High-throughput discovery of broad-spectrum peptide antibiotics.
about
A peptide derived from phage display library exhibits antibacterial activity against E. coli and Pseudomonas aeruginosaFrom design to screening: a new antimicrobial peptide discovery pipelineBead diffusion assay for discovering antimicrobial cyclic peptides.Describing the mechanism of antimicrobial peptide action with the interfacial activity modelGain-of-function analogues of the pore-forming peptide melittin selected by orthogonal high-throughput screening.Host Cell Interactions Are a Significant Barrier to the Clinical Utility of Peptide Antibiotics.A thermodynamic approach to the mechanism of cell-penetrating peptides in model membranesSynthetic molecular evolution of pore-forming peptides by iterative combinatorial library screening.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.Examination of bacterial inhibition using a catalytic DNAExploring the pharmacological potential of promiscuous host-defense peptides: from natural screenings to biotechnological applications.Determining the mechanism of membrane permeabilizing peptides: identification of potent, equilibrium pore-formersHemolytic activity of membrane-active peptides correlates with the thermodynamics of binding to 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine bilayersComparative Analysis of the Antimicrobial Activities of Plant Defensin-Like and Ultrashort Peptides against Food-Spoiling BacteriaDirect cytosolic delivery of polar cargo to cells by spontaneous membrane-translocating peptides.Antimicrobial peptides: successes, challenges and unanswered questions.Membrane-active host defense peptides--challenges and perspectives for the development of novel anticancer drugs.Advances in the arsenal of tools available enabling the discovery of novel lantibiotics with therapeutic potential.Spontaneous membrane-translocating peptides by orthogonal high-throughput screening.A lack of synergy between membrane-permeabilizing cationic antimicrobial peptides and conventional antibiotics.Pituitary adenylate cyclase-activating polypeptide is a potent broad-spectrum antimicrobial peptide: Structure-activity relationships.Synthetic molecular evolution of hybrid cell penetrating peptides.
P2860
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P2860
High-throughput discovery of broad-spectrum peptide antibiotics.
description
2010 nî lūn-bûn
@nan
2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
High-throughput discovery of broad-spectrum peptide antibiotics.
@ast
High-throughput discovery of broad-spectrum peptide antibiotics.
@en
High-throughput discovery of broad-spectrum peptide antibiotics.
@nl
type
label
High-throughput discovery of broad-spectrum peptide antibiotics.
@ast
High-throughput discovery of broad-spectrum peptide antibiotics.
@en
High-throughput discovery of broad-spectrum peptide antibiotics.
@nl
prefLabel
High-throughput discovery of broad-spectrum peptide antibiotics.
@ast
High-throughput discovery of broad-spectrum peptide antibiotics.
@en
High-throughput discovery of broad-spectrum peptide antibiotics.
@nl
P2860
P356
P1433
P1476
High-throughput discovery of broad-spectrum peptide antibiotics.
@en
P2093
Ramesh Rathinakumar
William C Wimley
P2860
P304
P356
10.1096/FJ.10-157040
P407
P577
2010-04-21T00:00:00Z