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本文引用的文献

1
Improved potency and reduced toxicity of the antifungal peptoid AEC5 through submonomer modification.通过亚单体修饰提高抗真菌类肽AEC5的效力并降低其毒性。
Bioorg Med Chem Lett. 2018 Dec 1;28(22):3514-3519. doi: 10.1016/j.bmcl.2018.10.001. Epub 2018 Oct 3.
2
Exploring the links between peptoid antibacterial activity and toxicity.探索类肽抗菌活性与毒性之间的联系。
Medchemcomm. 2017 Feb 1;8(5):886-896. doi: 10.1039/c6md00648e. eCollection 2017 May 1.
3
Peeling the onion: the outer layers of Cryptococcus neoformans.剖析新型隐球菌:外层结构
Mem Inst Oswaldo Cruz. 2018;113(7):e180040. doi: 10.1590/0074-02760180040. Epub 2018 May 7.
4
Hydrophobic interactions modulate antimicrobial peptoid selectivity towards anionic lipid membranes.疏水性相互作用调节抗菌肽类似物对阴离子脂质膜的选择性。
Biochim Biophys Acta Biomembr. 2018 Jun;1860(6):1414-1423. doi: 10.1016/j.bbamem.2018.03.021. Epub 2018 Apr 3.
5
Advances in Development of Antimicrobial Peptidomimetics as Potential Drugs.抗菌肽模拟物作为潜在药物的研究进展。
Molecules. 2017 Aug 29;22(9):1430. doi: 10.3390/molecules22091430.
6
The Fungal Cell Wall: Structure, Biosynthesis, and Function.真菌细胞壁:结构、生物合成与功能。
Microbiol Spectr. 2017 May;5(3). doi: 10.1128/microbiolspec.FUNK-0035-2016.
7
Global burden of disease of HIV-associated cryptococcal meningitis: an updated analysis.HIV 相关隐球菌性脑膜炎的全球疾病负担:最新分析
Lancet Infect Dis. 2017 Aug;17(8):873-881. doi: 10.1016/S1473-3099(17)30243-8. Epub 2017 May 5.
8
Evaluating the Effect of Peptoid Lipophilicity on Antimicrobial Potency, Cytotoxicity, and Combinatorial Library Design.评估类肽亲脂性对抗菌效力、细胞毒性及组合文库设计的影响。
ACS Comb Sci. 2017 Apr 10;19(4):229-233. doi: 10.1021/acscombsci.7b00007. Epub 2017 Mar 16.
9
Peptoids successfully inhibit the growth of gram negative E. coli causing substantial membrane damage.肽缩氨酸成功抑制革兰氏阴性大肠杆菌的生长,导致大量膜损伤。
Sci Rep. 2017 Feb 14;7:42332. doi: 10.1038/srep42332.
10
Discovery and Characterization of a Peptoid with Antifungal Activity against .一种对……具有抗真菌活性的类肽的发现与特性研究
ACS Med Chem Lett. 2016 Oct 3;7(12):1139-1144. doi: 10.1021/acsmedchemlett.6b00338. eCollection 2016 Dec 8.

朝着临床抗真菌肽的方向:对 AEC5 治疗潜力的研究。

Toward a clinical antifungal peptoid: Investigations into the therapeutic potential of AEC5.

机构信息

Department of Chemistry, Middle Tennessee State University, Murfreesboro, Tennessee.

Department of Biology, Middle Tennessee State University, Murfreesboro, Tennessee.

出版信息

Biopolymers. 2019 Jun;110(6):e23276. doi: 10.1002/bip.23276. Epub 2019 Apr 2.

DOI:10.1002/bip.23276
PMID:30938841
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6660985/
Abstract

Cryptococcus neoformans is a fungal pathogen that causes cryptococcal meningitis in immunocompromised individuals. Existing antifungal treatment plans have high mammalian toxicity and increasing drug resistance, demonstrating the dire need for new, nontoxic therapeutics. Antimicrobial peptoids are one alternative to combat this issue. Our lab has recently identified a tripeptoid, AEC5, with promising efficacy and selectivity against C. neoformans. Here, we report studies into the broad-spectrum efficacy, killing kinetics, mechanism of action, in vivo half-life, and subchronic toxicity of this compound. Most notably, these studies have demonstrated that AEC5 rapidly reduces fungal burden, killing all viable fungi within 3 hours. Additionally, AEC5 has an in vivo half-life of 20+ hours and no observable in vivo toxicity following 28 days of daily injections. This research represents an important step in the characterization of AEC5 as a practical treatment option against C. neoformans infections.

摘要

新型隐球菌是一种真菌病原体,可导致免疫功能低下个体发生隐球菌性脑膜炎。现有的抗真菌治疗方案具有较高的哺乳动物毒性和不断增加的耐药性,这迫切需要开发新的、无毒的治疗方法。抗菌肽是解决这一问题的一种替代方法。我们实验室最近发现了一种三肽,AEC5,对新型隐球菌具有有前景的疗效和选择性。在这里,我们报告了这项化合物的广谱疗效、杀菌动力学、作用机制、体内半衰期和亚慢性毒性研究。值得注意的是,这些研究表明 AEC5 能迅速降低真菌负荷,在 3 小时内杀死所有存活的真菌。此外,AEC5 的体内半衰期超过 20 小时,并且在 28 天的每日注射后没有观察到体内毒性。这项研究代表了将 AEC5 作为一种针对新型隐球菌感染的实用治疗选择进行特征描述的重要一步。