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Membrane Interactions of Antimicrobial Peptide-Loaded Microgels

Nordström, Randi (författare)
Uppsala University,Uppsala universitet,Institutionen för farmaci,farmaceutisk fysikalisk kemi
Browning, Kathryn L. (författare)
Uppsala University,Uppsala universitet,Institutionen för farmaci,Univ Copenhagen, Dept Pharm, DK-2100 Copenhagen, Denmark,University of Copenhagen
Parra-Ortiz, Elisa (författare)
Univ Copenhagen, Dept Pharm, DK-2100 Copenhagen, Denmark,University of Copenhagen
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Dangaard, Liv Sofia Elinor (författare)
Univ Copenhagen, Dept Pharm, DK-2100 Copenhagen, Denmark,University of Copenhagen
Malekkhaiat-Häffner, Sara (författare)
Univ Copenhagen, Dept Pharm, DK-2100 Copenhagen, Denmark,University of Copenhagen
Maestro, Armando (författare)
Inst Laue Langevin, F-38042 Grenoble 9, France,Institut Laue Langevin
Campbell, Richard A. (författare)
Inst Laue Langevin, F-38042 Grenoble 9, France;Univ Manchester, Div Pharm & Optometry, Manchester M13 9PT, Lancs, England,Institut Laue Langevin
Cooper, Joshaniel F. K. (författare)
Rutherford Appleton Lab, ISIS, Pulsed Neutron & Muon Source, Harwell OX11 0QX, Oxon, England,ISIS Neutron and Muon Source
Malmsten, Martin (författare)
Lund University,Lunds universitet,Fysikalisk kemi,Enheten för fysikalisk och teoretisk kemi,Kemiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Physical Chemistry,Physical and theoretical chemistry,Department of Chemistry,Departments at LTH,Faculty of Engineering, LTH,University of Copenhagen
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 (creator_code:org_t)
Elsevier BV, 2020
2020
Engelska.
Ingår i: Journal of Colloid and Interface Science. - : Elsevier BV. - 0021-9797 .- 1095-7103. ; 562, s. 322-332
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • In the present study, lipid membrane interactions of anionic poly(ethyl acrylate-co-methacrylic acid) (MAA) microgels as carriers for the cationic antimicrobial peptide LL-37 (LLGDFFRKSKEKIGKEFKRIVQRIKDFLRNLVPRTES) were investigated. In doing so, neutron reflectometry (NR), Fourier-transform infrared spectroscopy with attenuated total reflection (FTIR-ATR), zeta potential, ellipsometry, and circular dichroism spectroscopy (CD) experiments were employed to investigate the relative importance of membrane interactions of peptide-loaded microgel particles and of released peptide. For the free peptide, NR results showed membrane binding occurring preferentially in the tail region in a concentration-dependent manner. At low peptide concentration (0.3 mu M) only peptide insertion in the outer leaflet was seen, however, pronounced membrane defects and peptide present in both leaflets was observed at higher peptide concentration (5.0 LL-37 loaded into MAA microgels qualitatively mirrored these effects regarding both peptide localization within the membrane and concentration dependent defect formation. In addition, very limited membrane binding of microgel particles was observed, in agreement with FTIR-ATR and liposome leakage results. FTIR-ATR showed LL-37 to undergo alpha-helix formation on membrane insertion, also supported by CD results, the kinetics of which was substantially reduced for microgel-loaded LL-37 due to sustained peptide release. Together, these findings demonstrate that membrane interactions for microgel-loaded LL-37 are dominated by released peptide, but also that slow release of microgel-loaded LL-37 translates into kinetic effects on peptide-membrane interactions, relating to both peptide localization within the bilayer, and to bilayer structure.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)

Nyckelord

antimicrobial peptide
bilayer
membrane
microgel
neutron reflectometry
Pharmaceutical Physical Chemistry
Farmaceutisk fysikalisk kemi
Antimicrobial peptide
Bilayer
Membrane
Microgel
Neutron reflectometry

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