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Study on the mechanism of Bioelectric Recognition Assay: Evidence for immobilized cell membrane interactions with viral fragments

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dc.contributor.author Kintzios, S en
dc.contributor.author Bem, F en
dc.contributor.author Mangana, O en
dc.contributor.author Nomikou, K en
dc.contributor.author Markoulatos, P en
dc.contributor.author Alexandropoulos, N en
dc.contributor.author Fasseas, C en
dc.contributor.author Arakelyan, V en
dc.contributor.author Petrou, A-L en
dc.contributor.author Soukouli, K en
dc.contributor.author Moschopoulou, G en
dc.contributor.author Yialouris, C en
dc.contributor.author Simonian, A en
dc.date.accessioned 2014-06-06T06:46:08Z
dc.date.available 2014-06-06T06:46:08Z
dc.date.issued 2004 en
dc.identifier.issn 09565663 en
dc.identifier.uri http://dx.doi.org/10.1016/j.bios.2004.04.009 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/2804
dc.subject Antibody en
dc.subject Bioelectric Recognition Assay (BERA) en
dc.subject Biosensor en
dc.subject Cell immobilization en
dc.subject Electrophysiological response en
dc.subject Herpes viruses en
dc.subject Plant viruses en
dc.subject Virus en
dc.subject.other Antibodies en
dc.subject.other Bioelectric phenomena en
dc.subject.other Biosensors en
dc.subject.other Cell immobilization en
dc.subject.other Cell membranes en
dc.subject.other Electrophysiology en
dc.subject.other Gels en
dc.subject.other Proteins en
dc.subject.other Viruses en
dc.subject.other Bioactivity en
dc.subject.other Bioelectric recognition assay (BERA) en
dc.subject.other Coat proteins en
dc.subject.other Ligands en
dc.subject.other Assays en
dc.subject.other coat protein en
dc.subject.other proteinase en
dc.subject.other virus antibody en
dc.subject.other amino acid sequence en
dc.subject.other article en
dc.subject.other bioenergy en
dc.subject.other cell interaction en
dc.subject.other electrophysiology en
dc.subject.other fluorescence analysis en
dc.subject.other gene sequence en
dc.subject.other immobilization en
dc.subject.other membrane potential en
dc.subject.other virus envelope en
dc.subject.other Animalia en
dc.subject.other Herpesviridae en
dc.title Study on the mechanism of Bioelectric Recognition Assay: Evidence for immobilized cell membrane interactions with viral fragments en
heal.type journalArticle en
heal.identifier.primary 10.1016/j.bios.2004.04.009 en
heal.publicationDate 2004 en
heal.abstract The Bioelectric Recognition Assay (BERA) is a whole-cell based biosensing system that detects the electric response of cultured cells, suspended in a gel matrix, to various ligands, which bind to the cell and/or affect its physiology. Previous studies have demonstrated the potential application of this method for rapid, inexpensive detection of viruses in a crude sample. However, the understanding, so far, of the fundamental processes that take place during cell-virus interactions within the probe has been rather limited. In the present study, we combined electrophysiological and fluorescence microscopical assays, so that we can prove that animal and plant cells immobilized in BERA sensors respond to different viruses primarily by changing their membrane potential. The response of immobilized cells against different viruses did not depend on the virus ability to penetrate the cell, but was modified after binding each virus to a virus-specific antibody or removal of its coat protein after treatment with a protease. Consequently, we were able to assay the presence of a virus in its complete form or fragments thereof. Combination of immunological recognition with the electrophysiological response of immobilized cells allows for a considerable increase of the specificity of the BERA biosensory assay. In addition, rather than simply detect the presence of a protein or genomic sequence, the method can help gain information on the bioactivity of a virus. © 2004 Elsevier B.V. All rights reserved. en
heal.journalName Biosensors and Bioelectronics en
dc.identifier.issue 4 en
dc.identifier.volume 20 en
dc.identifier.doi 10.1016/j.bios.2004.04.009 en
dc.identifier.spage 906 en
dc.identifier.epage 915 en


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