Simple Turn-On Fluorescent Sensor for Discriminating Cys/Hcy and GSH from Different Fluorescent Signals
As a kind of bioactive sulfur species, biothiols (Cys, Hcy, and GSH) play an irreplaceable role in regulating the redox balance of life processes. Because of their similar chemical structures and properties, a sulfydryl group, and an amino group, it is an important challenge to distinguish two or mo...
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Veröffentlicht in: | Analytical chemistry (Washington) 2021-02, Vol.93 (4), p.2244-2253 |
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creator | Wang, Xiao-Bo Li, Hui-Jing Liu, Chang Hu, Yun-Xiang Li, Meng-Chen Wu, Yan-Chao |
description | As a kind of bioactive sulfur species, biothiols (Cys, Hcy, and GSH) play an irreplaceable role in regulating the redox balance of life processes. Because of their similar chemical structures and properties, a sulfydryl group, and an amino group, it is an important challenge to distinguish two or more of them at the same time. Herein, a fluorescent sensor (NTPC) based on the coumarin structure was developed to discriminate Cys/Hcy and GSH simultaneously. The sensor has no fluorescence due to the d-PET effect but displays strong fluorescence after its reaction with biothiols. There are two potential reaction sites (nitrophenyl sulfide group and aldehyde group) in the structure of NTPC, resulting in different fluorescent signal changes after reacting with biothiols (green for Cys and Hcy and red for GSH). Under double-wavelength excitation, the sensor shows low background fluorescence, high selectivity, and low detection limits toward biothiols. Moreover, the sensor can be used to discriminate different biothiols (Cys/Hcy and GSH) in cells and zebra fish by different fluorescence signals with low toxicity and might provide a promising tool for studying the roles of different biothiols in various physiological and pathological processes. |
doi_str_mv | 10.1021/acs.analchem.0c04100 |
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Because of their similar chemical structures and properties, a sulfydryl group, and an amino group, it is an important challenge to distinguish two or more of them at the same time. Herein, a fluorescent sensor (NTPC) based on the coumarin structure was developed to discriminate Cys/Hcy and GSH simultaneously. The sensor has no fluorescence due to the d-PET effect but displays strong fluorescence after its reaction with biothiols. There are two potential reaction sites (nitrophenyl sulfide group and aldehyde group) in the structure of NTPC, resulting in different fluorescent signal changes after reacting with biothiols (green for Cys and Hcy and red for GSH). Under double-wavelength excitation, the sensor shows low background fluorescence, high selectivity, and low detection limits toward biothiols. Moreover, the sensor can be used to discriminate different biothiols (Cys/Hcy and GSH) in cells and zebra fish by different fluorescence signals with low toxicity and might provide a promising tool for studying the roles of different biothiols in various physiological and pathological processes.</description><identifier>ISSN: 0003-2700</identifier><identifier>EISSN: 1520-6882</identifier><identifier>DOI: 10.1021/acs.analchem.0c04100</identifier><identifier>PMID: 33399443</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Aldehydes ; Animals ; Biocompatibility ; Chemistry ; Coumarin ; Cysteine ; Detection limits ; Fluorescence ; Fluorescence in situ hybridization ; Fluorescent Dyes ; Glutathione - chemistry ; Homocysteine - chemistry ; Molecular Structure ; Selectivity ; Sensors ; Sulfide ; Sulfur ; Toxicity ; Zebrafish</subject><ispartof>Analytical chemistry (Washington), 2021-02, Vol.93 (4), p.2244-2253</ispartof><rights>2021 American Chemical Society</rights><rights>Copyright American Chemical Society Feb 2, 2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a376t-d9cde02d098b117e9cd1532e287c664df85b068a800a1e62de68afb8690fdf8b3</citedby><cites>FETCH-LOGICAL-a376t-d9cde02d098b117e9cd1532e287c664df85b068a800a1e62de68afb8690fdf8b3</cites><orcidid>0000-0002-0111-7484</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.analchem.0c04100$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.analchem.0c04100$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33399443$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Xiao-Bo</creatorcontrib><creatorcontrib>Li, Hui-Jing</creatorcontrib><creatorcontrib>Liu, Chang</creatorcontrib><creatorcontrib>Hu, Yun-Xiang</creatorcontrib><creatorcontrib>Li, Meng-Chen</creatorcontrib><creatorcontrib>Wu, Yan-Chao</creatorcontrib><title>Simple Turn-On Fluorescent Sensor for Discriminating Cys/Hcy and GSH from Different Fluorescent Signals</title><title>Analytical chemistry (Washington)</title><addtitle>Anal. Chem</addtitle><description>As a kind of bioactive sulfur species, biothiols (Cys, Hcy, and GSH) play an irreplaceable role in regulating the redox balance of life processes. Because of their similar chemical structures and properties, a sulfydryl group, and an amino group, it is an important challenge to distinguish two or more of them at the same time. Herein, a fluorescent sensor (NTPC) based on the coumarin structure was developed to discriminate Cys/Hcy and GSH simultaneously. The sensor has no fluorescence due to the d-PET effect but displays strong fluorescence after its reaction with biothiols. There are two potential reaction sites (nitrophenyl sulfide group and aldehyde group) in the structure of NTPC, resulting in different fluorescent signal changes after reacting with biothiols (green for Cys and Hcy and red for GSH). Under double-wavelength excitation, the sensor shows low background fluorescence, high selectivity, and low detection limits toward biothiols. Moreover, the sensor can be used to discriminate different biothiols (Cys/Hcy and GSH) in cells and zebra fish by different fluorescence signals with low toxicity and might provide a promising tool for studying the roles of different biothiols in various physiological and pathological processes.</description><subject>Aldehydes</subject><subject>Animals</subject><subject>Biocompatibility</subject><subject>Chemistry</subject><subject>Coumarin</subject><subject>Cysteine</subject><subject>Detection limits</subject><subject>Fluorescence</subject><subject>Fluorescence in situ hybridization</subject><subject>Fluorescent Dyes</subject><subject>Glutathione - chemistry</subject><subject>Homocysteine - chemistry</subject><subject>Molecular Structure</subject><subject>Selectivity</subject><subject>Sensors</subject><subject>Sulfide</subject><subject>Sulfur</subject><subject>Toxicity</subject><subject>Zebrafish</subject><issn>0003-2700</issn><issn>1520-6882</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUFr4zAQhUVpadPu_oNlMfSyF6cjyZal45LdNIVCD2nPRpZHWRdbzkrxIf9-JyQtbA89iGHQ994M8xj7xmHOQfA769LcBtu7PzjMwUHBAc7YjJcCcqW1OGczAJC5qACu2HVKrwCcA1eX7EpKaUxRyBnbrLth22P2PMWQP4Vs2U9jxOQw7LI1hjTGzNP71SUXu6ELdteFTbbYp7uV22c2tNn9epX5OA7EeI_xIPzPpNvQkukLu_BU8Oup3rCX5e_nxSp_fLp_WPx8zK2s1C5vjWsRRAtGN5xXSC0vpUChK6dU0XpdNqC01QCWoxItUuMbrQx4-mzkDftx9N3G8e-EaVcPtDr2vQ04TqkWRVVKo0ulCL39gL6OdAXajigDQgljDFHFkXJxTCmir7d0CBv3NYf6EERNQdRvQdSnIEj2_WQ-NQO276K3yxMAR-Agfx_8qec_dMyXdA</recordid><startdate>20210202</startdate><enddate>20210202</enddate><creator>Wang, Xiao-Bo</creator><creator>Li, Hui-Jing</creator><creator>Liu, Chang</creator><creator>Hu, Yun-Xiang</creator><creator>Li, Meng-Chen</creator><creator>Wu, Yan-Chao</creator><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>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7TM</scope><scope>7U5</scope><scope>7U7</scope><scope>7U9</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0111-7484</orcidid></search><sort><creationdate>20210202</creationdate><title>Simple Turn-On Fluorescent Sensor for Discriminating Cys/Hcy and GSH from Different Fluorescent Signals</title><author>Wang, Xiao-Bo ; Li, Hui-Jing ; Liu, Chang ; Hu, Yun-Xiang ; Li, Meng-Chen ; Wu, Yan-Chao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a376t-d9cde02d098b117e9cd1532e287c664df85b068a800a1e62de68afb8690fdf8b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Aldehydes</topic><topic>Animals</topic><topic>Biocompatibility</topic><topic>Chemistry</topic><topic>Coumarin</topic><topic>Cysteine</topic><topic>Detection limits</topic><topic>Fluorescence</topic><topic>Fluorescence in situ hybridization</topic><topic>Fluorescent Dyes</topic><topic>Glutathione - chemistry</topic><topic>Homocysteine - chemistry</topic><topic>Molecular Structure</topic><topic>Selectivity</topic><topic>Sensors</topic><topic>Sulfide</topic><topic>Sulfur</topic><topic>Toxicity</topic><topic>Zebrafish</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Xiao-Bo</creatorcontrib><creatorcontrib>Li, Hui-Jing</creatorcontrib><creatorcontrib>Liu, Chang</creatorcontrib><creatorcontrib>Hu, Yun-Xiang</creatorcontrib><creatorcontrib>Li, Meng-Chen</creatorcontrib><creatorcontrib>Wu, Yan-Chao</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Analytical chemistry (Washington)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Xiao-Bo</au><au>Li, Hui-Jing</au><au>Liu, Chang</au><au>Hu, Yun-Xiang</au><au>Li, Meng-Chen</au><au>Wu, Yan-Chao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Simple Turn-On Fluorescent Sensor for Discriminating Cys/Hcy and GSH from Different Fluorescent Signals</atitle><jtitle>Analytical chemistry (Washington)</jtitle><addtitle>Anal. Chem</addtitle><date>2021-02-02</date><risdate>2021</risdate><volume>93</volume><issue>4</issue><spage>2244</spage><epage>2253</epage><pages>2244-2253</pages><issn>0003-2700</issn><eissn>1520-6882</eissn><abstract>As a kind of bioactive sulfur species, biothiols (Cys, Hcy, and GSH) play an irreplaceable role in regulating the redox balance of life processes. Because of their similar chemical structures and properties, a sulfydryl group, and an amino group, it is an important challenge to distinguish two or more of them at the same time. Herein, a fluorescent sensor (NTPC) based on the coumarin structure was developed to discriminate Cys/Hcy and GSH simultaneously. The sensor has no fluorescence due to the d-PET effect but displays strong fluorescence after its reaction with biothiols. There are two potential reaction sites (nitrophenyl sulfide group and aldehyde group) in the structure of NTPC, resulting in different fluorescent signal changes after reacting with biothiols (green for Cys and Hcy and red for GSH). Under double-wavelength excitation, the sensor shows low background fluorescence, high selectivity, and low detection limits toward biothiols. Moreover, the sensor can be used to discriminate different biothiols (Cys/Hcy and GSH) in cells and zebra fish by different fluorescence signals with low toxicity and might provide a promising tool for studying the roles of different biothiols in various physiological and pathological processes.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>33399443</pmid><doi>10.1021/acs.analchem.0c04100</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-0111-7484</orcidid></addata></record> |
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subjects | Aldehydes Animals Biocompatibility Chemistry Coumarin Cysteine Detection limits Fluorescence Fluorescence in situ hybridization Fluorescent Dyes Glutathione - chemistry Homocysteine - chemistry Molecular Structure Selectivity Sensors Sulfide Sulfur Toxicity Zebrafish |
title | Simple Turn-On Fluorescent Sensor for Discriminating Cys/Hcy and GSH from Different Fluorescent Signals |
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