Equinatoxin II permeabilizing activity depends on the presence of sphingomyelin and lipid phase coexistence
about
Cytochrome c causes pore formation in cardiolipin-containing membranesPlasmodium falciparum antigen 332 is a resident peripheral membrane protein of Maurer's cleftsStructural basis for self-assembly of a cytolytic pore lined by protein and lipidImaging the lipid-phase-dependent pore formation of equinatoxin II in droplet interface bilayers.Characterization of the Lipid-Binding Site of Equinatoxin II by NMR and Molecular Dynamics SimulationObserving the confinement potential of bacterial pore-forming toxin receptors inside rafts with nonblinking Eu(3+)-doped oxide nanoparticlesPE and PS Lipids Synergistically Enhance Membrane Poration by a Peptide with Anticancer PropertiesSynthetic biology of minimal systems.Nature's lessons in design: nanomachines to scaffold, remodel and shape membrane compartments.More Than a Pore: The Interplay of Pore-Forming Proteins and Lipid Membranes.Effects of HIV-1 gp41-Derived Virucidal Peptides on Virus-like Lipid Membranes.Oligomerization and pore formation by equinatoxin II inhibit endocytosis and lead to plasma membrane reorganization.A pore-forming toxin requires a specific residue for its activity in membranes with particular physicochemical properties.Automated analysis of giant unilamellar vesicles using circular Hough transformation.All-or-none versus graded: single-vesicle analysis reveals lipid composition effects on membrane permeabilization.The effect of cholesterol on the long-range network of interactions established among sea anemone Sticholysin II residues at the water-membrane interfacePores formed by Baxα5 relax to a smaller size and keep at equilibriumPurification and characterization of gigantoxin-4, a new actinoporin from the sea anemone Stichodactyla gigantea.Mechanistic differences in the membrane activity of Bax and Bcl-xL correlate with their opposing roles in apoptosis.Crystallization and preliminary crystallographic analysis of fragaceatoxin C, a pore-forming toxin from the sea anemone Actinia fragacea.Membrane promotes tBID interaction with BCL(XL).Confocal microscopy of giant vesicles supports the absence of HIV-1 neutralizing 2F5 antibody reactivity to plasma membrane phospholipids.Biophysical and biochemical strategies to understand membrane binding and pore formation by sticholysins, pore-forming proteins from a sea anemone.Alpha-Helical Fragaceatoxin C Nanopore Engineered for Double-Stranded and Single-Stranded Nucleic Acid Analysis.Subcellular localization of sphingomyelin revealed by two toxin-based probes in mammalian cells.Haemolytic actinoporins interact with carbohydrates using their lipid-binding module.Advances in structure determination by cryo-EM to unravel membrane-spanning pore formation
P2860
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P2860
Equinatoxin II permeabilizing activity depends on the presence of sphingomyelin and lipid phase coexistence
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Equinatoxin II permeabilizing ...... in and lipid phase coexistence
@en
Equinatoxin II permeabilizing ...... n and lipid phase coexistence.
@nl
type
label
Equinatoxin II permeabilizing ...... in and lipid phase coexistence
@en
Equinatoxin II permeabilizing ...... n and lipid phase coexistence.
@nl
prefLabel
Equinatoxin II permeabilizing ...... in and lipid phase coexistence
@en
Equinatoxin II permeabilizing ...... n and lipid phase coexistence.
@nl
P2093
P2860
P1433
P1476
Equinatoxin II permeabilizing ...... in and lipid phase coexistence
@en
P2093
Ana J García-Sáez
Kirsten Bacia
Peter Schön
Petra Malovrh
P2860
P304
P356
10.1529/BIOPHYSJ.108.129981
P407
P577
2008-04-04T00:00:00Z