Optimized Workflow for Selecting Peptides for HDX-MS Data Analyses
Hydrogen deuterium exchange measured by mass spectrometry (HDX-MS) is a commonly used technique for studying the structural dynamics of proteins in solution. The first part of any bottom-up HDX-MS experiment is to identify the peptides generated from a digestion step. This requires manual inspection...
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Veröffentlicht in: | Journal of the American Society for Mass Spectrometry 2018-11, Vol.29 (11), p.2278-2281 |
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description | Hydrogen deuterium exchange measured by mass spectrometry (HDX-MS) is a commonly used technique for studying the structural dynamics of proteins in solution. The first part of any bottom-up HDX-MS experiment is to identify the peptides generated from a digestion step. This requires manual inspection of the identified peptides to determine their use for HDX-MS analysis, which is a time-consuming task. Throughout the literature, there have been different approaches for removing peptides that do not yield quantifiable HDX information. This includes using validity scores from the software used in the generation of the peptide map and that the peptide should be found in two out of three technical replicate experiments. Here, we analyze the previously available methods for filtering the identified peptides in regard to their ability to predict whether a peptide will provide quantifiable HDX-MS data or not. We also present a new score-based system relying on a combination of MS/MS parameters that offers an improved method for separating quantifiable peptides from the nonquantifiable. Using this score-based method reduces the number of peptide spectra that needs to be manually inspected and thereby the time spent curating HDX-MS data.
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doi_str_mv | 10.1007/s13361-018-2056-1 |
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Graphical Abstract
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Graphical Abstract
ᅟ</description><subject>Analytical Chemistry</subject><subject>Application Note</subject><subject>Bioinformatics</subject><subject>Biotechnology</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Deuterium</subject><subject>Dynamic structural analysis</subject><subject>Filtration</subject><subject>Identification methods</subject><subject>Inspection</subject><subject>Mass spectrometry</subject><subject>Organic Chemistry</subject><subject>Peptides</subject><subject>Proteins</subject><subject>Proteomics</subject><subject>Workflow</subject><issn>1044-0305</issn><issn>1879-1123</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp1kE1P3DAQhi3Uiq_yA7igSL30YpixE9s58lE-JCqQtlW5WY4zRqHZzdbOqoJfj3cXqITEySPPM--MHsb2EQ4RQB8llFIhBzRcQKU4brBtNLrmiEJ-yjWUJQcJ1RbbSekBADXUepNtyVxhWcI2O7mZj920e6K2-D3EP6Ef_hVhiMWEevJjN7svbikTLaXV9-XZHf8xKc7c6IrjmesfE6Uv7HNwfaK9l3eX_Tr__vP0kl_fXFydHl9zL7UYeVMrr5yuhPe-MoSgG2egCZ5qLaqggJRvUVVQSmUECtMoCrJxoQ2alAC5y76tc-dx-LugNNpplzz1vZvRsEhWQG20llgv0a_v0IdhEfO9K0qbsjR1mSlcUz4OKUUKdh67qYuPFsEuBdu1YJsF26Vgi3nm4CV50UypfZt4NZoBsQZSbs3uKf5f_XHqM8J-g6k</recordid><startdate>20181101</startdate><enddate>20181101</enddate><creator>Sørensen, Lars</creator><creator>Salbo, Rune</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FG</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>P5Z</scope><scope>P62</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7653-4920</orcidid></search><sort><creationdate>20181101</creationdate><title>Optimized Workflow for Selecting Peptides for HDX-MS Data Analyses</title><author>Sørensen, Lars ; 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Am. Soc. Mass Spectrom</stitle><addtitle>J Am Soc Mass Spectrom</addtitle><date>2018-11-01</date><risdate>2018</risdate><volume>29</volume><issue>11</issue><spage>2278</spage><epage>2281</epage><pages>2278-2281</pages><issn>1044-0305</issn><eissn>1879-1123</eissn><abstract>Hydrogen deuterium exchange measured by mass spectrometry (HDX-MS) is a commonly used technique for studying the structural dynamics of proteins in solution. The first part of any bottom-up HDX-MS experiment is to identify the peptides generated from a digestion step. This requires manual inspection of the identified peptides to determine their use for HDX-MS analysis, which is a time-consuming task. Throughout the literature, there have been different approaches for removing peptides that do not yield quantifiable HDX information. This includes using validity scores from the software used in the generation of the peptide map and that the peptide should be found in two out of three technical replicate experiments. 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subjects | Analytical Chemistry Application Note Bioinformatics Biotechnology Chemistry Chemistry and Materials Science Deuterium Dynamic structural analysis Filtration Identification methods Inspection Mass spectrometry Organic Chemistry Peptides Proteins Proteomics Workflow |
title | Optimized Workflow for Selecting Peptides for HDX-MS Data Analyses |
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