dc.contributor.author | Peltomaa, Riikka | |
dc.contributor.author | Benito-Peña, Elena | |
dc.contributor.author | Barderas Manchado, Rodrigo | |
dc.contributor.author | Moreno-Bondi, María C | |
dc.date.accessioned | 2020-02-21T12:56:40Z | |
dc.date.available | 2020-02-21T12:56:40Z | |
dc.date.issued | 2019-07-31 | |
dc.identifier.citation | ACS Omega. 2019 Jul 3;4(7):11569-11580. | es_ES |
dc.identifier.issn | 2470-1343 | es_ES |
dc.identifier.uri | http://hdl.handle.net/20.500.12105/9141 | |
dc.description.abstract | Phages 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.sponsorship | This 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.iso | eng | es_ES |
dc.publisher | American Chemical Society (ACS) | es_ES |
dc.type.hasVersion | VoR | es_ES |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | * |
dc.title | Phage Display in the Quest for New Selective Recognition Elements for Biosensors | es_ES |
dc.type | journal article | es_ES |
dc.rights.license | Atribución-NoComercial-CompartirIgual 4.0 Internacional | * |
dc.identifier.pubmedID | 31460264 | es_ES |
dc.format.volume | 4 | es_ES |
dc.format.number | 7 | es_ES |
dc.format.page | 11569-11580 | es_ES |
dc.identifier.doi | 10.1021/acsomega.9b01206 | es_ES |
dc.contributor.funder | Ministerio de Economía y Competitividad (España) | |
dc.contributor.funder | Ministerio de Ciencia, Innovación y Universidades (España) | |
dc.contributor.funder | Instituto de Salud Carlos III | |
dc.description.peerreviewed | Sí | es_ES |
dc.identifier.e-issn | 2470-1343 | es_ES |
dc.relation.publisherversion | https://doi.org/10.1021/acsomega.9b01206 | es_ES |
dc.identifier.journal | ACS omega | es_ES |
dc.repisalud.centro | ISCIII::Unidad Funcional de Investigación de Enfermedades Crónicas (UFIEC) | es_ES |
dc.repisalud.institucion | ISCIII | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/ES/RTI2018-096410-B-C21 | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/ES/PI17CIII/00045 | es_ES |
dc.rights.accessRights | open access | es_ES |