PrP(106-126) does not interact with membranes under physiological conditions.
about
A Synthetic mirror image of kalata B1 reveals that cyclotide activity is independent of a protein receptorGene coevolution and regulation lock cyclic plant defence peptides to their targetsPhosphatidylethanolamine binding is a conserved feature of cyclotide-membrane interactions.Identification and characterization of a new family of cell-penetrating peptides: cyclic cell-penetrating peptides.Neurotoxic mutants of the prion protein induce spontaneous ionic currents in cultured cellsDecoding the membrane activity of the cyclotide kalata B1: the importance of phosphatidylethanolamine phospholipids and lipid organization on hemolytic and anti-HIV activitiesThe NALP3 inflammasome is involved in neurotoxic prion peptide-induced microglial activationDevelopment of a μO-Conotoxin Analogue with Improved Lipid Membrane Interactions and Potency for the Analgesic Sodium Channel NaV1.8.REST alleviates neurotoxic prion peptide-induced synaptic abnormalities, neurofibrillary degeneration and neuronal death partially via LRP6-mediated Wnt-β-catenin signaling.Characterization of cell-surface prion protein relative to its recombinant analogue: insights from molecular dynamics simulations of diglycosylated, membrane-bound human prion protein.Broad spectrum antiviral activity for paramyxoviruses is modulated by biophysical properties of fusion inhibitory peptides.Membrane Disruption Mechanism of a Prion Peptide (106-126) Investigated by Atomic Force Microscopy, Raman and Electron Paramagnetic Resonance Spectroscopy.C-Abl tyrosine kinase mediates neurotoxic prion peptide-induced neuronal apoptosis via regulating mitochondrial homeostasis.Unique structural properties associated with mouse prion Δ105-125 protein.Cyclization of the antimicrobial peptide gomesin with native chemical ligation: influences on stability and bioactivity.Interaction of Tarantula Venom Peptide ProTx-II with Lipid Membranes Is a Prerequisite for Its Inhibition of Human Voltage-gated Sodium Channel NaV1.7.Phospholipid composition of membranes directs prions down alternative aggregation pathways.Bacteria May Cope Differently from Similar Membrane Damage Caused by the Australian Tree Frog Antimicrobial Peptide Maculatin 1.1.Overexpression of BAT3 alleviates prion protein fragment PrP106-126-induced neuronal apoptosis.Interactions of the prion peptide (PrP 106-126) with brain capillary endothelial cells: coordinated cell killing and remodeling of intercellular junctions.Death Receptor 6 and Caspase-6 Regulate Prion Peptide-Induced Axonal Degeneration in Rat Spinal Neurons.Lysine to arginine mutagenesis of chlorotoxin enhances its cellular uptake.Mechanisms of bacterial membrane permeabilization by crotalicidin (Ctn) and its fragment Ctn(15-34), antimicrobial peptides from rattlesnake venom.Development of cell-penetrating peptide-based drug leads to inhibit MDMX:p53 and MDM2:p53 interactions.
P2860
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P2860
PrP(106-126) does not interact with membranes under physiological conditions.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
PrP(106-126) does not interact with membranes under physiological conditions.
@en
type
label
PrP(106-126) does not interact with membranes under physiological conditions.
@en
prefLabel
PrP(106-126) does not interact with membranes under physiological conditions.
@en
P2860
P50
P1433
P1476
PrP(106-126) does not interact with membranes under physiological conditions.
@en
P2093
Miguel A R B Castanho
P2860
P304
P356
10.1529/BIOPHYSJ.108.131458
P407
P577
2008-05-09T00:00:00Z