Show simple item record

dc.contributor.authorCândido, Elizabete S
dc.contributor.authorCardoso, Marlon H
dc.contributor.authorChan, Lai Y
dc.contributor.authorTorres, Marcelo DT
dc.contributor.authorOshiro, Karen GN
dc.contributor.authorPorto, William F
dc.contributor.authorRibeiro, Suzana M
dc.contributor.authorHaney, Evan F
dc.contributor.authorHancock, Robert EW
dc.contributor.authorLu, Timothy K
dc.contributor.authorde la Fuente-Nunez, Cesar
dc.contributor.authorCraik, David J
dc.contributor.authorFranco, Octávio L
dc.date.accessioned2021-10-27T20:34:18Z
dc.date.available2021-10-27T20:34:18Z
dc.date.issued2019
dc.identifier.urihttps://hdl.handle.net/1721.1/136219
dc.description.abstractCopyright © 2019 American Chemical Society. Bacterial biofilms and associated infections represent one of the biggest challenges in the clinic, and as an alternative to counter bacterial infections, antimicrobial peptides have attracted great attention in the past decade. Here, ten short cationic antimicrobial peptides were generated through a sliding-window strategy on the basis of the 19-amino acid residue peptide, derived from a Pyrobaculum aerophilum ribosomal protein. PaDBS1R6F10 exhibited anti-infective potential as it decreased the bacterial burden in murine Pseudomonas aeruginosa cutaneous infections by more than 1000-fold. Adverse cytotoxic and hemolytic effects were not detected against mammalian cells. The peptide demonstrated structural plasticity in terms of its secondary structure in the different environments tested. PaDBS1R6F10 represents a promising antimicrobial agent against bacteria infections, without harming human cells.
dc.language.isoen
dc.publisherAmerican Chemical Society (ACS)
dc.relation.isversionof10.1021/acsinfecdis.9b00073
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
dc.sourceACS
dc.titleShort Cationic Peptide Derived from Archaea with Dual Antibacterial Properties and Anti-Infective Potential
dc.typeArticle
dc.contributor.departmentMassachusetts Institute of Technology. Synthetic Biology Center
dc.contributor.departmentMassachusetts Institute of Technology. Center for Microbiome Informatics and Therapeutics
dc.contributor.departmentMassachusetts Institute of Technology. Research Laboratory of Electronics
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Science
dc.relation.journalACS Infectious Diseases
dc.eprint.versionAuthor's final manuscript
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2019-06-13T14:02:59Z
dspace.orderedauthorsCândido, ES; Cardoso, MH; Chan, LY; Torres, MDT; Oshiro, KGN; Porto, WF; Ribeiro, SM; Haney, EF; Hancock, REW; Lu, TK; de la Fuente-Nunez, C; Craik, DJ; Franco, OL
dspace.date.submission2019-06-13T14:03:00Z
mit.journal.volume5
mit.journal.issue7
mit.licensePUBLISHER_POLICY
mit.metadata.statusAuthority Work and Publication Information Needed


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record