scholarly article | Q13442814 |
P356 | DOI | 10.1021/BI980539Y |
P698 | PubMed publication ID | 9718308 |
P50 | author | Richard M. Epand | Q43656907 |
P2093 | author name string | Ishibe N | |
Matsuzaki K | |||
Nakata S | |||
Miyajima K | |||
Sugishita K | |||
Ueha M | |||
P433 | issue | 34 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 11856-11863 | |
P577 | publication date | 1998-08-01 | |
P1433 | published in | Biochemistry | Q764876 |
P1476 | title | Relationship of membrane curvature to the formation of pores by magainin 2 | |
P478 | volume | 37 |
Q90302756 | A coarse-grained approach to studying the interactions of the antimicrobial peptides aurein 1.2 and maculatin 1.1 with POPG/POPE lipid mixtures |
Q37034573 | A common landscape for membrane-active peptides |
Q36899418 | A critical evaluation of random copolymer mimesis of homogeneous antimicrobial peptides |
Q35089446 | Amyloid beta-protein interactions with membranes and cholesterol: causes or casualties of Alzheimer's disease |
Q58440961 | Analogs of the antimicrobial peptide trichogin having opposite membrane properties |
Q86886447 | Analysis of the flexibility and stability of the structure of magainin in a bilayer, and in aqueous and nonaqueous solutions using molecular dynamics simulations |
Q38701785 | Antibacterial Peptides: Opportunities for the Prevention and Treatment of Dental Caries. |
Q47723258 | Antimicrobial Peptides: Diversity, Mechanism of Action and Strategies to Improve the Activity and Biocompatibility In Vivo |
Q42074628 | Antimicrobial activity and membrane selective interactions of a synthetic lipopeptide MSI-843 |
Q38941806 | Antimicrobial peptide GW-H1-induced apoptosis of human gastric cancer AGS cell line is enhanced by suppression of autophagy |
Q37724182 | Antimicrobial peptides and induced membrane curvature: geometry, coordination chemistry, and molecular engineering |
Q38222114 | Antimicrobial peptides from scorpion venoms |
Q33536544 | Antimicrobial peptides in mammalian and insect host defence |
Q37918722 | Antimicrobial peptides: modes of mechanism, modulation of defense responses |
Q29547675 | Antimicrobial peptides: pore formers or metabolic inhibitors in bacteria? |
Q35087061 | Bicelles in structure-function studies of membrane-associated proteins |
Q43980980 | Binding of the antimicrobial peptide temporin L to liposomes assessed by Trp fluorescence |
Q94526373 | Bioactive Peptides: Synthesis, Properties, and Applications in the Packaging and Preservation of Food |
Q34112765 | Biophysical investigations of membrane perturbations by polypeptides using solid-state NMR spectroscopy (review). |
Q35751443 | Calorimetric, x-ray diffraction, and spectroscopic studies of the thermotropic phase behavior and organization of tetramyristoyl cardiolipin membranes |
Q37727568 | Cardiolipin prevents membrane translocation and permeabilization by daptomycin. |
Q60419791 | Chapter Five Liposome-Based Biomembrane Mimetic Systems: Implications for Lipid–Peptide Interactions |
Q42013282 | Cholesterol reduces pardaxin's dynamics-a barrel-stave mechanism of membrane disruption investigated by solid-state NMR. |
Q42085842 | Coarse-grained simulation studies of peptide-induced pore formation. |
Q36781952 | Common mechanism unites membrane poration by amyloid and antimicrobial peptides |
Q40110502 | Comparing the action of HT61 and chlorhexidine on natural and model Staphylococcus aureus membranes. |
Q28362033 | Comparison of the membrane association of two antimicrobial peptides, magainin 2 and indolicidin |
Q39793865 | Conformation of a bactericidal domain of puroindoline a: structure and mechanism of action of a 13-residue antimicrobial peptide |
Q34182358 | Conformation, orientation, and adsorption kinetics of dermaseptin B2 onto synthetic supports at aqueous/solid interface |
Q36338409 | Correlating antimicrobial activity and model membrane leakage induced by nylon-3 polymers and detergents |
Q60920350 | Could Cardiolipin Protect Membranes against the Action of Certain Antimicrobial Peptides? Aurein 1.2, a Case Study |
Q41897132 | Criterion for amino acid composition of defensins and antimicrobial peptides based on geometry of membrane destabilization |
Q33967505 | Crystallization and preliminary X-ray analysis of cecropin B from Bombyx mori |
Q92519594 | De Novo Design and In Vitro Testing of Antimicrobial Peptides against Gram-Negative Bacteria |
Q50029734 | Dermaseptins as potential antirabies compounds |
Q47753580 | Differential Interaction of Antimicrobial Peptides with Lipid Structures Studied by Coarse-Grained Molecular Dynamics Simulations |
Q33789733 | Differential scanning calorimetry and X-ray diffraction studies of the specificity of the interaction of antimicrobial peptides with membrane-mimetic systems |
Q40900833 | Diffusion as a probe of the heterogeneity of antimicrobial peptide-membrane interactions |
Q33789705 | Diversity of antimicrobial peptides and their mechanisms of action |
Q90296142 | Effect of helical kink in antimicrobial peptides on membrane pore formation |
Q73614145 | Effect of magainin, class L, and class A amphipathic peptides on fatty acid spin labels in lipid bilayers |
Q28365530 | Effects of histatin 5 and derived peptides on Candida albicans |
Q42805350 | Effects of the hinge region of cecropin A(1-8)-magainin 2(1-12), a synthetic antimicrobial peptide, on liposomes, bacterial and tumor cells |
Q43104545 | Enhanced activity of cyclic transporter sequences driven by phase behavior of peptide-lipid complexes |
Q27680196 | Evidence for Phenylalanine Zipper-Mediated Dimerization in the X-ray Crystal Structure of a Magainin 2 Analogue |
Q37282305 | Free energies of molecular bound states in lipid bilayers: lethal concentrations of antimicrobial peptides |
Q42143437 | Förster resonance energy transfer (FRET) between heterogeneously distributed probes: application to lipid nanodomains and pores |
Q36238251 | Helical antimicrobial polypeptides with radial amphiphilicity |
Q33925341 | Identification of a novel lytic peptide for the treatment of solid tumours. |
Q31008813 | Induction of morphological changes in model lipid membranes and the mechanism of membrane disruption by a large scorpion-derived pore-forming peptide. |
Q42621867 | Influence of lipid composition on membrane activity of antimicrobial phenylene ethynylene oligomers |
Q37724175 | Influenza virus A M2 protein generates negative Gaussian membrane curvature necessary for budding and scission. |
Q37331938 | Interaction between a cationic surfactant-like peptide and lipid vesicles and its relationship to antimicrobial activity |
Q38630326 | Interaction of LL-37 with model membrane systems of different complexity: influence of the lipid matrix |
Q33789711 | Interaction of antimicrobial peptides with biological and model membranes: structural and charge requirements for activity |
Q77781027 | Interactions of an antimicrobial peptide, magainin 2, with lipopolysaccharide-containing liposomes as a model for outer membranes of gram-negative bacteria |
Q42406521 | Interactions of cationic-hydrophobic peptides with lipid bilayers: a Monte Carlo simulation method |
Q37349937 | Interactions of surfactants with lipid membranes |
Q50562558 | Kinetic Pathway of Antimicrobial Peptide Magainin 2-Induced Pore Formation in Lipid Membranes |
Q41762155 | Lacticin Q-mediated selective toxicity depending on physicochemical features of membrane components |
Q54376790 | Lipid Composition Influences the Membrane-Disrupting Activity of Antimicrobial Methacrylate Co-polymers |
Q37227423 | Lipid composition-dependent membrane fragmentation and pore-forming mechanisms of membrane disruption by pexiganan (MSI-78) |
Q42194327 | Lipid interactions of LAH4, a peptide with antimicrobial and nucleic acid transfection activities |
Q77521412 | Lipid polymorphism and protein-lipid interactions |
Q24537642 | MSI-78, an Analogue of the Magainin Antimicrobial Peptides, Disrupts Lipid Bilayer Structure via Positive Curvature Strain |
Q30484999 | Magainin 2 in action: distinct modes of membrane permeabilization in living bacterial and mammalian cells |
Q37260254 | Magainin 2 revisited: a test of the quantitative model for the all-or-none permeabilization of phospholipid vesicles |
Q77521430 | Magainins as paradigm for the mode of action of pore forming polypeptides |
Q34352457 | Many-body effect of antimicrobial peptides: on the correlation between lipid's spontaneous curvature and pore formation |
Q37473662 | Mapping membrane activity in undiscovered peptide sequence space using machine learning. |
Q37081714 | Mechanism of a prototypical synthetic membrane-active antimicrobial: Efficient hole-punching via interaction with negative intrinsic curvature lipids. |
Q33789716 | Mechanism of the binding, insertion and destabilization of phospholipid bilayer membranes by alpha-helical antimicrobial and cell non-selective membrane-lytic peptides |
Q92538088 | Mechanisms of Action for Antimicrobial Peptides With Antibacterial and Antibiofilm Functions |
Q41921581 | Mechanisms of alpha-defensin bactericidal action: comparative membrane disruption by Cryptdin-4 and its disulfide-null analogue |
Q34189385 | Melittin-induced bilayer leakage depends on lipid material properties: evidence for toroidal pores |
Q41867473 | Melittin-lipid bilayer interactions and the role of cholesterol |
Q58717273 | Membrane Active Peptides and Their Biophysical Characterization |
Q90523356 | Membrane Remodeling by the Lytic Fragment of SticholysinII: Implications for the Toroidal Pore Model |
Q90708918 | Membrane activity of two short Trp-rich amphipathic peptides |
Q34139541 | Membrane composition determines pardaxin's mechanism of lipid bilayer disruption |
Q35269863 | Membrane interaction of antimicrobial peptides using E. coli lipid extract as model bacterial cell membranes and SFG spectroscopy |
Q40285596 | Membrane remodeling by the M2 amphipathic helix drives influenza virus membrane scission. |
Q35556337 | Membrane-proximal external HIV-1 gp41 motif adapted for destabilizing the highly rigid viral envelope |
Q54426552 | Minimum requirements of hydrophobic and hydrophilic features in cationic peptide antibiotics (CPAs): pharmacophore generation and validation with cationic steroid antibiotics (CSAs). |
Q53928061 | Molecular basis for membrane selectivity of NK-2, a potent peptide antibiotic derived from NK-lysin. |
Q33677435 | Molecular basis for nanoscopic membrane curvature generation from quantum mechanical models and synthetic transporter sequences |
Q38531326 | More Than a Pore: The Interplay of Pore-Forming Proteins and Lipid Membranes. |
Q33552978 | NMR structure of a viral peptide inserted in artificial membranes: a view on the early steps of the birnavirus entry process |
Q34180605 | New cationic lipids form channel-like pores in phospholipid bilayers |
Q35600198 | Oncolytic activities of host defense peptides |
Q74127743 | Optical characterization of liposomes by right angle light scattering and turbidity measurement |
Q34174800 | Orientation and effects of mastoparan X on phospholipid bicelles |
Q40299393 | Orientation and pore-forming mechanism of a scorpion pore-forming peptide bound to magnetically oriented lipid bilayers |
Q24563255 | PB1-F2, an influenza A virus-encoded proapoptotic mitochondrial protein, creates variably sized pores in planar lipid membranes |
Q35121277 | Paradoxical lipid dependence of pores formed by the Escherichia coli alpha-hemolysin in planar phospholipid bilayer membranes |
Q81197969 | Perturbation of a lipid membrane by amphipathic peptides and its role in pore formation |
Q89743571 | Phase Diagram for a Lysyl-Phosphatidylglycerol Analogue in Biomimetic Mixed Monolayers with Phosphatidylglycerol: Insights into the Tunable Properties of Bacterial Membranes |
Q24676276 | Phosphatidylethanolamine critically supports internalization of cell-penetrating protein C inhibitor |
Q36299680 | Phosphatidylethanolamine enhances amyloid fiber-dependent membrane fragmentation. |
Q40172265 | Polar angle as a determinant of amphipathic alpha-helix-lipid interactions: a model peptide study |
Q44565961 | Pore formation by equinatoxin II, a eukaryotic protein toxin, occurs by induction of nonlamellar lipid structures |
Q30388868 | Pro-apoptotic Bax molecules densely populate the edges of membrane pores |
Q47111286 | Protein Structure Insights into the Bilayer Interactions of the Saposin-Like Domain of Solanum tuberosum Aspartic Protease |
Q104584577 | Rational Design of Helix-Stabilized Antimicrobial Peptide Foldamers Containing α,α-Disubstituted Amino Acids or Side-Chain Stapling |
Q30581778 | Real-time measurement of membrane conformational states induced by antimicrobial peptides: balance between recovery and lysis |
Q61799995 | Reassessing the Host Defense Peptide Landscape |
Q34531269 | SV40 late protein VP4 forms toroidal pores to disrupt membranes for viral release |
Q44394283 | Selective cytotoxicity following Arg-to-Lys substitution in tritrpticin adopting a unique amphipathic turn structure |
Q46642618 | Selectivity in the mechanism of action of antimicrobial mastoparan peptide Polybia-MP1. |
Q42092818 | Small changes in the primary structure of transportan 10 alter the thermodynamics and kinetics of its interaction with phospholipid vesicles |
Q34680351 | Solid-state NMR investigation of the membrane-disrupting mechanism of antimicrobial peptides MSI-78 and MSI-594 derived from magainin 2 and melittin |
Q42173802 | Solution structure and interaction of the antimicrobial polyphemusins with lipid membranes |
Q33789720 | Structural features of helical antimicrobial peptides: their potential to modulate activity on model membranes and biological cells |
Q27654130 | Structure and Membrane Interactions of the Antibiotic Peptide Dermadistinctin K by Multidimensional Solution and Oriented 15N and 31P Solid-State NMR Spectroscopy |
Q30157467 | Structure of transmembrane pore induced by Bax-derived peptide: evidence for lipidic pores. |
Q37325942 | Structure, membrane orientation, mechanism, and function of pexiganan--a highly potent antimicrobial peptide designed from magainin. |
Q54204440 | Synergism of Antimicrobial Frog Peptides Couples to Membrane Intrinsic Curvature Strain. |
Q33954399 | The SV40 late protein VP4 is a viroporin that forms pores to disrupt membranes for viral release |
Q35826297 | The Simian virus 40 late viral protein VP4 disrupts the nuclear envelope for viral release |
Q36957307 | The activity of the amphipathic peptide delta-lysin correlates with phospholipid acyl chain structure and bilayer elastic properties |
Q34757081 | The effect of membrane curvature on the conformation of antimicrobial peptides: implications for binding and the mechanism of action |
Q33789751 | The lantibiotic nisin, a special case or not? |
Q50562072 | The role of aromatic side-chains in amyloid growth and membrane interaction of the islet amyloid polypeptide fragment LANFLVH. |
Q64947425 | The role of membrane tension in the action of antimicrobial peptides and cell-penetrating peptides in biomembranes. |
Q37361213 | The roles of antimicrobial peptides in innate host defense |
Q74664871 | The structure of the antimicrobial active center of lactoferricin B bound to sodium dodecyl sulfate micelles |
Q33789739 | The structure, dynamics and orientation of antimicrobial peptides in membranes by multidimensional solid-state NMR spectroscopy |
Q41770407 | The use of antimicrobial peptides in ophthalmology: an experimental study in corneal preservation and the management of bacterial keratitis |
Q90139600 | Toward building a physical model for membrane selectivity of antimicrobial peptides: making a quantitative sense of the selectivity |
Q35790869 | Towards understanding the Tat translocation mechanism through structural and biophysical studies of the amphipathic region of TatA from Escherichia coli. |
Q35345277 | Translocation of HIV TAT peptide and analogues induced by multiplexed membrane and cytoskeletal interactions |
Q35512980 | Two interdependent mechanisms of antimicrobial activity allow for efficient killing in nylon-3-based polymeric mimics of innate immunity peptides |
Q24537440 | Voltage-induced nonconductive pre-pores and metastable single pores in unmodified planar lipid bilayer |
Q37414151 | Wasp mastoparans follow the same mechanism as the cell-penetrating peptide transportan 10. |
Q62659987 | What Can Pleiotropic Proteins in Innate Immunity Teach Us about Bioconjugation and Molecular Design? |
Q33789700 | Why and how are peptide-lipid interactions utilized for self-defense? Magainins and tachyplesins as archetypes |
Q52541184 | X-ray studies on the interaction of the antimicrobial peptide gramicidin S with microbial lipid extracts: evidence for cubic phase formation. |
Q44693554 | tBid forms a pore in the liposome membrane |
Search more.