Membrane thinning due to antimicrobial peptide binding: an atomic force microscopy study of MSI-78 in lipid bilayers. - Wikidata - awgldk - TriplyDB

Membrane thinning due to antimicrobial peptide binding: an atomic force microscopy study of MSI-78 in lipid bilayers.

Membrane thinning due to antimicrobial peptide binding: an atomic force microscopy study of MSI-78 in lipid bilayers.

http://www.wikidata.org/entity/Q34352478

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Conformational study of the protegrin-1 (PG-1) dimer interaction with lipid bilayers and its effect Studies on anticancer activities of antimicrobial peptides Antimicrobial peptides Interaction of the antimicrobial peptide polymyxin B1 with both membranes of E. coli: a molecular dynamics study Solid-state ¹³C NMR reveals annealing of raft-like membranes containing cholesterol by the intrinsically disordered protein α-Synuclein Formation and Characterization of Supported Lipid Bilayers Composed of Hydrogenated and Deuterated Escherichia coli Lipids.Multiscale observation of biological interactions of nanocarriers: from nano to macro.Antimicrobial peptides temporins B and L induce formation of tubular lipid protrusions from supported phospholipid bilayers Real-time measurement of membrane conformational states induced by antimicrobial peptides: balance between recovery and lysis.Deletion of all cysteines in tachyplesin I abolishes hemolytic activity and retains antimicrobial activity and lipopolysaccharide selective binding Membrane Thinning and Thickening Induced by Membrane-Active Amphipathic Peptides.Modular determinants of antimicrobial activity in platelet factor-4 family kinocidins.Interaction of the Antimicrobial Peptide Aurein 1.2 and Charged Lipid Bilayer.Driving engineering of novel antimicrobial peptides from simulations of peptide-micelle interactions.Antimicrobial protegrin-1 forms ion channels: molecular dynamic simulation, atomic force microscopy, and electrical conductance studies The Photodynamic Effect of Different Size ZnO Nanoparticles on Cancer Cell Proliferation In Vitro Synergistic Effect of Functionalized Nickel Nanoparticles and Quercetin on Inhibition of the SMMC-7721 Cells Proliferation.Effect of antimicrobial peptide-amide: indolicidin on biological membranes.Solid-state NMR investigation of the membrane-disrupting mechanism of antimicrobial peptides MSI-78 and MSI-594 derived from magainin 2 and melittin.Transmembrane pores formed by human antimicrobial peptide LL-37.Interaction of protegrin-1 with lipid bilayers: membrane thinning effect.Membrane orientation of MSI-78 measured by sum frequency generation vibrational spectroscopy.Membrane insertion and bilayer perturbation by antimicrobial peptide CM15.Does cholesterol suppress the antimicrobial peptide induced disruption of lipid raft containing membranes?The role of ganglioside GM1 in cellular internalization mechanisms of poly(amidoamine) dendrimers.Current state of a dual behaviour of antimicrobial peptides-Therapeutic agents and promising delivery vectors.Crabrolin, a natural antimicrobial peptide: structural properties.Quantitative Measurement of Cationic Polymer Vector and Polymer-pDNA Polyplex Intercalation into the Cell Plasma Membrane.Nanoparticle interaction with biological membranes: does nanotechnology present a Janus face?A high-resolution solid-state NMR approach for the structural studies of bicelles H-ras protein in a bilayer: interaction and structure perturbation Nanoscale imaging reveals laterally expanding antimicrobial pores in lipid bilayers.Models of toxic beta-sheet channels of protegrin-1 suggest a common subunit organization motif shared with toxic alzheimer beta-amyloid ion channels.Evaluation of a lipopeptide biosurfactant from Bacillus natto TK-1 as a potential source of anti-adhesive, antimicrobial and antitumor activities.Beyond NMR spectra of antimicrobial peptides: dynamical images at atomic resolution and functional insights.Effect of membrane composition on antimicrobial peptides aurein 2.2 and 2.3 from Australian southern bell frogs Structure, membrane orientation, mechanism, and function of pexiganan--a highly potent antimicrobial peptide designed from magainin.Molecular interactions between magainin 2 and model membranes in situ Detergent induction of HEK 293A cell membrane permeability measured under quiescent and superfusion conditions using whole cell patch clamp Antimicrobial peptides: key components of the innate immune system.

P2860

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P2860

Membrane thinning due to antimicrobial peptide binding: an atomic force microscopy study of MSI-78 in lipid bilayers.

http://www.wikidata.org/entity/Q34352478

description

2005 nî lūn-bûn

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BIOPHYSJ.105.062596

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Biophysical Journal

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Membrane thinning due to antim ...... dy of MSI-78 in lipid bilayers

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Almut Mecke

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Bradford G Orr

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Dong-Kuk Lee

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P2860

MSI-78, an analogue of the magainin antimicrobial peptides, disrupts lipid bilayer structure via positive curvature strain.

Magainins, a class of antimicrobial peptides from Xenopus skin: isolation, characterization of two active forms, and partial cDNA sequence of a precursor

A voltage-gated ion channel model inferred from the crystal structure of alamethicin at 1.5-A resolution

Antimicrobial peptides of multicellular organisms

Barrel-stave model or toroidal model? A case study on melittin pores.

Electric charge effects on phospholipid headgroups. Phosphatidylcholine in mixtures with cationic and anionic amphiphiles.

Lipid membrane phase behaviour elucidated in real time by controlled environment atomic force microscopy.

Membrane lateral compressibility determined by NMR and x-ray diffraction: effect of acyl chain polyunsaturation.

Neutron scattering in the plane of membranes: structure of alamethicin pores

Mechanism of alamethicin insertion into lipid bilayers.

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4043-4050

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10.1529/BIOPHYSJ.105.062596

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Ayyalusamy Ramamoorthy

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7580212

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16183881

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1366969

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