Immunochromatographic assay of T-2 toxin using labeled anti-species antibodies

A new scheme of immunochromatographic assay was developed for the highly sensitive detection of low-molecular-weight analytes. This scheme includes the following two steps: the formation of complexes of free specific antibodies with an antigen and their detection by anti-species antibodies conjugate...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Applied biochemistry and microbiology 2017-09, Vol.53 (5), p.594-599
Hauptverfasser: Urusov, A. E., Petrakova, A. V., Bartosh, A. V., Gubaydullina, M. K., Zherdev, A. V., Dzantiev, B. B.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 599
container_issue 5
container_start_page 594
container_title Applied biochemistry and microbiology
container_volume 53
creator Urusov, A. E.
Petrakova, A. V.
Bartosh, A. V.
Gubaydullina, M. K.
Zherdev, A. V.
Dzantiev, B. B.
description A new scheme of immunochromatographic assay was developed for the highly sensitive detection of low-molecular-weight analytes. This scheme includes the following two steps: the formation of complexes of free specific antibodies with an antigen and their detection by anti-species antibodies conjugated to gold nanoparticles as the label. This scheme was tested with mycotoxin T-2 toxin in maize extracts. The use of specific antibodies and a label as two individual components made it possible to independently vary their concentrations with a simultaneous decrease in the detection limit and an increase in the color intensity. The assay did not require additional reagents and manipulations. The instrumental and visual detection limits of the designed test system were 0.1 and 5.0 ng/mL, respectively (2 and 90 ng per gram of analytes), which are two orders of magnitude lower compared to conventional immunochromatography using the same reagents.
doi_str_mv 10.1134/S0003683817050167
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1938393606</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1938393606</sourcerecordid><originalsourceid>FETCH-LOGICAL-c316t-a69afb9bd21524e2e6517e10264f75ff937420364db5a1fb577f0de5938219333</originalsourceid><addsrcrecordid>eNp1UE1LxDAQDaLguvoDvAU8RzNJkzRHWfxYWPTgei5pm-x22TY1acH996auB0E8zTzexzAPoWugtwA8u3ujlHKZ8xwUFRSkOkEzkDQnnLLsFM0mmkz8ObqIcZeglrmeoZdl246dr7bBt2bwm2D6bVNhE6M5YO_wmjA8-M-mw2Nsug3em9LubY1NNzQk9rZqbPwGpa_TeonOnNlHe_Uz5-j98WG9eCar16fl4n5FKg5yIEZq40pd1gwEyyyzUoCyQJnMnBLOaa4ylv7J6lIYcKVQytHaCs1zBppzPkc3x9w--I_RxqHY-TF06WSR-JxrLqlMKjiqquBjDNYVfWhaEw4F0GKqrfhTW_Kwoycmbbex4Vfyv6YvWgltuA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1938393606</pqid></control><display><type>article</type><title>Immunochromatographic assay of T-2 toxin using labeled anti-species antibodies</title><source>SpringerNature Journals</source><creator>Urusov, A. E. ; Petrakova, A. V. ; Bartosh, A. V. ; Gubaydullina, M. K. ; Zherdev, A. V. ; Dzantiev, B. B.</creator><creatorcontrib>Urusov, A. E. ; Petrakova, A. V. ; Bartosh, A. V. ; Gubaydullina, M. K. ; Zherdev, A. V. ; Dzantiev, B. B.</creatorcontrib><description>A new scheme of immunochromatographic assay was developed for the highly sensitive detection of low-molecular-weight analytes. This scheme includes the following two steps: the formation of complexes of free specific antibodies with an antigen and their detection by anti-species antibodies conjugated to gold nanoparticles as the label. This scheme was tested with mycotoxin T-2 toxin in maize extracts. The use of specific antibodies and a label as two individual components made it possible to independently vary their concentrations with a simultaneous decrease in the detection limit and an increase in the color intensity. The assay did not require additional reagents and manipulations. The instrumental and visual detection limits of the designed test system were 0.1 and 5.0 ng/mL, respectively (2 and 90 ng per gram of analytes), which are two orders of magnitude lower compared to conventional immunochromatography using the same reagents.</description><identifier>ISSN: 0003-6838</identifier><identifier>EISSN: 1608-3024</identifier><identifier>DOI: 10.1134/S0003683817050167</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Antibodies ; Assaying ; Biochemistry ; Biomedical and Life Sciences ; Detection limits ; Gold ; Immunoglobulins ; Life Sciences ; Medical Microbiology ; Microbiology ; Mycotoxins ; Nanoparticles ; Reagents ; Toxins</subject><ispartof>Applied biochemistry and microbiology, 2017-09, Vol.53 (5), p.594-599</ispartof><rights>Pleiades Publishing, Inc. 2017</rights><rights>Applied Biochemistry and Microbiology is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-a69afb9bd21524e2e6517e10264f75ff937420364db5a1fb577f0de5938219333</citedby><cites>FETCH-LOGICAL-c316t-a69afb9bd21524e2e6517e10264f75ff937420364db5a1fb577f0de5938219333</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S0003683817050167$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S0003683817050167$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Urusov, A. E.</creatorcontrib><creatorcontrib>Petrakova, A. V.</creatorcontrib><creatorcontrib>Bartosh, A. V.</creatorcontrib><creatorcontrib>Gubaydullina, M. K.</creatorcontrib><creatorcontrib>Zherdev, A. V.</creatorcontrib><creatorcontrib>Dzantiev, B. B.</creatorcontrib><title>Immunochromatographic assay of T-2 toxin using labeled anti-species antibodies</title><title>Applied biochemistry and microbiology</title><addtitle>Appl Biochem Microbiol</addtitle><description>A new scheme of immunochromatographic assay was developed for the highly sensitive detection of low-molecular-weight analytes. This scheme includes the following two steps: the formation of complexes of free specific antibodies with an antigen and their detection by anti-species antibodies conjugated to gold nanoparticles as the label. This scheme was tested with mycotoxin T-2 toxin in maize extracts. The use of specific antibodies and a label as two individual components made it possible to independently vary their concentrations with a simultaneous decrease in the detection limit and an increase in the color intensity. The assay did not require additional reagents and manipulations. The instrumental and visual detection limits of the designed test system were 0.1 and 5.0 ng/mL, respectively (2 and 90 ng per gram of analytes), which are two orders of magnitude lower compared to conventional immunochromatography using the same reagents.</description><subject>Antibodies</subject><subject>Assaying</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Detection limits</subject><subject>Gold</subject><subject>Immunoglobulins</subject><subject>Life Sciences</subject><subject>Medical Microbiology</subject><subject>Microbiology</subject><subject>Mycotoxins</subject><subject>Nanoparticles</subject><subject>Reagents</subject><subject>Toxins</subject><issn>0003-6838</issn><issn>1608-3024</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1UE1LxDAQDaLguvoDvAU8RzNJkzRHWfxYWPTgei5pm-x22TY1acH996auB0E8zTzexzAPoWugtwA8u3ujlHKZ8xwUFRSkOkEzkDQnnLLsFM0mmkz8ObqIcZeglrmeoZdl246dr7bBt2bwm2D6bVNhE6M5YO_wmjA8-M-mw2Nsug3em9LubY1NNzQk9rZqbPwGpa_TeonOnNlHe_Uz5-j98WG9eCar16fl4n5FKg5yIEZq40pd1gwEyyyzUoCyQJnMnBLOaa4ylv7J6lIYcKVQytHaCs1zBppzPkc3x9w--I_RxqHY-TF06WSR-JxrLqlMKjiqquBjDNYVfWhaEw4F0GKqrfhTW_Kwoycmbbex4Vfyv6YvWgltuA</recordid><startdate>20170901</startdate><enddate>20170901</enddate><creator>Urusov, A. E.</creator><creator>Petrakova, A. V.</creator><creator>Bartosh, A. V.</creator><creator>Gubaydullina, M. K.</creator><creator>Zherdev, A. V.</creator><creator>Dzantiev, B. B.</creator><general>Pleiades Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>20170901</creationdate><title>Immunochromatographic assay of T-2 toxin using labeled anti-species antibodies</title><author>Urusov, A. E. ; Petrakova, A. V. ; Bartosh, A. V. ; Gubaydullina, M. K. ; Zherdev, A. V. ; Dzantiev, B. B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-a69afb9bd21524e2e6517e10264f75ff937420364db5a1fb577f0de5938219333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Antibodies</topic><topic>Assaying</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Detection limits</topic><topic>Gold</topic><topic>Immunoglobulins</topic><topic>Life Sciences</topic><topic>Medical Microbiology</topic><topic>Microbiology</topic><topic>Mycotoxins</topic><topic>Nanoparticles</topic><topic>Reagents</topic><topic>Toxins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Urusov, A. E.</creatorcontrib><creatorcontrib>Petrakova, A. V.</creatorcontrib><creatorcontrib>Bartosh, A. V.</creatorcontrib><creatorcontrib>Gubaydullina, M. K.</creatorcontrib><creatorcontrib>Zherdev, A. V.</creatorcontrib><creatorcontrib>Dzantiev, B. B.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</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>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</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 &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</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><jtitle>Applied biochemistry and microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Urusov, A. E.</au><au>Petrakova, A. V.</au><au>Bartosh, A. V.</au><au>Gubaydullina, M. K.</au><au>Zherdev, A. V.</au><au>Dzantiev, B. B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunochromatographic assay of T-2 toxin using labeled anti-species antibodies</atitle><jtitle>Applied biochemistry and microbiology</jtitle><stitle>Appl Biochem Microbiol</stitle><date>2017-09-01</date><risdate>2017</risdate><volume>53</volume><issue>5</issue><spage>594</spage><epage>599</epage><pages>594-599</pages><issn>0003-6838</issn><eissn>1608-3024</eissn><abstract>A new scheme of immunochromatographic assay was developed for the highly sensitive detection of low-molecular-weight analytes. This scheme includes the following two steps: the formation of complexes of free specific antibodies with an antigen and their detection by anti-species antibodies conjugated to gold nanoparticles as the label. This scheme was tested with mycotoxin T-2 toxin in maize extracts. The use of specific antibodies and a label as two individual components made it possible to independently vary their concentrations with a simultaneous decrease in the detection limit and an increase in the color intensity. The assay did not require additional reagents and manipulations. The instrumental and visual detection limits of the designed test system were 0.1 and 5.0 ng/mL, respectively (2 and 90 ng per gram of analytes), which are two orders of magnitude lower compared to conventional immunochromatography using the same reagents.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S0003683817050167</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0003-6838
ispartof Applied biochemistry and microbiology, 2017-09, Vol.53 (5), p.594-599
issn 0003-6838
1608-3024
language eng
recordid cdi_proquest_journals_1938393606
source SpringerNature Journals
subjects Antibodies
Assaying
Biochemistry
Biomedical and Life Sciences
Detection limits
Gold
Immunoglobulins
Life Sciences
Medical Microbiology
Microbiology
Mycotoxins
Nanoparticles
Reagents
Toxins
title Immunochromatographic assay of T-2 toxin using labeled anti-species antibodies
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T07%3A15%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Immunochromatographic%20assay%20of%20T-2%20toxin%20using%20labeled%20anti-species%20antibodies&rft.jtitle=Applied%20biochemistry%20and%20microbiology&rft.au=Urusov,%20A.%20E.&rft.date=2017-09-01&rft.volume=53&rft.issue=5&rft.spage=594&rft.epage=599&rft.pages=594-599&rft.issn=0003-6838&rft.eissn=1608-3024&rft_id=info:doi/10.1134/S0003683817050167&rft_dat=%3Cproquest_cross%3E1938393606%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1938393606&rft_id=info:pmid/&rfr_iscdi=true