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Optimization of the aptamers’ immobilization conditions for maximizing the response of a dualaptasensor for cancer biomarker detection

dc.contributor.authorMeirinho, Sofia G.
dc.contributor.authorEzziddine, Maha
dc.contributor.authorVeloso, Ana C.A.
dc.contributor.authorDias, L.G.
dc.contributor.authorRodrigues, Lígia R.
dc.contributor.authorOthmane, Ali
dc.contributor.authorPeres, António M.
dc.date.accessioned2020-02-27T15:45:49Z
dc.date.available2020-02-27T15:45:49Z
dc.date.issued2017
dc.description.abstractOsteopontin (OPN) is a protein that is present in several body fluids and has been reported as a possible cancer biomarker, being its overexpression associated with tumour progression and metastasis [1,2]. A simple and sensitive method that allows the simultaneous detection of single or multiple cancer biomarkers is envisaged and may be an important tool in cancer diagnosis. In this work, two bioreceptors specific for OPN, a RNA aptamer (OPN-R3) previously described by Mi and co-workers [3] and a DNA aptamer (C10K2) developed by our research group, were biotinylated and immobilized on a dual-screen printed gold electrode through streptavidin-biotin interaction. The voltammetric signals generated by the dual-aptasensor array, after the formation of the aptamers-protein complex, were monitored using cyclic voltammetry (CV) and square- wave voltammetry (SWV), using [Fe(CN)6]−3/−4 as a redox probe. The optimal immobilization conditions for the dual-aptasensor array were established by response surface methodology. The maximum voltammetric response was obtained for a 0.5 μM aptamer concentration after 20 min of aptamers’ immobilization and 30 min of aptamer- OPN interaction time at an incubation temperature of 4ºC. The satisfactory preliminary results obtained, although needing further confirmation for synthetic or real human samples, point out that the proposed electrochemical dual-aptasensor array could be a simple and sensitive tool for the detection of OPN, as well as for other potential cancer biomarkers and therefore, may be applied in the future for cancer disease monitoring.pt_PT
dc.description.sponsorshipThis work was also financially supported by Project POCI-01–0145-FEDER-006984 – Associate Laboratory LSRE-LCM funded by FEDER through COMPETE2020 and by national funds through FCT, Portugal. S. Meirinho also acknowledges the research grant provided by Project UID/EQU/50020/2013.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationMeirinho, Sofia G.; Ezzedine, Maha; Veloso, Ana C.A.; Dias, L.G.; Rodrigues, Lígia R.; Othmane, Ali; Peres, António M. (2017). Optimization of the aptamers’ immobilization conditions for maximizing the response of a dualaptasensor for cancer biomarker detection. In XIV Reunión Ibernam. Tordesillaspt_PT
dc.identifier.urihttp://hdl.handle.net/10198/20739
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/pt_PT
dc.titleOptimization of the aptamers’ immobilization conditions for maximizing the response of a dualaptasensor for cancer biomarker detectionpt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/5876/UID%2FEQU%2F50020%2F2013/PT
oaire.citation.conferencePlaceTordesillas, Espanhapt_PT
oaire.citation.titleXIV Reunión IberNAMpt_PT
oaire.fundingStream5876
person.familyNameDias
person.familyNamePeres
person.givenNameLuís G.
person.givenNameAntónio M.
person.identifier107333
person.identifier.ciencia-id2F11-9092-FAAF
person.identifier.ciencia-idCF16-5443-F420
person.identifier.orcid0000-0002-1210-4259
person.identifier.orcid0000-0001-6595-9165
person.identifier.ridI-8470-2012
person.identifier.scopus-author-id23569169900
person.identifier.scopus-author-id7102331969
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT
relation.isAuthorOfPublicationeac8c166-4056-4ed0-8d8d-7ecb2c4481a5
relation.isAuthorOfPublication7d93be47-8dc4-4413-9304-5b978773d3bb
relation.isAuthorOfPublication.latestForDiscoveryeac8c166-4056-4ed0-8d8d-7ecb2c4481a5
relation.isProjectOfPublication66ec3fc3-043e-4147-a64b-3d87442cc076
relation.isProjectOfPublication.latestForDiscovery66ec3fc3-043e-4147-a64b-3d87442cc076

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