Many-body effect of antimicrobial peptides: on the correlation between lipid's spontaneous curvature and pore formation - Wikidata - awgldk - TriplyDB

Many-body effect of antimicrobial peptides: on the correlation between lipid's spontaneous curvature and pore formation

Many-body effect of antimicrobial peptides: on the correlation between lipid's spontaneous curvature and pore formation

http://www.wikidata.org/entity/Q34352457

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Mechanisms of cellular uptake of cell-penetrating peptides Non-metabolic membrane tubulation and permeability induced by bioactive peptides Antimicrobial peptides temporins B and L induce formation of tubular lipid protrusions from supported phospholipid bilayers Process of inducing pores in membranes by melittin Localized permeabilization of E. coli membranes by the antimicrobial peptide Cecropin A.Interaction of an amphipathic peptide with phosphatidycholine/phosphatidylethanolamine mixed membranes Alamethicin aggregation in lipid membranes.The SV40 late protein VP4 is a viroporin that forms pores to disrupt membranes for viral release.Structure and water permeability of fully hydrated diphytanoylPC.SV40 late protein VP4 forms toroidal pores to disrupt membranes for viral release.The effect of membrane curvature on the conformation of antimicrobial peptides: implications for binding and the mechanism of action.Studying antibiotic-membrane interactions via X-ray diffraction and fluorescence microscopy The Simian virus 40 late viral protein VP4 disrupts the nuclear envelope for viral release.Membrane permeability of hydrocarbon-cross-linked peptides Cell-penetrating peptides: Possible transduction mechanisms and therapeutic applications.H-ras protein in a bilayer: interaction and structure perturbation The activity of the amphipathic peptide delta-lysin correlates with phospholipid acyl chain structure and bilayer elastic properties.Analysis of SARS-CoV E protein ion channel activity by tuning the protein and lipid charge.Mechanism of a prototypical synthetic membrane-active antimicrobial: Efficient hole-punching via interaction with negative intrinsic curvature lipids.Interaction of tea catechin (-)-epigallocatechin gallate with lipid bilayers.Free energies of molecular bound states in lipid bilayers: lethal concentrations of antimicrobial peptides Kinetic Defects Induced by Melittin in Model Lipid Membranes: A Solution Atomic Force Microscopy Study.Structure and Function of AApeptides.Resolving the kinetics of lipid, protein and peptide diffusion in membranes.Cell-penetrating peptides as a novel transdermal drug delivery system.The secrets of the Bcl-2 family.Cationic cell-penetrating peptides as vehicles for siRNA delivery.Interaction of LL-37 with model membrane systems of different complexity: influence of the lipid matrix.Antimicrobial and cell-penetrating peptides induce lipid vesicle fusion by folding and aggregation.Diffusion as a probe of the heterogeneity of antimicrobial peptide-membrane interactions.Thermodynamic profiling of peptide membrane interactions by isothermal titration calorimetry: a search for pores and micelles.Melittin-lipid bilayer interactions and the role of cholesterol.Backbone dynamics of alamethicin bound to lipid membranes: spin-echo electron paramagnetic resonance of TOAC-spin labels.Intramembrane water associated with TOAC spin-labeled alamethicin: electron spin-echo envelope modulation by D2O.Aggregatibacter actinomycetemcomitans leukotoxin cytotoxicity occurs through bilayer destabilization.Understanding membrane-active antimicrobial peptides.Effect of lipid shape on toroidal pore formation and peptide orientation in lipid bilayers.Transporting carriers for intracellular targeting delivery via non-endocytic uptake pathways.Computational investigations of pore forming peptide assemblies in lipid bilayers.Water channel formation and ion transport in linear and branched lipid bilayers.

P2860

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P2860

Many-body effect of antimicrobial peptides: on the correlation between lipid's spontaneous curvature and pore formation

http://www.wikidata.org/entity/Q34352457

description

2005 nî lūn-bûn

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2005 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2005 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2005年の論文

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2005年論文

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2005年論文

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2005年论文

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Many-body effect of antimicrob ...... s curvature and pore formation

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Many-body effect of antimicrob ...... s curvature and pore formation

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Many-body effect of antimicrob ...... s curvature and pore formation

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BIOPHYSJ.105.068080

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Biophysical Journal

P1476

Many-body effect of antimicrob ...... s curvature and pore formation

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P2093

Fang-Yu Chen

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Huey W Huang

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Ming-Tao Lee

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Wei-Chin Hung

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P2860

Effect of chain length and unsaturation on elasticity of lipid bilayers.

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

Structure of lipid bilayers

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

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

The structure of melittin in the form I crystals and its implication for melittin's lytic and surface activities.

Orientation and dynamics of an antimicrobial peptide in the lipid bilayer by solid-state NMR spectroscopy.

Membrane binding and pore formation of the antibacterial peptide PGLa: thermodynamic and mechanistic aspects.

Theoretical analysis of hydrophobic matching and membrane-mediated interactions in lipid bilayers containing gramicidin.

Interaction of antimicrobial peptides with biological and model membranes: structural and charge requirements for activity.

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10.1529/BIOPHYSJ.105.068080

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6

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89

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16150963

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1366966

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