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一种从β-淀粉样蛋白(Aβ)设计而来的短的无细胞毒性抗菌肽呈现出纳米结构并在体内显示出抗内毒素活性。

A short non-cytotoxic antimicrobial peptide designed from Aβ adopts a nanostructure and shows in vivo anti-endotoxin activity.

作者信息

Harioudh Munesh Kumar, Sahai Rohit, Mitra Kalyan, Ghosh Jimut Kanti

机构信息

Molecular and Structural Biology Division, CSIR-Central Drug Research Institute, Lucknow-226031, Uttar Pradesh, India.

出版信息

Chem Commun (Camb). 2017 Dec 5;53(97):13079-13082. doi: 10.1039/c7cc07547b.

DOI:10.1039/c7cc07547b
PMID:29168511
Abstract

Aβ residues with tryptophan in place of the lone methionine residue and three arginine residues added to its C-terminus exhibited augmented antibacterial activities and protected mice against a lethal dose of LPS. The results show the conversion of a Aβ segment into a cell-selective antimicrobial/anti-endotoxin peptide with nanostructure and cation-π interaction.

摘要

用色氨酸取代单个甲硫氨酸残基并在其C末端添加三个精氨酸残基的Aβ残基表现出增强的抗菌活性,并保护小鼠免受致死剂量的脂多糖侵害。结果表明,一个Aβ片段转化为具有纳米结构和阳离子-π相互作用的细胞选择性抗菌/抗内毒素肽。

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