Comparative quantitative LC–MS/MS analysis of 13 amylase/trypsin inhibitors in ancient and modern Triticum species
Amylase/trypsin inhibitors (ATIs) are major wheat allergens and they are also implicated in causing non-celiac gluten sensitivity and worsening other inflammatory conditions. With only few studies on ATI contents in different Triticum species available so far, we developed a targeted liquid chromato...
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description | Amylase/trypsin inhibitors (ATIs) are major wheat allergens and they are also implicated in causing non-celiac gluten sensitivity and worsening other inflammatory conditions. With only few studies on ATI contents in different
Triticum
species available so far, we developed a targeted liquid chromatography-tandem mass spectrometry (LC–MS/MS) method based on stable isotope dilution assays to quantitate the 13 most important ATIs in a well-defined sample set of eight cultivars of common wheat and durum wheat (modern species), as well as spelt, emmer and einkorn (ancient species) grown at three locations in Germany, respectively. Only few ATIs with low contents were detected in einkorn. In contrast, spelt had the highest total ATI contents. Emmer and common wheat had similar total ATI contents, with durum wheat having lower contents than common wheat. Due to the lack of correlation, it was not possible to estimate ATI contents based on crude protein contents. The wheat species had a higher influence on ATI contents than the growing location and the heritability of this trait was high. Despite comparatively low intra-species variability, some cultivars were identified that may be promising candidates for breeding for naturally low ATI contents. |
doi_str_mv | 10.1038/s41598-020-71413-z |
format | Article |
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Triticum
species available so far, we developed a targeted liquid chromatography-tandem mass spectrometry (LC–MS/MS) method based on stable isotope dilution assays to quantitate the 13 most important ATIs in a well-defined sample set of eight cultivars of common wheat and durum wheat (modern species), as well as spelt, emmer and einkorn (ancient species) grown at three locations in Germany, respectively. Only few ATIs with low contents were detected in einkorn. In contrast, spelt had the highest total ATI contents. Emmer and common wheat had similar total ATI contents, with durum wheat having lower contents than common wheat. Due to the lack of correlation, it was not possible to estimate ATI contents based on crude protein contents. The wheat species had a higher influence on ATI contents than the growing location and the heritability of this trait was high. Despite comparatively low intra-species variability, some cultivars were identified that may be promising candidates for breeding for naturally low ATI contents.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-020-71413-z</identifier><identifier>PMID: 32883982</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/449/1870 ; 639/638/11/296 ; 639/638/45/475 ; 639/638/45/612 ; Action potential ; Amylases - antagonists & inhibitors ; Amylases - classification ; Arrhythmia ; Cardiac arrhythmia ; Cardiomyocytes ; Chromatography, Liquid - methods ; Cultivars ; Drug discovery ; Germany ; Glucocorticoids ; Gluten ; Heart ; Heart diseases ; Humanities and Social Sciences ; Liquid chromatography ; Long QT syndrome ; Mass spectrometry ; multidisciplinary ; Phosphorylation ; Plant Proteins - analysis ; Pluripotency ; Prostate cancer ; Science ; Science (multidisciplinary) ; Sodium channels (voltage-gated) ; Stable isotopes ; Stem cells ; Tandem Mass Spectrometry - methods ; Triticum - growth & development ; Triticum - metabolism ; Trypsin - chemistry ; Trypsin Inhibitors - analysis ; Wheat</subject><ispartof>Scientific reports, 2020-09, Vol.10 (1), p.14570-14570, Article 14570</ispartof><rights>The Author(s) 2020</rights><rights>The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-34922bfda79b7ab1dfb423d0a1bdf0aceb71f74119c115d3b70e7a39736649fc3</citedby><cites>FETCH-LOGICAL-c511t-34922bfda79b7ab1dfb423d0a1bdf0aceb71f74119c115d3b70e7a39736649fc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7471314/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7471314/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,41120,42189,51576,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32883982$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Geisslitz, Sabrina</creatorcontrib><creatorcontrib>Longin, C. Friedrich H.</creatorcontrib><creatorcontrib>Koehler, Peter</creatorcontrib><creatorcontrib>Scherf, Katharina Anne</creatorcontrib><title>Comparative quantitative LC–MS/MS analysis of 13 amylase/trypsin inhibitors in ancient and modern Triticum species</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Amylase/trypsin inhibitors (ATIs) are major wheat allergens and they are also implicated in causing non-celiac gluten sensitivity and worsening other inflammatory conditions. With only few studies on ATI contents in different
Triticum
species available so far, we developed a targeted liquid chromatography-tandem mass spectrometry (LC–MS/MS) method based on stable isotope dilution assays to quantitate the 13 most important ATIs in a well-defined sample set of eight cultivars of common wheat and durum wheat (modern species), as well as spelt, emmer and einkorn (ancient species) grown at three locations in Germany, respectively. Only few ATIs with low contents were detected in einkorn. In contrast, spelt had the highest total ATI contents. Emmer and common wheat had similar total ATI contents, with durum wheat having lower contents than common wheat. Due to the lack of correlation, it was not possible to estimate ATI contents based on crude protein contents. The wheat species had a higher influence on ATI contents than the growing location and the heritability of this trait was high. Despite comparatively low intra-species variability, some cultivars were identified that may be promising candidates for breeding for naturally low ATI contents.</description><subject>631/449/1870</subject><subject>639/638/11/296</subject><subject>639/638/45/475</subject><subject>639/638/45/612</subject><subject>Action potential</subject><subject>Amylases - antagonists & inhibitors</subject><subject>Amylases - classification</subject><subject>Arrhythmia</subject><subject>Cardiac arrhythmia</subject><subject>Cardiomyocytes</subject><subject>Chromatography, Liquid - methods</subject><subject>Cultivars</subject><subject>Drug discovery</subject><subject>Germany</subject><subject>Glucocorticoids</subject><subject>Gluten</subject><subject>Heart</subject><subject>Heart diseases</subject><subject>Humanities and Social Sciences</subject><subject>Liquid chromatography</subject><subject>Long QT syndrome</subject><subject>Mass spectrometry</subject><subject>multidisciplinary</subject><subject>Phosphorylation</subject><subject>Plant Proteins - analysis</subject><subject>Pluripotency</subject><subject>Prostate cancer</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Sodium channels (voltage-gated)</subject><subject>Stable isotopes</subject><subject>Stem cells</subject><subject>Tandem Mass Spectrometry - methods</subject><subject>Triticum - growth & development</subject><subject>Triticum - metabolism</subject><subject>Trypsin - chemistry</subject><subject>Trypsin Inhibitors - analysis</subject><subject>Wheat</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kc9u3CAQxq2qURMleYEeKqReenGXAbyYS6Vqlf6RNsoh6RkBxgmRDQ7gSJtT36Fv2CcprdNoU6lcZtD85mOYr6peA34PmLarxKARbY0JrjkwoPXDi-qIYNbUhBLyci8_rE5TusXlNEQwEK-qQ0raloqWHFV5E8ZJRZXdvUV3s_LZ5eWy3fz8_uP8cnV-iZRXwy65hEKPgCI17gaV7CrH3ZScR87fOO1yiKmkBTbO-lxih8bQ2ejRVXTZmXlEabKlmE6qg14NyZ4-xuPq26ezq82Xenvx-evm47Y2DUCuKROE6L5TXGiuNHS9ZoR2WIHueqyM1Rx6zgCEAWg6qjm2XFHB6XrNRG_ocfVh0Z1mPdrOlLGiGuQU3ajiTgbl5POKdzfyOtxLzjhQYEXg3aNADHezTVmOLhk7DMrbMCdJGMNsXZZKCvr2H_Q2zLEsLkloBRVrShkvFFkoE0NK0fZPwwCWv32Vi6-y-Cr_-CofStOb_W88tfx1sQB0AVIp-Wsb997-v-wvzRCxhw</recordid><startdate>20200903</startdate><enddate>20200903</enddate><creator>Geisslitz, Sabrina</creator><creator>Longin, C. 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Friedrich H.</creatorcontrib><creatorcontrib>Koehler, Peter</creatorcontrib><creatorcontrib>Scherf, Katharina Anne</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Geisslitz, Sabrina</au><au>Longin, C. Friedrich H.</au><au>Koehler, Peter</au><au>Scherf, Katharina Anne</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative quantitative LC–MS/MS analysis of 13 amylase/trypsin inhibitors in ancient and modern Triticum species</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2020-09-03</date><risdate>2020</risdate><volume>10</volume><issue>1</issue><spage>14570</spage><epage>14570</epage><pages>14570-14570</pages><artnum>14570</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Amylase/trypsin inhibitors (ATIs) are major wheat allergens and they are also implicated in causing non-celiac gluten sensitivity and worsening other inflammatory conditions. With only few studies on ATI contents in different
Triticum
species available so far, we developed a targeted liquid chromatography-tandem mass spectrometry (LC–MS/MS) method based on stable isotope dilution assays to quantitate the 13 most important ATIs in a well-defined sample set of eight cultivars of common wheat and durum wheat (modern species), as well as spelt, emmer and einkorn (ancient species) grown at three locations in Germany, respectively. Only few ATIs with low contents were detected in einkorn. In contrast, spelt had the highest total ATI contents. Emmer and common wheat had similar total ATI contents, with durum wheat having lower contents than common wheat. Due to the lack of correlation, it was not possible to estimate ATI contents based on crude protein contents. The wheat species had a higher influence on ATI contents than the growing location and the heritability of this trait was high. Despite comparatively low intra-species variability, some cultivars were identified that may be promising candidates for breeding for naturally low ATI contents.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>32883982</pmid><doi>10.1038/s41598-020-71413-z</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/449/1870 639/638/11/296 639/638/45/475 639/638/45/612 Action potential Amylases - antagonists & inhibitors Amylases - classification Arrhythmia Cardiac arrhythmia Cardiomyocytes Chromatography, Liquid - methods Cultivars Drug discovery Germany Glucocorticoids Gluten Heart Heart diseases Humanities and Social Sciences Liquid chromatography Long QT syndrome Mass spectrometry multidisciplinary Phosphorylation Plant Proteins - analysis Pluripotency Prostate cancer Science Science (multidisciplinary) Sodium channels (voltage-gated) Stable isotopes Stem cells Tandem Mass Spectrometry - methods Triticum - growth & development Triticum - metabolism Trypsin - chemistry Trypsin Inhibitors - analysis Wheat |
title | Comparative quantitative LC–MS/MS analysis of 13 amylase/trypsin inhibitors in ancient and modern Triticum species |
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