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Smart Plastic Antibody Material (SPAM) tailored on disposable screen printed electrodes for protein recognition: application to Myoglobin detection

dc.contributor.authorMoreira, Felismina T. C.
dc.contributor.authorSharma, Sanjiv
dc.contributor.authorDutra, Rosa A.F.
dc.contributor.authorNoronha, João P. C.
dc.contributor.authorCass, Anthony E. G.
dc.contributor.authorSales, M. Goreti F.
dc.date.accessioned2015-10-19T08:49:32Z
dc.date.available2015-10-19T08:49:32Z
dc.date.issued2013
dc.description.abstractThis work introduces two major changes to the conventional protocol for designing plastic antibodies: (i) the imprinted sites were created with charged monomers while the surrounding environment was tailored using neutral material; and (ii) the protein was removed from its imprinted site by means of a protease, aiming at preserving the polymeric network of the plastic antibody. To our knowledge, these approaches were never presented before and the resulting material was named here as smart plastic antibody material (SPAM). As proof of concept, SPAM was tailored on top of disposable gold-screen printed electrodes (Au-SPE), following a bottom-up approach, for targeting myoglobin (Myo) in a point-of-care context. The existence of imprinted sites was checked by comparing a SPAM modified surface to a negative control, consisting of similar material where the template was omitted from the procedure and called non-imprinted materials (NIMs). All stages of the creation of the SPAM and NIM on the Au layer were followed by both electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). AFM imaging was also performed to characterize the topography of the surface. There are two major reasons supporting the fact that plastic antibodies were effectively designed by the above approach: (i) they were visualized for the first time by AFM, being present only in the SPAM network; and (ii) only the SPAM material was able to rebind to the target protein and produce a linear electrical response against EIS and square wave voltammetry (SWV) assays, with NIMs showing a similar-to-random behavior. The SPAM/Au-SPE devices displayed linear responses to Myo in EIS and SWV assays down to 3.5 μg/mL and 0.58 μg/mL, respectively, with detection limits of 1.5 and 0.28 μg/mL. SPAM materials also showed negligible interference from troponin T (TnT), bovine serum albumin (BSA) and urea under SWV assays, showing promising results for point-of-care applications when applied to spiked biological fluids.pt_PT
dc.identifier.doi10.1016/j.bios.2013.02.012
dc.identifier.urihttp://hdl.handle.net/10400.22/6732
dc.language.isoengpt_PT
dc.publisherElsevierpt_PT
dc.relation.publisherversionhttp://www.sciencedirect.com/science/article/pii/S0956566313001103pt_PT
dc.subjectPlastic antibodypt_PT
dc.subjectCharged binding sitept_PT
dc.subjectSurface-molecular imprintpt_PT
dc.subjectScreen-printed electrodespt_PT
dc.subjectMyoglobinpt_PT
dc.subjectBiosensorpt_PT
dc.titleSmart Plastic Antibody Material (SPAM) tailored on disposable screen printed electrodes for protein recognition: application to Myoglobin detectionpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage244pt_PT
oaire.citation.startPage237pt_PT
oaire.citation.titleBiosensors and Bioelectronicspt_PT
oaire.citation.volume45pt_PT
person.familyNameMoreira
person.givenNameFelismina
person.identifier1589429
person.identifier.ciencia-idC917-6A46-A270
person.identifier.orcid0000-0003-4237-8952
person.identifier.scopus-author-id23486193000
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublication9c13153d-a73a-49ff-b7f6-c9733bc6725e
relation.isAuthorOfPublication.latestForDiscovery9c13153d-a73a-49ff-b7f6-c9733bc6725e

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