• 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

药物设计中的组合肽库:来自有毒芋螺的经验教训。

Combinatorial peptide libraries in drug design: lessons from venomous cone snails.

作者信息

Olivera B M, Hillyard D R, Marsh M, Yoshikami D

机构信息

Department of Biology, University of Utah, Salt Lake City 84112, USA.

出版信息

Trends Biotechnol. 1995 Oct;13(10):422-6. doi: 10.1016/S0167-7799(00)88996-9.

DOI:10.1016/S0167-7799(00)88996-9
PMID:7546566
Abstract

Many present-day drugs are derived from compounds that are natural products, a traditional source of which is fermentation broths of microorganisms. The venoms of cone snails are a new natural resource of peptides that may have a pharmaceutical potential equivalent to those from traditional sources, particularly for developing drugs that target cell-surface receptors or ion channels. In effect, cone snails have used a combinatorial library strategy to evolve their small, highly bioactive venom peptides. The methods by which the snails have generated thousands of peptides with remarkable specificity and high affinity for their targets may provide important lessons in designing combinatorial libraries for drug development.

摘要

许多现代药物都源自天然产物化合物,其传统来源是微生物发酵液。芋螺毒液是一种新的肽类天然资源,其药用潜力可能与传统来源的相当,尤其适用于开发针对细胞表面受体或离子通道的药物。实际上,芋螺采用了组合文库策略来进化其小的、高生物活性的毒液肽。芋螺产生数千种对其靶标具有显著特异性和高亲和力的肽的方法,可能会为设计用于药物开发的组合文库提供重要借鉴。

相似文献

1
Combinatorial peptide libraries in drug design: lessons from venomous cone snails.药物设计中的组合肽库:来自有毒芋螺的经验教训。
Trends Biotechnol. 1995 Oct;13(10):422-6. doi: 10.1016/S0167-7799(00)88996-9.
2
Drugs from the peptide venoms of marine cone shells.来自海洋芋螺肽毒液的药物。
Australas Biotechnol. 1994 Sep-Oct;4(5):298-300.
3
Molecular prospecting for drugs from the sea. Isolating therapeutic peptides and proteins from cone snail venom.从海洋中进行药物的分子勘探。从芋螺毒液中分离治疗性肽和蛋白质。
IEEE Eng Med Biol Mag. 2005 Mar-Apr;24(2):79-84. doi: 10.1109/memb.2005.1411352.
4
Venomous auger snail Hastula (Impages) hectica (Linnaeus, 1758): molecular phylogeny, foregut anatomy and comparative toxinology.有毒的钻螺哈氏骨螺(Impages)hectica(林奈,1758年):分子系统发育、前肠解剖学与比较毒素学
J Exp Zool B Mol Dev Evol. 2007 Dec 15;308(6):744-56. doi: 10.1002/jez.b.21195.
5
Novel pharmacological targets from Indian cone snails.新型药理学靶点:来自印度芋螺。
Mini Rev Med Chem. 2011 Feb;11(2):125-30. doi: 10.2174/138955711794519500.
6
Identification of neuropeptide Y-like conopeptides from the venom of Conus betulinus.鉴定来自褐云玛瑙螺毒液的神经肽 Y 样芋螺肽。
Acta Biochim Biophys Sin (Shanghai). 2010 Jul;42(7):502-5. doi: 10.1093/abbs/gmq042. Epub 2010 Jun 8.
7
Novel peptides of therapeutic promise from Indian Conidae.来自印度芋螺科具有治疗前景的新型肽。
Ann N Y Acad Sci. 2005 Nov;1056:462-73. doi: 10.1196/annals.1352.022.
8
Structural and biosynthetic properties of peptides in cone snail venoms.芋螺毒液中肽的结构与生物合成特性。
Peptides. 1995;16(6):1007-17. doi: 10.1016/0196-9781(95)00086-y.
9
Direct cDNA cloning of novel conopeptide precursors of the O-superfamily.O超家族新型芋螺肽前体的直接cDNA克隆
Peptides. 2005 Mar;26(3):361-7. doi: 10.1016/j.peptides.2004.10.027.
10
Marine snail venoms: use and trends in receptor and channel neuropharmacology.海蜗牛毒液:受体与通道神经药理学中的应用及趋势
Curr Opin Pharmacol. 2009 Oct;9(5):594-601. doi: 10.1016/j.coph.2009.05.006. Epub 2009 Jun 18.

引用本文的文献

1
Potent painkiller from spider venom antagonizes P2X3 receptors without dysgeusia.源自蜘蛛毒液的强效止痛药可拮抗P2X3受体且无味觉障碍。
Mol Ther. 2025 Feb 5;33(2):771-785. doi: 10.1016/j.ymthe.2024.12.036. Epub 2024 Dec 31.
2
Stabilizing Scaffold for Short Peptides Based on Knottins.基于结蛋白的短肽稳定支架
Curr Cancer Drug Targets. 2024;24(12):1275-1285. doi: 10.2174/0115680096285288240118090050.
3
The deep-rooted origin of disulfide-rich spider venom toxins.富含二硫键的蜘蛛毒液毒素的深远起源。
Elife. 2023 Feb 9;12:e83761. doi: 10.7554/eLife.83761.
4
Principal Component and Structural Element Analysis Provide Insights into the Evolutionary Divergence of Conotoxins.主成分分析和结构元件分析为芋螺毒素的进化分歧提供了见解。
Biology (Basel). 2022 Dec 22;12(1):20. doi: 10.3390/biology12010020.
5
Potassium channel blocker crafted by α-hairpinin scaffold engineering.由α-发夹素支架工程构建的钾通道阻滞剂。
Biophys J. 2021 Jun 15;120(12):2471-2481. doi: 10.1016/j.bpj.2021.04.020. Epub 2021 Apr 29.
6
α-Conotoxin Peptidomimetics: Probing the Minimal Binding Motif for Effective Analgesia.α-芋螺毒素肽拟肽:探究有效镇痛的最小结合基序。
Toxins (Basel). 2020 Aug 6;12(8):505. doi: 10.3390/toxins12080505.
7
Animal toxins - Nature's evolutionary-refined toolkit for basic research and drug discovery.动物毒素——大自然进化完善的基础研究和药物发现工具包。
Biochem Pharmacol. 2020 Nov;181:114096. doi: 10.1016/j.bcp.2020.114096. Epub 2020 Jun 12.
8
Selective spider toxins reveal a role for the Nav1.1 channel in mechanical pain.选择性蜘蛛毒素揭示了Nav1.1通道在机械性疼痛中的作用。
Nature. 2016 Jun 23;534(7608):494-9. doi: 10.1038/nature17976. Epub 2016 Jun 6.
9
Combinatorial biosynthesis of RiPPs: docking with marine life.核糖体合成和翻译后修饰肽(RiPPs)的组合生物合成:与海洋生物的对接
Curr Opin Chem Biol. 2016 Apr;31:15-21. doi: 10.1016/j.cbpa.2015.11.016. Epub 2015 Dec 19.
10
The Cystine Knot Is Responsible for the Exceptional Stability of the Insecticidal Spider Toxin ω-Hexatoxin-Hv1a.胱氨酸结赋予杀虫蜘蛛毒素ω-六聚毒素-Hv1a非凡的稳定性。
Toxins (Basel). 2015 Oct 26;7(10):4366-80. doi: 10.3390/toxins7104366.