (PSG7) encoded on human chromosome 19 according to neXtProt. A proteomic sample preparation workflow with the 1DE-gel concentration can be used as a prospective tool for uncovering the low-abundance part of the human proteome.</description><identifier>ISSN: 1467-3045</identifier><identifier>ISSN: 1467-3037</identifier><identifier>EISSN: 1467-3045</identifier><identifier>DOI: 10.3390/cimb44050140</identifier><identifier>PMID: 35678669</identifier><language>eng</language><publisher>Switzerland: MDPI</publisher><subject>1DE-gel concentration ; chorionic villi ; elective abortion ; LC–MS/MS ; low-abundance proteins ; SDS extracts</subject><ispartof>Current issues in molecular biology, 2022-05, Vol.44 (5), p.2069-2088</ispartof><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c380t-8b24b7b43cca2e8ad8f9a7a5106e55d833d1881adc2b17f3f1076c5ec33eb2653</citedby><cites>FETCH-LOGICAL-c380t-8b24b7b43cca2e8ad8f9a7a5106e55d833d1881adc2b17f3f1076c5ec33eb2653</cites><orcidid>0000-0003-1843-7668 ; 0000-0002-4101-4607 ; 0000-0002-4448-7629 ; 0000-0002-4532-4274</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164042/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164042/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35678669$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shkrigunov, Timur</creatorcontrib><creatorcontrib>Pogodin, Pavel</creatorcontrib><creatorcontrib>Zgoda, Victor</creatorcontrib><creatorcontrib>Larina, Olesya</creatorcontrib><creatorcontrib>Kisrieva, Yulia</creatorcontrib><creatorcontrib>Klimenko, Maria</creatorcontrib><creatorcontrib>Latyshkevich, Oleg</creatorcontrib><creatorcontrib>Klimenko, Peter</creatorcontrib><creatorcontrib>Lisitsa, Andrey</creatorcontrib><creatorcontrib>Petushkova, Natalia</creatorcontrib><title>Protocol for Increasing the Sensitivity of MS-Based Protein Detection in Human Chorionic Villi</title><title>Current issues in molecular biology</title><addtitle>Curr Issues Mol Biol</addtitle><description>An important step in the proteomic analysis of missing proteins is the use of a wide range of tissues, optimal extraction, and the processing of protein material in order to ensure the highest sensitivity in downstream protein detection. 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This work describes a purification protocol for identifying low-abundance proteins in human chorionic villi using the proposed "1DE-gel concentration" method. This involves the removal of SDS in a short electrophoresis run in a stacking gel without protein separation. Following the in-gel digestion of the obtained holistic single protein band, we used the peptide mixture for further LC-MS/MS analysis. Statistically significant results were derived from six datasets, containing three treatments, each from two tissue sources (elective or missed abortions). The 1DE-gel concentration increased the coverage of the chorionic villus proteome. Our approach allowed the identification of 15 low-abundance proteins, of which some had not been previously detected via the mass spectrometry of trophoblasts. In the post hoc data analysis, we found a dubious or uncertain protein (PSG7) encoded on human chromosome 19 according to neXtProt. 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subjects | 1DE-gel concentration chorionic villi elective abortion LC–MS/MS low-abundance proteins SDS extracts |
title | Protocol for Increasing the Sensitivity of MS-Based Protein Detection in Human Chorionic Villi |
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