Enzyme-Coupled Nanoparticles-Assisted Laser Desorption Ionization Mass Spectrometry for Searching for Low-Mass Inhibitors of Enzymes in Complex Mixtures
In this report, enzyme-coupled magnetic nanoparticles (EMPs) were shown to be an effective affinity-based tool for finding specific interactions between enzymatic targets and the low-mass molecules in complex mixtures using classic MALDI-TOF apparatus. EMPs used in this work act as nonorganic matrix...
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Veröffentlicht in: | Journal of the American Society for Mass Spectrometry 2014-04, Vol.25 (4), p.538-547 |
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description | In this report, enzyme-coupled magnetic nanoparticles (EMPs) were shown to be an effective affinity-based tool for finding specific interactions between enzymatic targets and the low-mass molecules in complex mixtures using classic MALDI-TOF apparatus. EMPs used in this work act as nonorganic matrix enabling ionization of small molecules without any interference in the low-mass range (enzyme-coupled nanoparticles-assisted laser desorption ionization MS, ENALDI MS) and simultaneously carry the superficial specific binding sites to capture inhibitors present in a studied mixture. We evaluated ENALDI approach in two complementary variations: ‘ion fading’ (IF-ENALDI), based on superficial adsorption of inhibitors and ‘ion hunting’ (IH-ENALDI), based on selective pre-concentration of inhibitors. IF-ENALDI was applied for two sets of enzyme–inhibitor pairs: tyrosinase–glabridin and trypsin–leupeptin and for the real plant sample:
Sparrmannia discolor
leaf and stem methanol extract. The efficacy of IH-ENALDI was shown for the pair of trypsin–leupeptin. Both ENALDI approaches pose an alternative for bioassay-guided fractionation, the common method for finding inhibitors in the complex mixtures.
Figure
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doi_str_mv | 10.1007/s13361-014-0826-y |
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Sparrmannia discolor
leaf and stem methanol extract. The efficacy of IH-ENALDI was shown for the pair of trypsin–leupeptin. Both ENALDI approaches pose an alternative for bioassay-guided fractionation, the common method for finding inhibitors in the complex mixtures.
Figure
ᅟ</description><identifier>ISSN: 1044-0305</identifier><identifier>EISSN: 1879-1123</identifier><identifier>DOI: 10.1007/s13361-014-0826-y</identifier><identifier>PMID: 24549893</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Analytical Chemistry ; Binding sites ; Bioinformatics ; Biotechnology ; Chemical Sciences ; Chemistry ; Chemistry and Materials Science ; Coupling (molecular) ; Desorption ; Discoloration ; Enzyme Inhibitors - analysis ; Enzyme Inhibitors - isolation & purification ; Enzyme Inhibitors - metabolism ; Enzymes ; Enzymes, Immobilized - chemistry ; Enzymes, Immobilized - metabolism ; Fractionation ; Hunting ; Inhibitors ; Ionization ; Mass spectrometry ; Nanoparticles ; Nanoparticles - chemistry ; Organic Chemistry ; Plant Extracts - chemistry ; Proteomics ; Research Article ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods ; Trypsin ; Tyrosinase</subject><ispartof>Journal of the American Society for Mass Spectrometry, 2014-04, Vol.25 (4), p.538-547</ispartof><rights>American Society for Mass Spectrometry 2014</rights><rights>Journal of The American Society for Mass Spectrometry is a copyright of Springer, 2014.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c406t-be0f7039a01f9eab91ad6ae8fd9bc0e74f31cd5665d4e64e8f255681c6e491f83</citedby><cites>FETCH-LOGICAL-c406t-be0f7039a01f9eab91ad6ae8fd9bc0e74f31cd5665d4e64e8f255681c6e491f83</cites><orcidid>0000-0002-9894-1268 ; 0000-0002-8760-6018</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s13361-014-0826-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s13361-014-0826-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,776,780,881,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24549893$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-03465971$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Salwiński, Aleksander</creatorcontrib><creatorcontrib>Da Silva, David</creatorcontrib><creatorcontrib>Delépée, Raphaël</creatorcontrib><creatorcontrib>Maunit, Benoît</creatorcontrib><title>Enzyme-Coupled Nanoparticles-Assisted Laser Desorption Ionization Mass Spectrometry for Searching for Low-Mass Inhibitors of Enzymes in Complex Mixtures</title><title>Journal of the American Society for Mass Spectrometry</title><addtitle>J. Am. Soc. Mass Spectrom</addtitle><addtitle>J Am Soc Mass Spectrom</addtitle><description>In this report, enzyme-coupled magnetic nanoparticles (EMPs) were shown to be an effective affinity-based tool for finding specific interactions between enzymatic targets and the low-mass molecules in complex mixtures using classic MALDI-TOF apparatus. EMPs used in this work act as nonorganic matrix enabling ionization of small molecules without any interference in the low-mass range (enzyme-coupled nanoparticles-assisted laser desorption ionization MS, ENALDI MS) and simultaneously carry the superficial specific binding sites to capture inhibitors present in a studied mixture. We evaluated ENALDI approach in two complementary variations: ‘ion fading’ (IF-ENALDI), based on superficial adsorption of inhibitors and ‘ion hunting’ (IH-ENALDI), based on selective pre-concentration of inhibitors. IF-ENALDI was applied for two sets of enzyme–inhibitor pairs: tyrosinase–glabridin and trypsin–leupeptin and for the real plant sample:
Sparrmannia discolor
leaf and stem methanol extract. The efficacy of IH-ENALDI was shown for the pair of trypsin–leupeptin. Both ENALDI approaches pose an alternative for bioassay-guided fractionation, the common method for finding inhibitors in the complex mixtures.
Figure
ᅟ</description><subject>Analytical Chemistry</subject><subject>Binding sites</subject><subject>Bioinformatics</subject><subject>Biotechnology</subject><subject>Chemical Sciences</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Coupling (molecular)</subject><subject>Desorption</subject><subject>Discoloration</subject><subject>Enzyme Inhibitors - analysis</subject><subject>Enzyme Inhibitors - isolation & purification</subject><subject>Enzyme Inhibitors - metabolism</subject><subject>Enzymes</subject><subject>Enzymes, Immobilized - chemistry</subject><subject>Enzymes, Immobilized - metabolism</subject><subject>Fractionation</subject><subject>Hunting</subject><subject>Inhibitors</subject><subject>Ionization</subject><subject>Mass spectrometry</subject><subject>Nanoparticles</subject><subject>Nanoparticles - chemistry</subject><subject>Organic Chemistry</subject><subject>Plant Extracts - chemistry</subject><subject>Proteomics</subject><subject>Research Article</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods</subject><subject>Trypsin</subject><subject>Tyrosinase</subject><issn>1044-0305</issn><issn>1879-1123</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><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>eNp1kcFu1DAQhiMEoqXwAFyQJU4cTD2J48TH1VLoSikcCmfLSSZdV7tx8CTQ9El4XLybtuLCyeP5v_lnpD9J3oL4CEIU5wRZpoALkFyUqeLzs-QUykJzgDR7Hmsho5KJ_CR5RXQrBBRCFy-Tk1TmUpc6O03-XPT38x752k_DDlv21fZ-sGF0zQ6Jr4gcjbFdWcLAPiH5MIzO92zje3dvj-WVJWLXAzZj8Hscw8w6H9g12tBsXX9z_FX-Nz9ym37rajf6QMx3bFlOzPVs7ffxgDt25e7GKSC9Tl50dkf45uE9S358vvi-vuTVty-b9arijRRq5DWKrhCZtgI6jbbWYFtlsexaXTcCC9ll0LS5UnkrUckopHmuSmgUSg1dmZ0lHxbfrd2ZIbi9DbPx1pnLVWUOPZFJlesCfkFk3y_sEPzPCWk0t34KfTzPgM5FWYIEFSlYqCZ4ooDdky0Ic8jNLLmZmJs55GbmOPPuwXmq99g-TTwGFYF0AShK_Q2Gf1b_1_UvNPmmSw</recordid><startdate>20140401</startdate><enddate>20140401</enddate><creator>Salwiński, Aleksander</creator><creator>Da Silva, David</creator><creator>Delépée, Raphaël</creator><creator>Maunit, Benoît</creator><general>Springer US</general><general>Springer Nature B.V</general><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><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>1XC</scope><orcidid>https://orcid.org/0000-0002-9894-1268</orcidid><orcidid>https://orcid.org/0000-0002-8760-6018</orcidid></search><sort><creationdate>20140401</creationdate><title>Enzyme-Coupled Nanoparticles-Assisted Laser Desorption Ionization Mass Spectrometry for Searching for Low-Mass Inhibitors of Enzymes in Complex Mixtures</title><author>Salwiński, Aleksander ; Da Silva, David ; Delépée, Raphaël ; Maunit, Benoît</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c406t-be0f7039a01f9eab91ad6ae8fd9bc0e74f31cd5665d4e64e8f255681c6e491f83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Analytical Chemistry</topic><topic>Binding sites</topic><topic>Bioinformatics</topic><topic>Biotechnology</topic><topic>Chemical Sciences</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Coupling (molecular)</topic><topic>Desorption</topic><topic>Discoloration</topic><topic>Enzyme Inhibitors - analysis</topic><topic>Enzyme Inhibitors - isolation & purification</topic><topic>Enzyme Inhibitors - metabolism</topic><topic>Enzymes</topic><topic>Enzymes, Immobilized - chemistry</topic><topic>Enzymes, Immobilized - metabolism</topic><topic>Fractionation</topic><topic>Hunting</topic><topic>Inhibitors</topic><topic>Ionization</topic><topic>Mass spectrometry</topic><topic>Nanoparticles</topic><topic>Nanoparticles - chemistry</topic><topic>Organic Chemistry</topic><topic>Plant Extracts - chemistry</topic><topic>Proteomics</topic><topic>Research Article</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods</topic><topic>Trypsin</topic><topic>Tyrosinase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Salwiński, Aleksander</creatorcontrib><creatorcontrib>Da Silva, David</creatorcontrib><creatorcontrib>Delépée, Raphaël</creatorcontrib><creatorcontrib>Maunit, Benoît</creatorcontrib><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>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology 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>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</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 China</collection><collection>ProQuest Central Basic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Journal of the American Society for Mass Spectrometry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Salwiński, Aleksander</au><au>Da Silva, David</au><au>Delépée, Raphaël</au><au>Maunit, Benoît</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enzyme-Coupled Nanoparticles-Assisted Laser Desorption Ionization Mass Spectrometry for Searching for Low-Mass Inhibitors of Enzymes in Complex Mixtures</atitle><jtitle>Journal of the American Society for Mass Spectrometry</jtitle><stitle>J. Am. Soc. Mass Spectrom</stitle><addtitle>J Am Soc Mass Spectrom</addtitle><date>2014-04-01</date><risdate>2014</risdate><volume>25</volume><issue>4</issue><spage>538</spage><epage>547</epage><pages>538-547</pages><issn>1044-0305</issn><eissn>1879-1123</eissn><abstract>In this report, enzyme-coupled magnetic nanoparticles (EMPs) were shown to be an effective affinity-based tool for finding specific interactions between enzymatic targets and the low-mass molecules in complex mixtures using classic MALDI-TOF apparatus. EMPs used in this work act as nonorganic matrix enabling ionization of small molecules without any interference in the low-mass range (enzyme-coupled nanoparticles-assisted laser desorption ionization MS, ENALDI MS) and simultaneously carry the superficial specific binding sites to capture inhibitors present in a studied mixture. We evaluated ENALDI approach in two complementary variations: ‘ion fading’ (IF-ENALDI), based on superficial adsorption of inhibitors and ‘ion hunting’ (IH-ENALDI), based on selective pre-concentration of inhibitors. IF-ENALDI was applied for two sets of enzyme–inhibitor pairs: tyrosinase–glabridin and trypsin–leupeptin and for the real plant sample:
Sparrmannia discolor
leaf and stem methanol extract. The efficacy of IH-ENALDI was shown for the pair of trypsin–leupeptin. Both ENALDI approaches pose an alternative for bioassay-guided fractionation, the common method for finding inhibitors in the complex mixtures.
Figure
ᅟ</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>24549893</pmid><doi>10.1007/s13361-014-0826-y</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-9894-1268</orcidid><orcidid>https://orcid.org/0000-0002-8760-6018</orcidid></addata></record> |
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subjects | Analytical Chemistry Binding sites Bioinformatics Biotechnology Chemical Sciences Chemistry Chemistry and Materials Science Coupling (molecular) Desorption Discoloration Enzyme Inhibitors - analysis Enzyme Inhibitors - isolation & purification Enzyme Inhibitors - metabolism Enzymes Enzymes, Immobilized - chemistry Enzymes, Immobilized - metabolism Fractionation Hunting Inhibitors Ionization Mass spectrometry Nanoparticles Nanoparticles - chemistry Organic Chemistry Plant Extracts - chemistry Proteomics Research Article Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods Trypsin Tyrosinase |
title | Enzyme-Coupled Nanoparticles-Assisted Laser Desorption Ionization Mass Spectrometry for Searching for Low-Mass Inhibitors of Enzymes in Complex Mixtures |
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