dc.creatorBarreto-Santamaría A.
dc.creatorPatarroyo M.E.
dc.creatorCurtidor H.
dc.date.accessioned2020-05-26T00:05:20Z
dc.date.accessioned2022-09-22T14:32:06Z
dc.date.available2020-05-26T00:05:20Z
dc.date.available2022-09-22T14:32:06Z
dc.date.created2020-05-26T00:05:20Z
dc.identifier10408363
dc.identifier1549781X
dc.identifierhttps://repository.urosario.edu.co/handle/10336/23781
dc.identifierhttps://doi.org/10.1080/10408363.2019.1631249
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3439765
dc.description.abstractBecause the resistance of microorganisms to the available antibiotics is a growing healthcare problem worldwide, the search for new antimicrobial peptides (AMPs) that provide useful therapeutic options has been increasing in importance. Many initial candidates have had to be discarded after having advanced to the preclinical and clinical stages. This has led to substantial losses in terms of time and money. For that reason, the essential characteristics of AMPs (i.e. their activity, selectivity, stability in physiological conditions and low production cost) must be considered in their design. In addition, peptides could be active against several kinds of cells with activity and selectivity resulting from interaction with multiple target cell components, which sometimes are present in mammalian cells as well. Thus, the cellular composition is important in the AMP-target cell interaction and must be considered in the design of AMPs, too. This review describes general aspects of AMP design, limitations concerning their therapeutic application, and optimization strategies for overcoming such limitations. © 2019, © 2019 Informa UK Limited, trading as Taylor and Francis Group.
dc.languageeng
dc.publisherTaylor and Francis Ltd
dc.relationCritical Reviews in Clinical Laboratory Sciences, ISSN:10408363, 1549781X, Vol.56, No.6 (2019); pp. 351-373
dc.relationhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85070523024&doi=10.1080%2f10408363.2019.1631249&partnerID=40&md5=133160fd7b211c0acc3384c1e0f1ba0a
dc.relation373
dc.relationNo. 6
dc.relation351
dc.relationCritical Reviews in Clinical Laboratory Sciences
dc.relationVol. 56
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightsAbierto (Texto Completo)
dc.sourceinstname:Universidad del Rosario
dc.sourcereponame:Repositorio Institucional EdocUR
dc.titleDesigning and optimizing new antimicrobial peptides: all targets are not the same
dc.typearticle


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