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dc.contributor.authorPeltomaa, Riikka
dc.contributor.authorBenito-Peña, Elena
dc.contributor.authorBarderas Manchado, Rodrigo 
dc.contributor.authorMoreno-Bondi, María C
dc.date.accessioned2020-02-21T12:56:40Z
dc.date.available2020-02-21T12:56:40Z
dc.date.issued2019-07-31
dc.identifier.citationACS Omega. 2019 Jul 3;4(7):11569-11580.es_ES
dc.identifier.issn2470-1343es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/9141
dc.description.abstractPhages are bacterial viruses that have gained a significant role in biotechnology owing to their widely studied biology and many advantageous characteristics. Perhaps the best-known application of phages is phage display that refers to the expression of foreign peptides or proteins outside the phage virion as a fusion with one of the phage coat proteins. In 2018, one half of the Nobel prize in chemistry was awarded jointly to George P. Smith and Sir Gregory P. Winter "for the phage display of peptides and antibodies." The outstanding technology has evolved and developed considerably since its first description in 1985, and today phage display is commonly used in a wide variety of disciplines, including drug discovery, enzyme optimization, biomolecular interaction studies, as well as biosensor development. A cornerstone of all biosensors, regardless of the sensor platform or transduction scheme used, is a sensitive and selective bioreceptor, or a recognition element, that can provide specific binding to the target analyte. Many environmentally or pharmacologically interesting target analytes might not have naturally appropriate binding partners for biosensor development, but phage display can facilitate the production of novel receptors beyond known biomolecular interactions, or against toxic or nonimmunogenic targets, making the technology a valuable tool in the quest of new recognition elements for biosensor development.es_ES
dc.description.sponsorshipThis study was supported by the Ministry of Economy and Competitiveness (Ministerio de Ciencia, Innovación y Universidades RTI2018-096410-B-C21). R.P. acknowledges UCM for a predoctoral grant and R.B. the PI17CIII/00045 grant from the AES-ISCIII program.es_ES
dc.language.isoenges_ES
dc.publisherAmerican Chemical Society (ACS) es_ES
dc.type.hasVersionVoRes_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.titlePhage Display in the Quest for New Selective Recognition Elements for Biosensorses_ES
dc.typejournal articlees_ES
dc.rights.licenseAtribución-NoComercial-CompartirIgual 4.0 Internacional*
dc.identifier.pubmedID31460264es_ES
dc.format.volume4es_ES
dc.format.number7es_ES
dc.format.page11569-11580es_ES
dc.identifier.doi10.1021/acsomega.9b01206es_ES
dc.contributor.funderMinisterio de Economía y Competitividad (España) 
dc.contributor.funderMinisterio de Ciencia, Innovación y Universidades (España) 
dc.contributor.funderInstituto de Salud Carlos III 
dc.description.peerreviewedes_ES
dc.identifier.e-issn2470-1343es_ES
dc.relation.publisherversionhttps://doi.org/10.1021/acsomega.9b01206es_ES
dc.identifier.journalACS omegaes_ES
dc.repisalud.centroISCIII::Unidad Funcional de Investigación de Enfermedades Crónicas (UFIEC)es_ES
dc.repisalud.institucionISCIIIes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RTI2018-096410-B-C21es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/PI17CIII/00045es_ES
dc.rights.accessRightsopen accesses_ES


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