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Publicação:
Tethered DNA scaffolds on optical sensor platforms for detection of hipO gene from Campylobacter jejuni

dc.contributor.authorGnanaprakasa, Tony J.
dc.contributor.authorOyarzabal, Omar A.
dc.contributor.authorOlsen, Eric V.
dc.contributor.authorPedrosa, Valber A. [UNESP]
dc.contributor.authorSimonian, Aleksandr L.
dc.contributor.institutionAuburn University (AU)
dc.contributor.institutionAlabama State University (ASU)
dc.contributor.institutionKeesler Air Force Base
dc.contributor.institutionUniversity of Arizona
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:25:57Z
dc.date.available2014-05-27T11:25:57Z
dc.date.issued2011-08-10
dc.description.abstractDNA biosensors have gained increased attention over traditional diagnostic methods due to their fast and responsive operation and cost-effective design. The specificity of DNA biosensors relies on single-stranded oligonucleotide probes immobilized to a transduction platform. Here, we report the development of biosensors to detect the hippuricase gene (hipO) from Campylobacter jejuni using direct covalent coupling of thiol- and biotin-labeled single-stranded DNA (ssDNA) on both surface plasmon resonance (SPR) and diffraction optics technology (DOT, dotLab) transduction platforms. This is the first known report of the dotLab to detect targeted DNA. Application of 6-mercapto-1-hexanol as a spacer thiol for SPR gold surface created a self-assembled monolayer that removed unbound ssDNA and minimized non-specific detection. The detection limit of SPR sensors was shown to be 2.5 nM DNA while dotLab sensors demonstrated a slightly decreased detection limit of 5.0 nM (0.005 μM). It was possible to reuse the SPR sensor due to the negligible changes in sensor sensitivity (∼9.7 × 10 -7 ΔRU) and minimal damage to immobilized probes following use, whereas dotLab sensors could not be reused. Results indicated feasibility of optical biosensors for rapid and sensitive detection of the hipO gene of Campylobacter jejuni using specific ssDNA as a probe. © 2011 Elsevier B.V.en
dc.description.affiliationMaterials Research and Education Center Samuel Ginn College of Engineering Auburn University, 275 Wilmore Laboratories, AL 36849
dc.description.affiliationDepartment of Biological Sciences Alabama State University, Montgomery, AL 36104
dc.description.affiliationClinical Research Laboratory 81st Medical Group, Keesler Air Force Base, Biloxi, MS 39534
dc.description.affiliationDepartment of Materials Science and Engineering University of Arizona, Tucson, AZ
dc.description.affiliationInstitute of Bioscience Department of Chemistry and Biochemistry UNESP, Botucatu, SP
dc.description.affiliationUnespInstitute of Bioscience Department of Chemistry and Biochemistry UNESP, Botucatu, SP
dc.format.extent304-311
dc.identifierhttp://dx.doi.org/10.1016/j.snb.2011.04.037
dc.identifier.citationSensors and Actuators, B: Chemical, v. 156, n. 1, p. 304-311, 2011.
dc.identifier.doi10.1016/j.snb.2011.04.037
dc.identifier.issn0925-4005
dc.identifier.lattes7781282422851911
dc.identifier.scopus2-s2.0-79957849081
dc.identifier.urihttp://hdl.handle.net/11449/72595
dc.language.isoeng
dc.relation.ispartofSensors and Actuators B: Chemical
dc.relation.ispartofjcr5.667
dc.relation.ispartofsjr1,406
dc.rights.accessRightsAcesso restrito
dc.sourceScopus
dc.subjectCampylobacter jejuni
dc.subjectDiffraction optics technology
dc.subjectdotLab
dc.subjecthipO gene
dc.subjectLabel-free DNA detection
dc.subjectSelf-assembled monolayers
dc.subjectSPR
dc.subjectSPREETA
dc.subjectDiffraction optics
dc.subjectLabel free
dc.subjectBacteriophages
dc.subjectBiosensors
dc.subjectDiffraction
dc.subjectElectron energy levels
dc.subjectGenes
dc.subjectOligonucleotides
dc.subjectOrganic polymers
dc.subjectProbes
dc.subjectScaffolds
dc.subjectSelf assembled monolayers
dc.subjectSensors
dc.subjectSurface plasmon resonance
dc.subjectDNA
dc.titleTethered DNA scaffolds on optical sensor platforms for detection of hipO gene from Campylobacter jejunien
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dspace.entity.typePublication
unesp.author.lattes7781282422851911
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.departmentQuímica e Bioquímica - IBBpt

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