• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

卵黄高磷蛋白衍生肽Pt5e对临床多重耐药菌的抗菌活性及作用方式

Antibacterial activity and modes of action of phosvitin-derived peptide Pt5e against clinical multi-drug resistance bacteria.

作者信息

Li Zhijian, Wang Peng, Jiang Chengyan, Cui Pengfei, Zhang Shicui

机构信息

Laboratory for Evolution & Development, Institute of Evolution & Marine Biodiversity and Department of Marine Biology, Ocean University of China, Qingdao 266003, China.

Laboratory for Evolution & Development, Institute of Evolution & Marine Biodiversity and Department of Marine Biology, Ocean University of China, Qingdao 266003, China; College of Life Science and Technology, Hong He University, Mengzi, Yunnan 661100, China.

出版信息

Fish Shellfish Immunol. 2016 Nov;58:370-379. doi: 10.1016/j.fsi.2016.09.044. Epub 2016 Sep 22.

DOI:10.1016/j.fsi.2016.09.044
PMID:27666191
Abstract

Pt5e, a mutant peptide derived from the C-terminal 55 residues of zebrafish phosvitin, has been suggested to be a novel antibacterial peptide. However, if it is applicable to clinical MDR bacteria remains to be tested. In this study, high-purity Pt5e was first expressed and purified by fusion with cationic elastin-like polypeptide. Pt5e was then shown to be capable of effectively killing all the five clinical MDR bacteria tested. Pt5e kill the MDR bacteria at several levels, including inserting into the bacterial membranes, causing the membrane depolarization and permeabilization, and inducing the intracellular apoptosis/necrosis. All these data suggest that Pt5e is a promising therapeutic potential as an antibiotics against clinical MDR bacteria.

摘要

Pt5e是一种源自斑马鱼卵黄高磷蛋白C末端55个残基的突变肽,已被认为是一种新型抗菌肽。然而,它是否适用于临床多重耐药菌仍有待测试。在本研究中,首先通过与阳离子弹性蛋白样多肽融合表达并纯化了高纯度的Pt5e。然后发现Pt5e能够有效杀灭所测试的全部五种临床多重耐药菌。Pt5e在多个层面杀死多重耐药菌,包括插入细菌细胞膜、导致膜去极化和通透性增加,以及诱导细胞内凋亡/坏死。所有这些数据表明,Pt5e作为一种抗临床多重耐药菌的抗生素具有有前景的治疗潜力。

相似文献

1
Antibacterial activity and modes of action of phosvitin-derived peptide Pt5e against clinical multi-drug resistance bacteria.卵黄高磷蛋白衍生肽Pt5e对临床多重耐药菌的抗菌活性及作用方式
Fish Shellfish Immunol. 2016 Nov;58:370-379. doi: 10.1016/j.fsi.2016.09.044. Epub 2016 Sep 22.
2
Augmentation of the antibacterial activities of Pt5-derived antimicrobial peptides (AMPs) by amino acid substitutions: Design of novel AMPs against MDR bacteria.通过氨基酸取代增强源自 Pt5 的抗菌肽 (AMPs) 的抗菌活性:针对 MDR 细菌的新型 AMP 的设计。
Fish Shellfish Immunol. 2018 Jun;77:100-111. doi: 10.1016/j.fsi.2018.03.031. Epub 2018 Mar 19.
3
Lipopolysaccharide neutralization by a novel peptide derived from phosvitin.一种新型来源于卵黄高磷蛋白的肽对脂多糖的中和作用。
Int J Biochem Cell Biol. 2013 Nov;45(11):2622-31. doi: 10.1016/j.biocel.2013.09.002. Epub 2013 Sep 9.
4
Antimicrobial-immunomodulatory activities of zebrafish phosvitin-derived peptide Pt5.斑马鱼卵黄蛋白衍生肽 Pt5 的抗菌-免疫调节活性。
Peptides. 2012 Oct;37(2):309-13. doi: 10.1016/j.peptides.2012.07.014. Epub 2012 Jul 27.
5
[Evolution of susceptibility to antibiotics of Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa and Acinetobacter baumanii, in a University Hospital Center of Beirut between 2005 and 2009].[2005年至2009年期间,贝鲁特一家大学医院中心大肠杆菌、肺炎克雷伯菌、铜绿假单胞菌和鲍曼不动杆菌对抗生素敏感性的演变]
Pathol Biol (Paris). 2012 Jun;60(3):e15-20. doi: 10.1016/j.patbio.2011.03.011. Epub 2011 Jun 29.
6
Phosvitin plays a critical role in the immunity of zebrafish embryos via acting as a pattern recognition receptor and an antimicrobial effector.磷酸化卵黄蛋白在斑马鱼胚胎的免疫中发挥重要作用,作为一种模式识别受体和抗菌效应分子。
J Biol Chem. 2011 Jun 24;286(25):22653-64. doi: 10.1074/jbc.M111.247635. Epub 2011 Apr 29.
7
Insect Antimicrobial Peptide Complexes Prevent Resistance Development in Bacteria.昆虫抗菌肽复合物可防止细菌产生耐药性。
PLoS One. 2015 Jul 15;10(7):e0130788. doi: 10.1371/journal.pone.0130788. eCollection 2015.
8
Synergistic activity profile of an antimicrobial peptide against multidrug-resistant and extensively drug-resistant strains of Gram-negative bacterial pathogens.一种抗菌肽对革兰氏阴性细菌病原体的多重耐药和广泛耐药菌株的协同活性谱。
J Pept Sci. 2017 Apr;23(4):329-333. doi: 10.1002/psc.2978. Epub 2017 Feb 8.
9
Piscidin is highly active against carbapenem-resistant Acinetobacter baumannii and NDM-1-producing Klebsiella pneumonia in a systemic Septicaemia infection mouse model.在全身性败血症感染小鼠模型中,杀鱼菌素对耐碳青霉烯类鲍曼不动杆菌和产NDM-1的肺炎克雷伯菌具有高度活性。
Mar Drugs. 2015 Apr 14;13(4):2287-305. doi: 10.3390/md13042287.
10
Antimicrobial activities and membrane-active mechanism of CPF-C1 against multidrug-resistant bacteria, a novel antimicrobial peptide derived from skin secretions of the tetraploid frog Xenopus clivii.CPF-C1(一种源自四倍体青蛙克氏爪蟾皮肤分泌物的新型抗菌肽)对多重耐药菌的抗菌活性及膜作用机制
J Pept Sci. 2014 Nov;20(11):876-84. doi: 10.1002/psc.2679. Epub 2014 Aug 6.

引用本文的文献

1
Recent Advances in Marine-Derived Compounds as Potent Antibacterial and Antifungal Agents: A Comprehensive Review.海洋来源化合物作为强效抗菌和抗真菌剂的最新进展:全面综述。
Mar Drugs. 2024 Jul 29;22(8):348. doi: 10.3390/md22080348.
2
The antibacterial mechanism of phenylacetic acid isolated from L2 against .从 L2 中分离出的苯乙酸对 … 的抗菌机制。
PeerJ. 2022 Nov 8;10:e14304. doi: 10.7717/peerj.14304. eCollection 2022.
3
Improving the Activity of Antimicrobial Peptides Against Aquatic Pathogen Bacteria by Amino Acid Substitutions and Changing the Ratio of Hydrophobic Residues.
通过氨基酸取代和改变疏水残基比例提高抗菌肽对水生病原菌的活性
Front Microbiol. 2021 Oct 18;12:773076. doi: 10.3389/fmicb.2021.773076. eCollection 2021.
4
Chemical composition, antibacterial activity and action mechanism of different extracts from hawthorn (Crataegus pinnatifida Bge.).山楂(Crataegus pinnatifida Bge.)不同提取物的化学成分、抗菌活性及作用机制。
Sci Rep. 2020 Jun 1;10(1):8876. doi: 10.1038/s41598-020-65802-7.
5
Recent updates of marine antimicrobial peptides.海洋抗菌肽的最新进展
Saudi Pharm J. 2018 Mar;26(3):396-409. doi: 10.1016/j.jsps.2018.01.001. Epub 2018 Jan 4.
6
Mechanisms driving the antibacterial and antibiofilm properties of Hp1404 and its analogue peptides against multidrug-resistant Pseudomonas aeruginosa.驱动 Hp1404 及其类似肽对多药耐药铜绿假单胞菌的抗菌和抗生物膜特性的机制。
Sci Rep. 2018 Jan 29;8(1):1763. doi: 10.1038/s41598-018-19434-7.