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An immunosensor based on antibody binding fragments attached to gold nanoparticles for the detection of peptides derived from avian influenza hemagglutinin H5
This paper concerns the development of an immunosensor for detection of peptides derived from avian influenza hemagglutinin H5. Its preparation consists of successive gold electrode modification steps: (i) modification with 1,6-hexanedithiol and gold colloidal nanoparticles; (ii) immobilization of a...
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Published in: | Sensors (Basel, Switzerland) Switzerland), 2014-08, Vol.14 (9), p.15714-15728 |
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creator | Jarocka, Urszula Sawicka, Róża Góra-Sochacka, Anna Sirko, Agnieszka Zagórski-Ostoja, Włodzimierz Radecki, Jerzy Radecka, Hanna |
description | This paper concerns the development of an immunosensor for detection of peptides derived from avian influenza hemagglutinin H5. Its preparation consists of successive gold electrode modification steps: (i) modification with 1,6-hexanedithiol and gold colloidal nanoparticles; (ii) immobilization of antibody-binding fragments (Fab') of anti-hemagglutinin H5 monoclonal antibodies Mab 6-9-1 via S-Au covalent bonds; and (iii) covering the remaining free space on the electrode surfaces with bovine serum albumin. The interactions between Fab' fragments and hemagglutinin (HA) variants have been explored with electrochemical impedance spectroscopy (EIS) in the presence of [Fe(CN)6](3-/4-) as an electroactive marker. The immunosensor was able to recognize three different His-tagged variants of recombinant hemagglutinin from H5N1 viruses: H1 subunit (17-340 residues) of A/swan/Poland/305-135V08/2006, the long HA (17-530 residues) A/Bar-headed Goose/Qinghai/12/2005 and H1 subunit (1-345 residues) of A/Vietnam/1194/2004. The strongest response has been observed for the long variant with detection limit of 2.2 pg/mL and dynamic range from 4.0 to 20.0 pg/mL. |
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Its preparation consists of successive gold electrode modification steps: (i) modification with 1,6-hexanedithiol and gold colloidal nanoparticles; (ii) immobilization of antibody-binding fragments (Fab') of anti-hemagglutinin H5 monoclonal antibodies Mab 6-9-1 via S-Au covalent bonds; and (iii) covering the remaining free space on the electrode surfaces with bovine serum albumin. The interactions between Fab' fragments and hemagglutinin (HA) variants have been explored with electrochemical impedance spectroscopy (EIS) in the presence of [Fe(CN)6](3-/4-) as an electroactive marker. The immunosensor was able to recognize three different His-tagged variants of recombinant hemagglutinin from H5N1 viruses: H1 subunit (17-340 residues) of A/swan/Poland/305-135V08/2006, the long HA (17-530 residues) A/Bar-headed Goose/Qinghai/12/2005 and H1 subunit (1-345 residues) of A/Vietnam/1194/2004. The strongest response has been observed for the long variant with detection limit of 2.2 pg/mL and dynamic range from 4.0 to 20.0 pg/mL.</description><identifier>ISSN: 1424-8220</identifier><identifier>EISSN: 1424-8220</identifier><identifier>DOI: 10.3390/s140915714</identifier><identifier>PMID: 25157550</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Antibodies ; Antibodies, Viral - immunology ; Antigens ; Avian flu ; avian influenza virus ; Biosensing Techniques - instrumentation ; Biosensors ; Chemical bonds ; Dielectric Spectroscopy - instrumentation ; electrochemical immunosensor ; electrochemical impedance spectroscopy ; Electrodes ; Enzymes ; Equipment Design ; Equipment Failure Analysis ; Fab’ fragments ; Gold ; Gold - chemistry ; gold electrodes ; Hemagglutinin Glycoproteins, Influenza Virus - analysis ; Hemagglutinin Glycoproteins, Influenza Virus - immunology ; Immunoassay - instrumentation ; Immunoglobulin Fragments - immunology ; Influenza A Virus, H5N1 Subtype - immunology ; Metal Nanoparticles - chemistry ; Metal Nanoparticles - ultrastructure ; Nanoparticles ; Nanotechnology - instrumentation ; Peptides - immunology ; Polypeptides ; Potassium ; Poultry ; Sensors ; Viruses</subject><ispartof>Sensors (Basel, Switzerland), 2014-08, Vol.14 (9), p.15714-15728</ispartof><rights>Copyright MDPI AG 2014</rights><rights>2014 by the authors; licensee MDPI, Basel, Switzerland. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c608t-4bd0304cc60f0b52cf75b565d6cbcfe074562ee1e8bcc621241dc0b1f12849a33</citedby><cites>FETCH-LOGICAL-c608t-4bd0304cc60f0b52cf75b565d6cbcfe074562ee1e8bcc621241dc0b1f12849a33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1615943401/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1615943401?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25157550$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jarocka, Urszula</creatorcontrib><creatorcontrib>Sawicka, Róża</creatorcontrib><creatorcontrib>Góra-Sochacka, Anna</creatorcontrib><creatorcontrib>Sirko, Agnieszka</creatorcontrib><creatorcontrib>Zagórski-Ostoja, Włodzimierz</creatorcontrib><creatorcontrib>Radecki, Jerzy</creatorcontrib><creatorcontrib>Radecka, Hanna</creatorcontrib><title>An immunosensor based on antibody binding fragments attached to gold nanoparticles for the detection of peptides derived from avian influenza hemagglutinin H5</title><title>Sensors (Basel, Switzerland)</title><addtitle>Sensors (Basel)</addtitle><description>This paper concerns the development of an immunosensor for detection of peptides derived from avian influenza hemagglutinin H5. Its preparation consists of successive gold electrode modification steps: (i) modification with 1,6-hexanedithiol and gold colloidal nanoparticles; (ii) immobilization of antibody-binding fragments (Fab') of anti-hemagglutinin H5 monoclonal antibodies Mab 6-9-1 via S-Au covalent bonds; and (iii) covering the remaining free space on the electrode surfaces with bovine serum albumin. The interactions between Fab' fragments and hemagglutinin (HA) variants have been explored with electrochemical impedance spectroscopy (EIS) in the presence of [Fe(CN)6](3-/4-) as an electroactive marker. The immunosensor was able to recognize three different His-tagged variants of recombinant hemagglutinin from H5N1 viruses: H1 subunit (17-340 residues) of A/swan/Poland/305-135V08/2006, the long HA (17-530 residues) A/Bar-headed Goose/Qinghai/12/2005 and H1 subunit (1-345 residues) of A/Vietnam/1194/2004. The strongest response has been observed for the long variant with detection limit of 2.2 pg/mL and dynamic range from 4.0 to 20.0 pg/mL.</description><subject>Antibodies</subject><subject>Antibodies, Viral - immunology</subject><subject>Antigens</subject><subject>Avian flu</subject><subject>avian influenza virus</subject><subject>Biosensing Techniques - instrumentation</subject><subject>Biosensors</subject><subject>Chemical bonds</subject><subject>Dielectric Spectroscopy - instrumentation</subject><subject>electrochemical immunosensor</subject><subject>electrochemical impedance spectroscopy</subject><subject>Electrodes</subject><subject>Enzymes</subject><subject>Equipment Design</subject><subject>Equipment Failure Analysis</subject><subject>Fab’ fragments</subject><subject>Gold</subject><subject>Gold - chemistry</subject><subject>gold electrodes</subject><subject>Hemagglutinin Glycoproteins, Influenza Virus - analysis</subject><subject>Hemagglutinin Glycoproteins, Influenza Virus - immunology</subject><subject>Immunoassay - instrumentation</subject><subject>Immunoglobulin Fragments - immunology</subject><subject>Influenza A Virus, H5N1 Subtype - immunology</subject><subject>Metal Nanoparticles - chemistry</subject><subject>Metal Nanoparticles - ultrastructure</subject><subject>Nanoparticles</subject><subject>Nanotechnology - instrumentation</subject><subject>Peptides - immunology</subject><subject>Polypeptides</subject><subject>Potassium</subject><subject>Poultry</subject><subject>Sensors</subject><subject>Viruses</subject><issn>1424-8220</issn><issn>1424-8220</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpVksluFDEQQFsIRBa48AHIEjekAa-9XJCiCJJIkbjA2fJS7vGo225s90jJx_CtOMwQkpOXen5VZVXTvCP4E2MD_pwJxwMRHeEvmlPCKd_0lOKXT_YnzVnOO4wpY6x_3ZxQUXEh8Gnz-yIgP89riBlCjglplcGiGJAKxeto75D2wfowIpfUOEMoGalSlNlWrEQ0xsmioEJcVCreTJCRq5qyBWShgCm-uqJDCyzF2xq1kPy-vnUpzkjtvaoFBDetEO4V2sKsxnFaiw8-oGvxpnnl1JTh7XE9b35--_rj8npz-_3q5vLidmNa3JcN1xYzzE09OawFNa4TWrTCtkYbB7jjoqUABHpdGUooJ9ZgTRyhPR8UY-fNzcFro9rJJflZpTsZlZd_L2Ia5bE9yRxvB2I1Zv3AedcrigEPbUsds7QboLq-HFzLqmewpn5ZUtMz6fNI8Fs5xr3kFPeEkyr4cBSk-GuFXOQurinU_iVpiRg44_iB-nigTIo5J3CPGQiWD3Mh_89Fhd8_rekR_TcI7A-xa7YX</recordid><startdate>20140825</startdate><enddate>20140825</enddate><creator>Jarocka, Urszula</creator><creator>Sawicka, Róża</creator><creator>Góra-Sochacka, Anna</creator><creator>Sirko, Agnieszka</creator><creator>Zagórski-Ostoja, Włodzimierz</creator><creator>Radecki, Jerzy</creator><creator>Radecka, Hanna</creator><general>MDPI AG</general><general>MDPI</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>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20140825</creationdate><title>An immunosensor based on antibody binding fragments attached to gold nanoparticles for the detection of peptides derived from avian influenza hemagglutinin H5</title><author>Jarocka, Urszula ; Sawicka, Róża ; Góra-Sochacka, Anna ; Sirko, Agnieszka ; Zagórski-Ostoja, Włodzimierz ; Radecki, Jerzy ; Radecka, Hanna</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c608t-4bd0304cc60f0b52cf75b565d6cbcfe074562ee1e8bcc621241dc0b1f12849a33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Antibodies</topic><topic>Antibodies, Viral - immunology</topic><topic>Antigens</topic><topic>Avian flu</topic><topic>avian influenza virus</topic><topic>Biosensing Techniques - instrumentation</topic><topic>Biosensors</topic><topic>Chemical bonds</topic><topic>Dielectric Spectroscopy - instrumentation</topic><topic>electrochemical immunosensor</topic><topic>electrochemical impedance spectroscopy</topic><topic>Electrodes</topic><topic>Enzymes</topic><topic>Equipment Design</topic><topic>Equipment Failure Analysis</topic><topic>Fab’ fragments</topic><topic>Gold</topic><topic>Gold - chemistry</topic><topic>gold electrodes</topic><topic>Hemagglutinin Glycoproteins, Influenza Virus - analysis</topic><topic>Hemagglutinin Glycoproteins, Influenza Virus - immunology</topic><topic>Immunoassay - instrumentation</topic><topic>Immunoglobulin Fragments - immunology</topic><topic>Influenza A Virus, H5N1 Subtype - immunology</topic><topic>Metal Nanoparticles - chemistry</topic><topic>Metal Nanoparticles - ultrastructure</topic><topic>Nanoparticles</topic><topic>Nanotechnology - instrumentation</topic><topic>Peptides - immunology</topic><topic>Polypeptides</topic><topic>Potassium</topic><topic>Poultry</topic><topic>Sensors</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jarocka, Urszula</creatorcontrib><creatorcontrib>Sawicka, Róża</creatorcontrib><creatorcontrib>Góra-Sochacka, Anna</creatorcontrib><creatorcontrib>Sirko, Agnieszka</creatorcontrib><creatorcontrib>Zagórski-Ostoja, Włodzimierz</creatorcontrib><creatorcontrib>Radecki, Jerzy</creatorcontrib><creatorcontrib>Radecka, Hanna</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>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</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 Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content (ProQuest)</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>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Sensors (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jarocka, Urszula</au><au>Sawicka, Róża</au><au>Góra-Sochacka, Anna</au><au>Sirko, Agnieszka</au><au>Zagórski-Ostoja, Włodzimierz</au><au>Radecki, Jerzy</au><au>Radecka, Hanna</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An immunosensor based on antibody binding fragments attached to gold nanoparticles for the detection of peptides derived from avian influenza hemagglutinin H5</atitle><jtitle>Sensors (Basel, Switzerland)</jtitle><addtitle>Sensors (Basel)</addtitle><date>2014-08-25</date><risdate>2014</risdate><volume>14</volume><issue>9</issue><spage>15714</spage><epage>15728</epage><pages>15714-15728</pages><issn>1424-8220</issn><eissn>1424-8220</eissn><abstract>This paper concerns the development of an immunosensor for detection of peptides derived from avian influenza hemagglutinin H5. Its preparation consists of successive gold electrode modification steps: (i) modification with 1,6-hexanedithiol and gold colloidal nanoparticles; (ii) immobilization of antibody-binding fragments (Fab') of anti-hemagglutinin H5 monoclonal antibodies Mab 6-9-1 via S-Au covalent bonds; and (iii) covering the remaining free space on the electrode surfaces with bovine serum albumin. The interactions between Fab' fragments and hemagglutinin (HA) variants have been explored with electrochemical impedance spectroscopy (EIS) in the presence of [Fe(CN)6](3-/4-) as an electroactive marker. The immunosensor was able to recognize three different His-tagged variants of recombinant hemagglutinin from H5N1 viruses: H1 subunit (17-340 residues) of A/swan/Poland/305-135V08/2006, the long HA (17-530 residues) A/Bar-headed Goose/Qinghai/12/2005 and H1 subunit (1-345 residues) of A/Vietnam/1194/2004. The strongest response has been observed for the long variant with detection limit of 2.2 pg/mL and dynamic range from 4.0 to 20.0 pg/mL.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>25157550</pmid><doi>10.3390/s140915714</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antibodies Antibodies, Viral - immunology Antigens Avian flu avian influenza virus Biosensing Techniques - instrumentation Biosensors Chemical bonds Dielectric Spectroscopy - instrumentation electrochemical immunosensor electrochemical impedance spectroscopy Electrodes Enzymes Equipment Design Equipment Failure Analysis Fab’ fragments Gold Gold - chemistry gold electrodes Hemagglutinin Glycoproteins, Influenza Virus - analysis Hemagglutinin Glycoproteins, Influenza Virus - immunology Immunoassay - instrumentation Immunoglobulin Fragments - immunology Influenza A Virus, H5N1 Subtype - immunology Metal Nanoparticles - chemistry Metal Nanoparticles - ultrastructure Nanoparticles Nanotechnology - instrumentation Peptides - immunology Polypeptides Potassium Poultry Sensors Viruses |
title | An immunosensor based on antibody binding fragments attached to gold nanoparticles for the detection of peptides derived from avian influenza hemagglutinin H5 |
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