• 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

NP339 的初步特征:一种具有广谱抗真菌活性的新型多精氨酸肽。

Preliminary Characterization of NP339, a Novel Polyarginine Peptide with Broad Antifungal Activity.

机构信息

NovaBiotics, Ltd., Aberdeen, United Kingdom.

The University of Aberdeen, Institute of Medical Sciences, Aberdeen, United Kingdom.

出版信息

Antimicrob Agents Chemother. 2021 Jul 16;65(8):e0234520. doi: 10.1128/AAC.02345-20.

DOI:10.1128/AAC.02345-20
PMID:34031048
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8284473/
Abstract

Fungi cause disease in nearly one billion individuals worldwide. Only three classes of antifungal agents are currently available in mainstream clinical use. Emerging and drug-resistant fungi, toxicity, and drug-drug interactions compromise their efficacy and applicability. Consequently, new and improved antifungal therapies are urgently needed. In response to that need, we have developed NP339, a 2-kDa polyarginine peptide that is active against pathogenic fungi from the genera , Aspergillus, and Cryptococcus, as well as others. NP339 was designed based on endogenous cationic human defense peptides, which are constituents of the cornerstone of immune defense against pathogenic microbes. NP339 specifically targets the fungal cell membrane through a charge-charge-initiated membrane interaction and therefore possesses a differentiated safety and toxicity profile to existing antifungal classes. NP339 is rapidly fungicidal and does not elicit resistance in target fungi upon extensive passaging . Preliminary analyses in murine models indicate scope for therapeutic application of NP339 against a range of systemic and mucocutaneous fungal infections. Collectively, these data indicate that NP339 can be developed into a highly differentiated, first-in-class antifungal candidate for poorly served invasive and other serious fungal diseases.

摘要

真菌在全球范围内导致近 10 亿人患病。目前在主流临床应用中只有三类抗真菌药物。新兴的和耐药的真菌、毒性和药物相互作用影响了它们的疗效和适用性。因此,迫切需要新的和改进的抗真菌疗法。针对这一需求,我们开发了 NP339,这是一种 2kDa 的多精氨酸肽,对 属、 和 属的致病真菌以及其他真菌具有活性。NP339是基于内源性阳离子人防御肽设计的,这些肽是针对致病微生物的免疫防御基石的组成部分。NP339通过电荷引发的膜相互作用特异性靶向真菌细胞膜,因此具有与现有抗真菌药物不同的安全性和毒性特征。NP339具有快速杀菌作用,并且在广泛传代后不会在目标真菌中引起耐药性。在小鼠模型中的初步分析表明,NP339在治疗一系列系统性和粘膜真菌感染方面具有应用潜力。总的来说,这些数据表明,NP339可以开发成一种高度差异化的、首创的抗真菌候选药物,用于治疗服务不足的侵袭性和其他严重真菌病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e69/8284473/ee3f74e66e46/aac.02345-20-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e69/8284473/f2225bbc5d27/aac.02345-20-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e69/8284473/0d389d19e30c/aac.02345-20-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e69/8284473/e50ee81102b2/aac.02345-20-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e69/8284473/224f9b72f3a1/aac.02345-20-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e69/8284473/4bfa597b3ed3/aac.02345-20-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e69/8284473/ee3f74e66e46/aac.02345-20-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e69/8284473/f2225bbc5d27/aac.02345-20-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e69/8284473/0d389d19e30c/aac.02345-20-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e69/8284473/e50ee81102b2/aac.02345-20-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e69/8284473/224f9b72f3a1/aac.02345-20-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e69/8284473/4bfa597b3ed3/aac.02345-20-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e69/8284473/ee3f74e66e46/aac.02345-20-f0006.jpg

相似文献

1
Preliminary Characterization of NP339, a Novel Polyarginine Peptide with Broad Antifungal Activity.NP339 的初步特征:一种具有广谱抗真菌活性的新型多精氨酸肽。
Antimicrob Agents Chemother. 2021 Jul 16;65(8):e0234520. doi: 10.1128/AAC.02345-20.
2
A host defense peptide mimetic, brilacidin, potentiates caspofungin antifungal activity against human pathogenic fungi.一种宿主防御肽模拟物,溴硝醇,增强了卡泊芬净抗真菌活性,针对人类致病性真菌。
Nat Commun. 2023 Apr 12;14(1):2052. doi: 10.1038/s41467-023-37573-y.
3
Peptide-Like Nylon-3 Polymers with Activity against Phylogenetically Diverse, Intrinsically Drug-Resistant Pathogenic Fungi.具有抗系统发育多样化、固有耐药性致病真菌活性的肽状尼龙-3 聚合物。
mSphere. 2018 May 23;3(3). doi: 10.1128/mSphere.00223-18. eCollection 2018 May-Jun.
4
Caspofungin: pharmacology, safety and therapeutic potential in superficial and invasive fungal infections.卡泊芬净:在浅表和侵袭性真菌感染中的药理学、安全性及治疗潜力
Expert Opin Investig Drugs. 2001 Aug;10(8):1545-58. doi: 10.1517/13543784.10.8.1545.
5
A Cationic Polymer That Shows High Antifungal Activity against Diverse Human Pathogens.一种对多种人体病原体具有高抗真菌活性的阳离子聚合物。
Antimicrob Agents Chemother. 2017 Sep 22;61(10). doi: 10.1128/AAC.00204-17. Print 2017 Oct.
6
[In vitro antifungal activity of voriconazole: New data after the first years of clinical experience].伏立康唑的体外抗真菌活性:临床应用首年之后的新数据
Rev Iberoam Micol. 2007 Sep 30;24(3):198-208. doi: 10.1016/s1130-1406(07)70043-8.
7
Oxadiazole-Containing Macrocyclic Peptides Potentiate Azole Activity against Pathogenic Species.含恶二唑的大环肽增强唑类药物对致病性物种的活性。
mSphere. 2020 Apr 8;5(2):e00256-20. doi: 10.1128/mSphere.00256-20.
8
New antifungal agents.新型抗真菌药物。
Dermatol Clin. 2003 Jul;21(3):565-76. doi: 10.1016/s0733-8635(03)00024-x.
9
Antifungal Activity, Toxicity, and Membranolytic Action of a Mastoparan Analog Peptide.一种蜂毒素类似肽的抗真菌活性、毒性和膜溶作用。
Front Cell Infect Microbiol. 2019 Dec 6;9:419. doi: 10.3389/fcimb.2019.00419. eCollection 2019.
10
[In vitro antifungal activity of micafungin].[米卡芬净的体外抗真菌活性]
Rev Iberoam Micol. 2009 Mar 31;26(1):35-41. doi: 10.1016/S1130-1406(09)70006-3. Epub 2009 May 7.

引用本文的文献

1
Pharmacokinetic and ADMET Profiles of Synthetic Antimicrobial Peptides (AMPs).合成抗菌肽(AMPs)的药代动力学和ADMET特性
Mini Rev Med Chem. 2025;25(8):579-590. doi: 10.2174/0113895575362479241231054240.
2
Antimicrobial Peptides: A Promising Alternative to Conventional Antimicrobials for Combating Polymicrobial Biofilms.抗菌肽:对抗多种微生物生物膜的传统抗菌药物的一种有前景的替代物。
Adv Sci (Weinh). 2025 Jan;12(1):e2410893. doi: 10.1002/advs.202410893. Epub 2024 Nov 12.
3
Oligoarginine peptide structure and its effect on cell penetration in ocular drug delivery.

本文引用的文献

1
Antimicrobial Susceptibility Testing of Antimicrobial Peptides to Better Predict Efficacy.抗菌肽的药敏试验以更好地预测疗效。
Front Cell Infect Microbiol. 2020 Jul 7;10:326. doi: 10.3389/fcimb.2020.00326. eCollection 2020.
2
Antimicrobial peptides: Application informed by evolution.抗菌肽:进化启示下的应用。
Science. 2020 May 1;368(6490). doi: 10.1126/science.aau5480.
3
Pharmacokinetics and Pharmacodynamics of Posaconazole.泊沙康唑的药代动力学和药效学。
寡聚精氨酸肽结构及其在眼部药物递送中对细胞穿透的影响。
Heliyon. 2024 Jul 24;10(15):e35109. doi: 10.1016/j.heliyon.2024.e35109. eCollection 2024 Aug 15.
4
Insights from Three Pan-European Multicentre Studies on Invasive Candida Infections and Outlook to ECMM Candida IV.三项关于侵袭性念珠菌感染的泛欧多中心研究的见解及欧洲临床微生物与感染病学会念珠菌IV会议展望
Mycopathologia. 2024 Aug 1;189(4):70. doi: 10.1007/s11046-024-00871-0.
5
Exploring the frontiers of therapeutic breadth of antifungal peptides: A new avenue in antifungal drugs.探索抗真菌肽治疗广度的前沿:抗真菌药物的新途径。
J Ind Microbiol Biotechnol. 2024 Jan 9;51. doi: 10.1093/jimb/kuae018.
6
Antifungal Activities of L-Methionine and L-Arginine Treatment In Vitro and In Vivo against .L-蛋氨酸和L-精氨酸体外及体内抗……的抗真菌活性
Microorganisms. 2024 Feb 9;12(2):360. doi: 10.3390/microorganisms12020360.
7
Antimicrobial Peptides: Avant-Garde Antifungal Agents to Fight against Medically Important Species.抗菌肽:对抗医学上重要真菌物种的先锋抗真菌剂。
Pharmaceutics. 2023 Feb 27;15(3):789. doi: 10.3390/pharmaceutics15030789.
8
The Activity of Polyhomoarginine against .聚高聚精氨酸对……的活性
Biology (Basel). 2022 Nov 28;11(12):1726. doi: 10.3390/biology11121726.
9
COVID-19-Associated Fungal Infections: An Urgent Need for Alternative Therapeutic Approach?新型冠状病毒肺炎相关真菌感染:是否迫切需要替代治疗方法?
Front Microbiol. 2022 Jun 9;13:919501. doi: 10.3389/fmicb.2022.919501. eCollection 2022.
10
Invasive candidiasis: investigational drugs in the clinical development pipeline and mechanisms of action.侵袭性念珠菌病:临床开发管道中的研究药物及作用机制。
Expert Opin Investig Drugs. 2022 Aug;31(8):795-812. doi: 10.1080/13543784.2022.2086120. Epub 2022 Jun 15.
Drugs. 2020 May;80(7):671-695. doi: 10.1007/s40265-020-01306-y.
4
Aspiring Antifungals: Review of Current Antifungal Pipeline Developments.有潜力的抗真菌药物:当前抗真菌药物研发进展综述
J Fungi (Basel). 2020 Feb 25;6(1):28. doi: 10.3390/jof6010028.
5
Antimicrobial Peptides: Virulence and Resistance Modulation in Gram-Negative Bacteria.抗菌肽:革兰氏阴性菌中毒力与耐药性的调节
Microorganisms. 2020 Feb 19;8(2):280. doi: 10.3390/microorganisms8020280.
6
Expression and Function of Host Defense Peptides at Inflammation Sites.炎症部位宿主防御肽的表达和功能。
Int J Mol Sci. 2019 Dec 22;21(1):104. doi: 10.3390/ijms21010104.
7
Aspergillus fumigatus Clinical Isolates Carrying CYP51A with TR34/L98H/S297T/F495I Substitutions Detected after Four-Year Retrospective Azole Resistance Screening in Brazil.巴西四年回顾性唑类药物耐药性筛查后检测到携带 CYP51A 的 TR34/L98H/S297T/F495I 取代的烟曲霉临床分离株。
Antimicrob Agents Chemother. 2020 Feb 21;64(3). doi: 10.1128/AAC.02059-19.
8
Facilitators of adaptation and antifungal resistance mechanisms in clinically relevant fungi.临床上相关真菌的适应性和抗真菌耐药机制的促进因素。
Fungal Genet Biol. 2019 Nov;132:103254. doi: 10.1016/j.fgb.2019.103254. Epub 2019 Jul 19.
9
Antibiotic Discovery: Where Have We Come from, Where Do We Go?抗生素发现:我们来自何处,将去往何方?
Antibiotics (Basel). 2019 Apr 24;8(2):45. doi: 10.3390/antibiotics8020045.
10
The Hidden Cost of Modern Medical Interventions: How Medical Advances Have Shaped the Prevalence of Human Fungal Disease.现代医学干预的隐性成本:医学进步如何塑造人类真菌病的流行率
Pathogens. 2019 Apr 4;8(2):45. doi: 10.3390/pathogens8020045.