From "carpet" mechanism to de-novo designed diastereomeric cell-selective antimicrobial peptides.
about
Interaction of viscotoxins A3 and B with membrane model systems: implications to their mechanism of actionCationic membrane peptides: atomic-level insight of structure-activity relationships from solid-state NMROn the role of NMR spectroscopy for characterization of antimicrobial peptidesTreatment of microbial biofilms in the post-antibiotic era: prophylactic and therapeutic use of antimicrobial peptides and their design by bioinformatics toolsAntimicrobial peptides for therapeutic applications: a reviewControls and constrains of the membrane disrupting action of Aurein 1.2.Functional and structural characterization of a dense core secretory granule sorting domain from the PC1/3 proteaseDermaseptins from Phyllomedusa oreades and Phyllomedusa distincta. Anti-Trypanosoma cruzi activity without cytotoxicity to mammalian cellsContext mediates antimicrobial efficacy of kinocidin congener peptide RP-1The anti-angiogenic peptide anginex disrupts the cell membrane.Characterization of a potent antimicrobial lipopeptide via coarse-grained molecular dynamics.Specific and selective peptide-membrane interactions revealed using quartz crystal microbalance.Molecular dynamics simulations of a new branched antimicrobial peptide: a comparison of force fields.The antimicrobial mechanism of action of epsilon-poly-l-lysine.Molecular dynamics investigation of the influence of anionic and zwitterionic interfaces on antimicrobial peptides' structure: implications for peptide toxicity and activityRational combinatorial design of pore-forming beta-sheet peptides.Beta-sheet pore-forming peptides selected from a rational combinatorial library: mechanism of pore formation in lipid vesicles and activity in biological membranes.Peptoids that mimic the structure, function, and mechanism of helical antimicrobial peptides.Biomolecular engineering by combinatorial design and high-throughput screening: small, soluble peptides that permeabilize membranes.Transcriptome analysis of the responses of Staphylococcus aureus to antimicrobial peptides and characterization of the roles of vraDE and vraSR in antimicrobial resistance.Pardaxin permeabilizes vesicles more efficiently by pore formation than by disruptionDe novo design of antimicrobial polymers, foldamers, and small molecules: from discovery to practical applications.Simulating the mechanism of antimicrobial lipopeptides with all-atom molecular dynamics.Role of helicity of α-helical antimicrobial peptides to improve specificity.Broad-spectrum antimicrobial peptides by rational combinatorial design and high-throughput screening: the importance of interfacial activity.Lipid headgroup discrimination by antimicrobial peptide LL-37: insight into mechanism of action.Thermodynamics of antimicrobial lipopeptide binding to membranes: origins of affinity and selectivityHost defense peptides: an alternative as antiinfective and immunomodulatory therapeutics.Synthetic molecular evolution of pore-forming peptides by iterative combinatorial library screening.Ion channel formation and membrane-linked pathologies of misfolded hydrophobic proteins: the role of dangerous unchaperoned molecules.Toward the de novo design of antimicrobial peptides: Lack of correlation between peptide permeabilization of lipid vesicles and antimicrobial, cytolytic, or cytotoxic activity in living cells.De-novo design of antimicrobial peptides for plant protection.Antimicrobial peptides design by evolutionary multiobjective optimizationN-acylated peptides derived from human lactoferricin perturb organization of cardiolipin and phosphatidylethanolamine in cell membranes and induce defects in Escherichia coli cell division.Ultrashort antibacterial and antifungal lipopeptidesThe role of antimicrobial peptides in preventing multidrug-resistant bacterial infections and biofilm formation.Membrane-Active Small Molecules: Designs Inspired by Antimicrobial Peptides.Conformational Fine-Tuning of Pore-Forming Peptide Potency and Selectivity.Reorientation and dimerization of the membrane-bound antimicrobial peptide PGLa from microsecond all-atom MD simulations.pH-Triggered, Macromolecule-Sized Poration of Lipid Bilayers by Synthetically Evolved Peptides.
P2860
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P2860
From "carpet" mechanism to de-novo designed diastereomeric cell-selective antimicrobial peptides.
description
2001 nî lūn-bûn
@nan
2001 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
From "carpet" mechanism to de- ...... ective antimicrobial peptides.
@ast
From "carpet" mechanism to de- ...... ective antimicrobial peptides.
@en
From "carpet" mechanism to de- ...... ective antimicrobial peptides.
@nl
type
label
From "carpet" mechanism to de- ...... ective antimicrobial peptides.
@ast
From "carpet" mechanism to de- ...... ective antimicrobial peptides.
@en
From "carpet" mechanism to de- ...... ective antimicrobial peptides.
@nl
prefLabel
From "carpet" mechanism to de- ...... ective antimicrobial peptides.
@ast
From "carpet" mechanism to de- ...... ective antimicrobial peptides.
@en
From "carpet" mechanism to de- ...... ective antimicrobial peptides.
@nl
P1433
P1476
From "carpet" mechanism to de- ...... ective antimicrobial peptides.
@en
P304
P356
10.1016/S0196-9781(01)00498-3
P577
2001-10-01T00:00:00Z