Effective monitoring of protein reaction on glass plate surfaces by TOF-SIMS
Time-of-flight secondary ion mass spectrometry (TOF-SIMS) is capable of chemically visualizing proteins on insulated samples. Distribution of an immobilized probe protein, fluorescent-labeled protein A-immobilized on a glass plate, and that of a sample protein, immunogloblin G (IgG) in solution, rea...
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description | Time-of-flight secondary ion mass spectrometry (TOF-SIMS) is capable of chemically visualizing proteins on insulated samples. Distribution of an immobilized probe protein, fluorescent-labeled protein A-immobilized on a glass plate, and that of a sample protein, immunogloblin G (IgG) in solution, reacting with protein A on the biosensor surface, were evaluated with TOF-SIMS (TFS-2100, Physical Electronics). TOF-SIMS spectra and images of the protein on the glass plates were obtained, and this “mutual information”, as defined by information theory, was employed to analyze the TOF-SIMS spectra of proteins. Fragment ions from protein A and IgG were distinguished by the mutual, reinforcing information and specific fragment ions to each protein were selected to obtain the TOF-SIMS image of the protein. It is evident from the TOF-SIMS images of each protein that protein A was immobilized on the substrate homogeneously and that the reaction between the immobilized protein A and IgG is not localized in this condition. Chemical images of the proteins by TOF-SIMS will contribute to a better understanding of the reaction on the biosensor surface, and thus will help the development of more sophisticated biosensors. In addition, the requisite chemical conditions as well as the interaction between the biosensor surface and the immobilized proteins were investigated by TOF-SIMS by means of sets of reinforcing, mutually supportive information. |
doi_str_mv | 10.1016/j.bios.2004.06.040 |
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Distribution of an immobilized probe protein, fluorescent-labeled protein A-immobilized on a glass plate, and that of a sample protein, immunogloblin G (IgG) in solution, reacting with protein A on the biosensor surface, were evaluated with TOF-SIMS (TFS-2100, Physical Electronics). TOF-SIMS spectra and images of the protein on the glass plates were obtained, and this “mutual information”, as defined by information theory, was employed to analyze the TOF-SIMS spectra of proteins. Fragment ions from protein A and IgG were distinguished by the mutual, reinforcing information and specific fragment ions to each protein were selected to obtain the TOF-SIMS image of the protein. It is evident from the TOF-SIMS images of each protein that protein A was immobilized on the substrate homogeneously and that the reaction between the immobilized protein A and IgG is not localized in this condition. Chemical images of the proteins by TOF-SIMS will contribute to a better understanding of the reaction on the biosensor surface, and thus will help the development of more sophisticated biosensors. In addition, the requisite chemical conditions as well as the interaction between the biosensor surface and the immobilized proteins were investigated by TOF-SIMS by means of sets of reinforcing, mutually supportive information.</description><identifier>ISSN: 0956-5663</identifier><identifier>EISSN: 1873-4235</identifier><identifier>DOI: 10.1016/j.bios.2004.06.040</identifier><identifier>PMID: 15626618</identifier><language>eng</language><publisher>Lausanne: Elsevier B.V</publisher><subject>Adsorption ; Antigen-Antibody Complex - analysis ; Antigen-Antibody Complex - chemistry ; Antigen-Antibody Complex - immunology ; Antigen-Antibody Reactions - immunology ; Biological and medical sciences ; Biosensing Techniques - instrumentation ; Biosensing Techniques - methods ; Biosensors ; Biotechnology ; Chemical imaging ; Fundamental and applied biological sciences. Psychology ; Glass - chemistry ; Immunoassay - instrumentation ; Immunoassay - methods ; Immunoglobulin G - analysis ; Immunoglobulin G - chemistry ; Immunoglobulin G - immunology ; Information entropy ; Mass Spectrometry - instrumentation ; Mass Spectrometry - methods ; Methods. Procedures. Technologies ; Protein ; Protein Binding ; Protein Interaction Mapping - instrumentation ; Protein Interaction Mapping - methods ; Reproducibility of Results ; Sensitivity and Specificity ; Staphylococcal Protein A - analysis ; Staphylococcal Protein A - chemistry ; Staphylococcal Protein A - immunology ; TOF-SIMS ; Various methods and equipments</subject><ispartof>Biosensors & bioelectronics, 2005-02, Vol.20 (8), p.1626-1630</ispartof><rights>2004 Elsevier B.V.</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c481t-948ff6a2d9ad74cd65292a4b384ba615214f684a5d5f22fbf83d5cceaa86f3ac3</citedby><cites>FETCH-LOGICAL-c481t-948ff6a2d9ad74cd65292a4b384ba615214f684a5d5f22fbf83d5cceaa86f3ac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.bios.2004.06.040$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16511499$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15626618$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aoyagi, Satoka</creatorcontrib><creatorcontrib>Kudo, Masahiro</creatorcontrib><title>Effective monitoring of protein reaction on glass plate surfaces by TOF-SIMS</title><title>Biosensors & bioelectronics</title><addtitle>Biosens Bioelectron</addtitle><description>Time-of-flight secondary ion mass spectrometry (TOF-SIMS) is capable of chemically visualizing proteins on insulated samples. Distribution of an immobilized probe protein, fluorescent-labeled protein A-immobilized on a glass plate, and that of a sample protein, immunogloblin G (IgG) in solution, reacting with protein A on the biosensor surface, were evaluated with TOF-SIMS (TFS-2100, Physical Electronics). TOF-SIMS spectra and images of the protein on the glass plates were obtained, and this “mutual information”, as defined by information theory, was employed to analyze the TOF-SIMS spectra of proteins. Fragment ions from protein A and IgG were distinguished by the mutual, reinforcing information and specific fragment ions to each protein were selected to obtain the TOF-SIMS image of the protein. It is evident from the TOF-SIMS images of each protein that protein A was immobilized on the substrate homogeneously and that the reaction between the immobilized protein A and IgG is not localized in this condition. Chemical images of the proteins by TOF-SIMS will contribute to a better understanding of the reaction on the biosensor surface, and thus will help the development of more sophisticated biosensors. In addition, the requisite chemical conditions as well as the interaction between the biosensor surface and the immobilized proteins were investigated by TOF-SIMS by means of sets of reinforcing, mutually supportive information.</description><subject>Adsorption</subject><subject>Antigen-Antibody Complex - analysis</subject><subject>Antigen-Antibody Complex - chemistry</subject><subject>Antigen-Antibody Complex - immunology</subject><subject>Antigen-Antibody Reactions - immunology</subject><subject>Biological and medical sciences</subject><subject>Biosensing Techniques - instrumentation</subject><subject>Biosensing Techniques - methods</subject><subject>Biosensors</subject><subject>Biotechnology</subject><subject>Chemical imaging</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glass - chemistry</subject><subject>Immunoassay - instrumentation</subject><subject>Immunoassay - methods</subject><subject>Immunoglobulin G - analysis</subject><subject>Immunoglobulin G - chemistry</subject><subject>Immunoglobulin G - immunology</subject><subject>Information entropy</subject><subject>Mass Spectrometry - instrumentation</subject><subject>Mass Spectrometry - methods</subject><subject>Methods. Procedures. Technologies</subject><subject>Protein</subject><subject>Protein Binding</subject><subject>Protein Interaction Mapping - instrumentation</subject><subject>Protein Interaction Mapping - methods</subject><subject>Reproducibility of Results</subject><subject>Sensitivity and Specificity</subject><subject>Staphylococcal Protein A - analysis</subject><subject>Staphylococcal Protein A - chemistry</subject><subject>Staphylococcal Protein A - immunology</subject><subject>TOF-SIMS</subject><subject>Various methods and equipments</subject><issn>0956-5663</issn><issn>1873-4235</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1r3DAQhkVoSTZp_0APRZf2ZlefYxl6KSFJA1tySHoWY1kKWrzWVvIG8u-rZRdya2FgDvO8w_AMIZ84aznj8G3TDjGVVjCmWgYtU-yMrLjpZKOE1O_IivUaGg0gL8hlKRvGWMd7dk4uuAYBwM2KrG9C8G6JL55u0xyXlOP8TFOgu5wWH2eaPdZxmmmt5wlLobsJF0_LPgd0vtDhlT493DaP978eP5D3AafiP576Ffl9e_N0_bNZP9zdX_9YN04ZvjS9MiEAirHHsVNuBC16gWqQRg0IXAuuAhiFetRBiDAEI0ftnEc0ECQ6eUW-HvfWI__sfVnsNhbnpwlnn_bFQielkT38F-SdMmCMqaA4gi6nUrIPdpfjFvOr5cweZNuNPci2B9mWga2ya-jzaft-2PrxLXKyW4EvJwCLwylknF0sbxxozlXfV-77kfNV2kv02RYX_ez8GHN9jh1T_NcdfwEgBp0W</recordid><startdate>20050215</startdate><enddate>20050215</enddate><creator>Aoyagi, Satoka</creator><creator>Kudo, Masahiro</creator><general>Elsevier B.V</general><general>Elsevier Science</general><scope>IQODW</scope><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20050215</creationdate><title>Effective monitoring of protein reaction on glass plate surfaces by TOF-SIMS</title><author>Aoyagi, Satoka ; Kudo, Masahiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c481t-948ff6a2d9ad74cd65292a4b384ba615214f684a5d5f22fbf83d5cceaa86f3ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adsorption</topic><topic>Antigen-Antibody Complex - analysis</topic><topic>Antigen-Antibody Complex - chemistry</topic><topic>Antigen-Antibody Complex - immunology</topic><topic>Antigen-Antibody Reactions - immunology</topic><topic>Biological and medical sciences</topic><topic>Biosensing Techniques - instrumentation</topic><topic>Biosensing Techniques - methods</topic><topic>Biosensors</topic><topic>Biotechnology</topic><topic>Chemical imaging</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glass - chemistry</topic><topic>Immunoassay - instrumentation</topic><topic>Immunoassay - methods</topic><topic>Immunoglobulin G - analysis</topic><topic>Immunoglobulin G - chemistry</topic><topic>Immunoglobulin G - immunology</topic><topic>Information entropy</topic><topic>Mass Spectrometry - instrumentation</topic><topic>Mass Spectrometry - methods</topic><topic>Methods. Procedures. Technologies</topic><topic>Protein</topic><topic>Protein Binding</topic><topic>Protein Interaction Mapping - instrumentation</topic><topic>Protein Interaction Mapping - methods</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><topic>Staphylococcal Protein A - analysis</topic><topic>Staphylococcal Protein A - chemistry</topic><topic>Staphylococcal Protein A - immunology</topic><topic>TOF-SIMS</topic><topic>Various methods and equipments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aoyagi, Satoka</creatorcontrib><creatorcontrib>Kudo, Masahiro</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biosensors & bioelectronics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aoyagi, Satoka</au><au>Kudo, Masahiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effective monitoring of protein reaction on glass plate surfaces by TOF-SIMS</atitle><jtitle>Biosensors & bioelectronics</jtitle><addtitle>Biosens Bioelectron</addtitle><date>2005-02-15</date><risdate>2005</risdate><volume>20</volume><issue>8</issue><spage>1626</spage><epage>1630</epage><pages>1626-1630</pages><issn>0956-5663</issn><eissn>1873-4235</eissn><abstract>Time-of-flight secondary ion mass spectrometry (TOF-SIMS) is capable of chemically visualizing proteins on insulated samples. Distribution of an immobilized probe protein, fluorescent-labeled protein A-immobilized on a glass plate, and that of a sample protein, immunogloblin G (IgG) in solution, reacting with protein A on the biosensor surface, were evaluated with TOF-SIMS (TFS-2100, Physical Electronics). TOF-SIMS spectra and images of the protein on the glass plates were obtained, and this “mutual information”, as defined by information theory, was employed to analyze the TOF-SIMS spectra of proteins. Fragment ions from protein A and IgG were distinguished by the mutual, reinforcing information and specific fragment ions to each protein were selected to obtain the TOF-SIMS image of the protein. It is evident from the TOF-SIMS images of each protein that protein A was immobilized on the substrate homogeneously and that the reaction between the immobilized protein A and IgG is not localized in this condition. Chemical images of the proteins by TOF-SIMS will contribute to a better understanding of the reaction on the biosensor surface, and thus will help the development of more sophisticated biosensors. In addition, the requisite chemical conditions as well as the interaction between the biosensor surface and the immobilized proteins were investigated by TOF-SIMS by means of sets of reinforcing, mutually supportive information.</abstract><cop>Lausanne</cop><pub>Elsevier B.V</pub><pmid>15626618</pmid><doi>10.1016/j.bios.2004.06.040</doi><tpages>5</tpages></addata></record> |
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subjects | Adsorption Antigen-Antibody Complex - analysis Antigen-Antibody Complex - chemistry Antigen-Antibody Complex - immunology Antigen-Antibody Reactions - immunology Biological and medical sciences Biosensing Techniques - instrumentation Biosensing Techniques - methods Biosensors Biotechnology Chemical imaging Fundamental and applied biological sciences. Psychology Glass - chemistry Immunoassay - instrumentation Immunoassay - methods Immunoglobulin G - analysis Immunoglobulin G - chemistry Immunoglobulin G - immunology Information entropy Mass Spectrometry - instrumentation Mass Spectrometry - methods Methods. Procedures. Technologies Protein Protein Binding Protein Interaction Mapping - instrumentation Protein Interaction Mapping - methods Reproducibility of Results Sensitivity and Specificity Staphylococcal Protein A - analysis Staphylococcal Protein A - chemistry Staphylococcal Protein A - immunology TOF-SIMS Various methods and equipments |
title | Effective monitoring of protein reaction on glass plate surfaces by TOF-SIMS |
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