dc.creatorDOMINGUES, Marco M.
dc.creatorSANTIAGO, Patricia S.
dc.creatorCASTANHO, Miguel A. R. B.
dc.creatorSANTOS, Nuno C.
dc.date.accessioned2012-10-20T05:35:02Z
dc.date.accessioned2018-07-04T15:52:17Z
dc.date.available2012-10-20T05:35:02Z
dc.date.available2018-07-04T15:52:17Z
dc.date.created2012-10-20T05:35:02Z
dc.date.issued2008
dc.identifierJOURNAL OF PEPTIDE SCIENCE, v.14, n.4, p.394-400, 2008
dc.identifier1075-2617
dc.identifierhttp://producao.usp.br/handle/BDPI/31906
dc.identifier10.1002/psc.1007
dc.identifierhttp://dx.doi.org/10.1002/psc.1007
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1628544
dc.description.abstractHighly charged peptides are important components of the immune system and belong to an important family of antibiotics. Although their therapeutic activity is known, most of the molecular level mechanisms are controversial. A wide variety of different approaches are usually applied to understand their mechanisms, but light scattering techniques are frequently overlooked. Yet, light scattering is a noninvasive technique that allows insights both on the peptide mechanism of action as well as on the development of new antibiotics. Dynamic light scattering (DLS) and static light scattering (SLS) are used to measure the aggregation process of lipid vesicles upon addition of peptides and molecular properties (shape, molecular weight). The high charge of these peptides allows electrostatic attraction toward charged lipid vesicles, which is studied by zeta potential (zeta-potential) measurements. Copyright (c) 2008 European Peptide Society and John Wiley & Sons, Ltd.
dc.languageeng
dc.publisherJOHN WILEY & SONS LTD
dc.relationJournal of Peptide Science
dc.rightsCopyright JOHN WILEY & SONS LTD
dc.rightsrestrictedAccess
dc.subjectdynamic light scattering
dc.subjectstatic light scattering
dc.subjectzeta-potential
dc.subjecttherapeutic peptides
dc.titleWhat can light scattering spectroscopy do for membrane-active peptide studies
dc.typeArtículos de revistas


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