All Stories

  1. Processes and mechanisms underlying burst of giant unilamellar vesicles induced by antimicrobial peptides and compounds
  2. Effect of Phosphatidylethanolamine on Pore Formation Induced by the Antimicrobial Peptide PGLa
  3. Effect of membrane tension on antimicrobial peptide PGLa-induced pore formation in lipid bilayers
  4. Estimation of negative membrane tension in lipid bilayers and its effect on antimicrobial peptide magainin 2-induced pore formation
  5. Relationship between antimicrobial peptides-induced cell membrane damage and bactericidal activity
  6. Antimicrobial peptide magainin 2-induced rupture of single giant unilamellar vesicles comprising E. coli polar lipids
  7. Effect of monolayer spontaneous curvature on constant tension-induced pore formation in lipid bilayers
  8. Role of interfacial hydrophobicity in antimicrobial peptide magainin 2-induced nanopore formation
  9. Single-Cell Analysis of the Antimicrobial and Bactericidal Activities of the Antimicrobial Peptide Magainin 2
  10. Effect of osmotic pressure on pore formation in lipid bilayers by the antimicrobial peptide magainin 2
  11. Sulfur-doped carbon dots@polydopamine-functionalized magnetic silver nanocubes for dual-modality detection of norovirus
  12. A Single GUV Method for Revealing the Action of Cell-Penetrating Peptides in Biomembranes
  13. Translocation and entry of label-free AMP, PGLa, without pore formation
  14. Membrane potential enhances the entry of a short AMP into bacterial cells and lipid vesicles
  15. Fluorescent and electrochemical dual-mode detection of Chikungunya virus E1 protein using fluorophore-embedded and redox probe-encapsulated liposomes
  16. Effect of membrane potential on pore formation by the antimicrobial peptide magainin 2 in lipid bilayers
  17. Estimation of membrane tension in a GUV in a buffer containing a physiological conc. of ions
  18. Use of Target-Specific Liposome and Magnetic Nanoparticle Conjugation for the Amplified Detection of Norovirus
  19. Development of a new method to detect the entry of label-free peptides into vesicle lumen
  20. Effect of membrane potential on activities of AMPs and CPPs revealed by the single GUV method
  21. Membrane potential enhances the rate of entry of cell-penetrating peptides (CPPs) into the GUV lumen
  22. Membrane potential enhances membrane damage induced by antimicrobial peptide lactoferricin B
  23. The role of membrane tension in the action of antimicrobial peptides and cell-penetrating peptides in biomembranes
  24. Asymmetric distribution of lipids and peptides induces asymmetric lipid packing and membrane tension
  25. Elementary Processes and Mechanisms of Interactions of Antimicrobial Peptides with Membranes—Single Giant Unilamellar Vesicle Studies—
  26. Elementary processes of antimicrobial peptide PGLa-induced pore formation in lipid bilayers
  27. Membrane tension enhances the rate of transbilayer diffusion of lipid molecules
  28. Continuous detection of entry of cell-penetrating peptide transportan 10 into single vesicles
  29. Elementary processes for the entry of cell-penetrating peptides into lipid bilayer vesicles and bacterial cells
  30. Mechanism of Initial Stage of Pore Formation Induced by Antimicrobial Peptide Magainin 2
  31. Low-pH-Induced Lamellar to Bicontinuous Primitive Cubic Phase Transition in Dioleoylphosphatidylserine/Monoolein Membranes
  32. Entry of a Six-Residue Antimicrobial Peptide Derived from Lactoferricin B into Single Vesicles and Escherichia coli Cells without Damaging their Membranes
  33. Experimental Estimation of Membrane Tension Induced by Osmotic Pressure
  34. Effects of Mechanical Properties of Lipid Bilayers on the Entry of Cell-Penetrating Peptides into Single Vesicles
  35. Effects of Lipid Compositions on the Entry of Cell Penetrating Peptide Oligoarginine into Single Vesicles
  36. Experimental Estimation of Membrane Tension Induced by Osmotic Pressure
  37. Effects of Lipid Composition on the Entry of Cell-Penetrating Peptide Oligoarginine into Single Vesicles
  38. Activation Energy of the Low-pH-Induced Lamellar to Bicontinuous Cubic Phase Transition in Dioleoylphosphatidylserine/Monoolein
  39. Analysis of constant tension-induced rupture of lipid membranes using activation energy
  40. Antimicrobial Peptide Lactoferricin B-Induced Rapid Leakage of Internal Contents from Single Giant Unilamellar Vesicles
  41. Communication: Activation energy of tension-induced pore formation in lipid membranes
  42. Electrostatic interaction effects on tension-induced pore formation in lipid membranes
  43. Stretch-Activated Pore of the Antimicrobial Peptide, Magainin 2
  44. Initial Step of pH-Jump-Induced Lamellar to Bicontinuous Cubic Phase Transition in Dioleoylphosphatidylserine/Monoolein
  45. A Model for Targeting Colon Carcinoma Cells Using Single-Chain Variable Fragments Anchored on Virus-Like Particles via Glycosyl Phosphatidylinositol Anchor
  46. Entry of Cell-Penetrating Peptide Transportan 10 into a Single Vesicle by Translocating Across Lipid Membrane and Its Induced Pores
  47. The single GUV method for revealing the functions of antimicrobial, pore-forming toxin, and cell-penetrating peptides or proteins
  48. Rate Constant of Tension-Induced Pore Formation in Lipid Membranes
  49. The Single-Giant Unilamellar Vesicle Method Reveals Lysenin-Induced Pore Formation in Lipid Membranes Containing Sphingomyelin
  50. A membrane filtering method for the purification of giant unilamellar vesicles
  51. Kinetics of low pH-induced lamellar to bicontinuous cubic phase transition in dioleoylphosphatidylserine/monoolein
  52. Spontaneous insertion of lipopolysaccharide into lipid membranes from aqueous solution
  53. Kinetic Pathway of Antimicrobial Peptide Magainin 2-Induced Pore Formation in Lipid Membranes
  54. 単一GUV法による抗菌ペプチドのポア形成の研究
  55. The size of the pore in lipid membranes induced by antimicrobial peptide magainin 2
  56. Magainin 2-Induced Pore Formation in the Lipid Membranes Depends on Its Concentration in the Membrane Interface
  57. Chapter 7 Transformation Between Liposomes and Cubic Phases of Biological Lipid Membranes Induced by Modulation of Electrostatic Interactions
  58. Water permeability of lipid membranes of GUVs and its dependence on actin cytoskeletons inside the GUVs
  59. High affinity Zn2+ inhibitory site(s) for the trypsin-like peptidase of the 20S proteasome
  60. Low-pH-Induced Transformation of Bilayer Membrane into Bicontinuous Cubic Phase in Dioleoylphosphatidylserine/Monoolein Membranes
  61. Chapter 5 The Single Guv Method to Reveal Elementary Processes of Leakage of Internal Contents from Liposomes Induced by Antimicrobial Substances
  62. Effects of Surface Charge Density of Lipid Membranes on the Pore Formation Induced by Magainin 2
  63. Single GUV Method Reveals Interaction of Tea Catechin (−)-Epigallocatechin Gallate with Lipid Membranes
  64. Vesicle Fission of Giant Unilamellar Vesicles of Liquid-Ordered-Phase Membranes Induced by Amphiphiles with a Single Long Hydrocarbon Chain
  65. The “Le Chatelier's Principle”-Governed Response of Actin Filaments to Osmotic Stress
  66. Single Giant Unilamellar Vesicle Method Reveals Effect of Antimicrobial Peptide, Magainin 2, and Antibacterial Substance, Tea Catechin, on Membrane Permeability and Membrane Structure
  67. Single Giant Unilamellar Vesicle Method Reveals Effect of Antimicrobial Peptide Magainin 2 on Membrane Permeability
  68. Formation of Cubic Phases from Large Unilamellar Vesicles of Dioleoylphosphatidylglycerol/Monoolein Membranes Induced by Low Concentrations of Ca2+
  69. The effect of peptides and ions interacting with an electrically neutral membrane interface on the structure and stability of lipid membranes in the liquid-crystalline phase and in the liquid-ordered phase
  70. Cationic DMPC/DMTAP Lipid Bilayers:  Local Lateral Polarization of Phosphatidylcholine Headgroups
  71. Effect of Positively Charged Short Peptides on Stability of Cubic Phases of Monoolein/Dioleoylphosphatidic Acid Mixtures
  72. Design and Facile Synthesis of Neoglycolipids as Lactosylceramide Mimetics and Their Transformation into Glycoliposomes
  73. The Single GUV Method for Probing Biomembrane Structure and Function
  74. Stability of giant unilamellar vesicles and large unilamellar vesicles of liquid-ordered phase membranes in the presence of Triton X-100
  75. Shape Changes and Vesicle Fission of Giant Unilamellar Vesicles of Liquid-Ordered Phase Membrane Induced by Lysophosphatidylcholine
  76. Lipid Membrane Formation by Vesicle Fusion on Silicon Dioxide Surfaces Modified with Alkyl Self-Assembled Monolayer Islands
  77. Optical nanospectroscopy applications in material science
  78. Membrane Fusion of Giant Unilamellar Vesicles of Neutral Phospholipid Membranes Induced by La3+
  79. Low concentration of dioleoylphosphatidic acid induces an inverted hexagonal (HII) phase transition in dipalmitoleoylphosphatidylethanolamine membranes
  80. Low pH Stabilizes the Inverted Hexagonal II Phase in Dipalmitoleoylphosphatidylethanolamine Membrane
  81. Atomic force microscopy studies of interaction of the 20S proteasome with supported lipid bilayers
  82. Effect of de Novo Designed Peptides Interacting with the Lipid-Membrane Interface on the Stability of the Cubic Phases of the Monoolein Membrane
  83. Mechanical response of single filamin A (ABP-280) molecules and its role in the actin cytoskeleton
  84. Shape Changes of Giant Unilamellar Vesicles of Phosphatidylcholine Induced by a De Novo Designed Peptide Interacting with Their Membrane Interface
  85. La3+ and Gd3+ induce shape change of giant unilamellar vesicles of phosphatidylcholine
  86. A model of pressure-induced interdigitation of phospholipid membranes
  87. A new method for the preparation of giant liposomes in high salt concentrations and growth of protein microcrystals in them
  88. La3+ stabilizes the hexagonal II (HII) phase in phosphatidylethanolamine membranes
  89. Effect of Electrostatic Interactions on Phase Stability of Cubic Phases of Membranes of Monoolein/Dioleoylphosphatidic Acid Mixtures
  90. The mechanism of the stabilization of the hexagonal II (H II ) phase in phosphatidylethanolamine membranes in the presence of low concentrations of dimethyl sulfoxide
  91. Mechanical unfolding of single filamin A (ABP‐280) molecules detected by atomic force microscopy
  92. Low concentration of DMSO stabilizes the bilayer gel phase rather than the interdigitated gel phase in dihexadecylphosphatidylcholine membrane
  93. Effects of electrostatic interaction on the phase stability and structures of cubic phases of monoolein/oleic acid mixture membranes
  94. Effects of solvents interacting favorably with hydrophilic segments of the membrane surface of phosphatidylcholine on their gel-phase membranes in water
  95. Low pH Induces an Interdigitated Gel to Bilayer Gel Phase Transition in Dihexadecylphosphatidylcholine Membrane
  96. Intermembrane distance in multilamellar vesicles of phosphatidylcholine depends on the interaction free energy between solvents and the hydrophilic segments of the membrane surface
  97. Ion Permeability of a Membrane with Soft Polar Interfaces. 2. The Polar Zones as the Rate-Determining Step
  98. Phase transition between hexagonal II(HII) and liquid-crystalline phase induced by interaction between solvents and segments of the membrane surface of dioleoylphosphatidylethanolamine
  99. Osmotic stress induces a phase transition from interdigitated gel phase to bilayer gel phase in multilamellar vesicles of dihexadecylphosphatidylcholine
  100. Interaction of the surface of biomembrane with solvents: structure of multilamellar vesicles of dipalmitoylphosphatidylcholine in acetone-water mixtures
  101. Organic solvents induce interdigitated gel structures in multilamellar vesicles of dipalmitoylphosphatidylcholine
  102. Polymorphism of F-Actin Assembly. 1. A Quantitative Phase Diagram of F-Actin
  103. Formation of ion channels in lipid bilayers by a peptide with the predicted transmembrane sequence of botulinum neurotoxin A
  104. Direct evidence of induction of interdigitated gel structure in large unilamellar vesicles of dipalmitoylphosphatidylcholine by ethanol: studies by excimer method and high-resolution electron cryomicroscopy
  105. Effect of oligomers of ethylene glycol on thermotropic phase transition of dipalmitoylphosphatidylcholine multilamellar vesicles
  106. Phase transitions of phospholipid vesicles under osmotic stress and in the presence of ethylene glycol
  107. Studies of alcohol-induced interdigitated gel phase in phosphatidylcholine multilamellar vesicles by the excimer method
  108. Phase separation of triton X-100 micelle solution induced by osmotic stress
  109. Deformation and instability of membrane structure of phospholipid vesicles caused by osmophobic association: mechanical stress model for the mechanism of poly(ethylene glycol)-induced membrane fusion
  110. Poly(ethylene glycol)-induced shrinkage of Sephadex gel. A model system for quantitative analysis of osmoelastic coupling
  111. Osmoelastic coupling in biological structures: formation of parallel bundles of actin filaments in a crystalline-like structure caused by osmotic stress
  112. Osmoelastic coupling in biological structures: a comprehensive thermodynamic analysis of the osmotic response of phospholipid vesicles and a reevaluation of the "dehydration force" theory
  113. Osmoelastic coupling in biological structures: decrease in membrane fluidity and osmophobic association of phospholipid vesicles in response to osmotic stress
  114. Phase Transition in Di-oleoylphosphatidylglycerol/Monoolein Membranes due to Interactions of Positively Charged Peptides at their Lipid Membrane-Interface