• 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

使用细胞穿透肽的细胞内转导

Intracellular transduction using cell-penetrating peptides.

作者信息

Sawant Rupa, Torchilin Vladimir

机构信息

Department of Pharmaceutical Sciences and Center for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University, Mugar Building, Room 312, 360 Huntington Avenue, Boston, MA 02115, USA.

出版信息

Mol Biosyst. 2010 Apr;6(4):628-40. doi: 10.1039/b916297f. Epub 2009 Dec 21.

DOI:10.1039/b916297f
PMID:20237640
Abstract

Cell penetrating peptides (CPPs), TATp, in particular, has been used widely for intracellular delivery of various agents ranging from small molecules to proteins, peptides, range of pharmaceutical nanocarriers and imaging agents. This review highlights the mechanisms of CPP-mediated delivery and summarizes numerous examples illustrating the potential of CPPs in the fields of biology and medicine.

摘要

细胞穿透肽(CPPs),尤其是TATp,已被广泛用于将各种物质进行细胞内递送,这些物质范围从小分子到蛋白质、肽、一系列药物纳米载体和成像剂。本综述重点介绍了CPP介导递送的机制,并总结了大量实例,阐明了CPPs在生物学和医学领域的潜力。

相似文献

1
Intracellular transduction using cell-penetrating peptides.使用细胞穿透肽的细胞内转导
Mol Biosyst. 2010 Apr;6(4):628-40. doi: 10.1039/b916297f. Epub 2009 Dec 21.
2
Intracellular cargo delivery using tat peptide and derivatives.使用tat肽及其衍生物进行细胞内货物递送。
Med Res Rev. 2004 Jan;24(1):1-12. doi: 10.1002/med.10056.
3
Transport molecules using reverse sequence HIV-Tat polypeptides: not just any old Tat? (WO200808225).使用反向序列HIV-Tat多肽转运分子:只是普通的Tat吗?(WO200808225)
Expert Opin Ther Pat. 2009 Sep;19(9):1329-33. doi: 10.1517/17530050902824829.
4
The augmentation of intracellular delivery of peptide therapeutics by artificial protein transduction domains.人工蛋白质转导结构域增强肽类治疗药物的细胞内递送
Biomaterials. 2009 Jul;30(19):3318-23. doi: 10.1016/j.biomaterials.2009.02.031. Epub 2009 Mar 21.
5
The cationic cell-penetrating peptide CPP(TAT) derived from the HIV-1 protein TAT is rapidly transported into living fibroblasts: optical, biophysical, and metabolic evidence.源自HIV-1蛋白TAT的阳离子细胞穿透肽CPP(TAT)能迅速转运到活的成纤维细胞中:光学、生物物理及代谢证据。
Biochemistry. 2005 Jan 11;44(1):138-48. doi: 10.1021/bi0491604.
6
Cell penetrating peptide-modified pharmaceutical nanocarriers for intracellular drug and gene delivery.用于细胞内药物和基因递送的细胞穿透肽修饰的药物纳米载体。
Biopolymers. 2008;90(5):604-10. doi: 10.1002/bip.20989.
7
Intracellular delivery of nanoparticles with CPPs.通过细胞穿透肽实现纳米颗粒的细胞内递送。
Methods Mol Biol. 2011;683:431-51. doi: 10.1007/978-1-60761-919-2_31.
8
Inhibition of platelet activation by peptide analogs of the beta(3)-intracellular domain of platelet integrin alpha(IIb)beta(3) conjugated to the cell-penetrating peptide Tat(48-60).通过与穿膜肽 Tat(48-60)偶联的血小板整合素 α(IIb)β(3)胞内域的β(3)肽模拟物抑制血小板活化。
Platelets. 2009 Dec;20(8):539-47. doi: 10.3109/09537100903324219.
9
Tat(48-60) peptide amino acid sequence is not unique in its cell penetrating properties and cell-surface glycosaminoglycans inhibit its cellular uptake.Tat(48-60)肽的氨基酸序列在其穿透细胞的特性方面并不是独一无二的,细胞表面的糖胺聚糖会抑制其细胞摄取。
J Control Release. 2012 Mar 10;158(2):277-85. doi: 10.1016/j.jconrel.2011.11.007. Epub 2011 Nov 12.
10
Intracellular delivery of large molecules and small particles by cell-penetrating proteins and peptides.通过细胞穿透蛋白和肽实现大分子和小颗粒的细胞内递送。
Adv Drug Deliv Rev. 2005 Feb 28;57(4):637-51. doi: 10.1016/j.addr.2004.10.007. Epub 2004 Dec 22.

引用本文的文献

1
Advancements in Transdermal Drug Delivery Systems: Harnessing the Potential of Macromolecular Assisted Permeation Enhancement and Novel Techniques.透皮给药系统的进展:利用大分子辅助渗透增强和新技术的潜力。
AAPS PharmSciTech. 2025 Jan 9;26(1):29. doi: 10.1208/s12249-024-03029-9.
2
Delivery of Various Cargos into Cancer Cells and Tissues via Cell-Penetrating Peptides: A Review of the Last Decade.通过细胞穿透肽将各种货物递送至癌细胞和组织:过去十年综述
Pharmaceutics. 2021 Sep 2;13(9):1391. doi: 10.3390/pharmaceutics13091391.
3
Versatility of cell-penetrating peptides for intracellular delivery of siRNA.
细胞穿透肽在 siRNA 细胞内递送中的多功能性。
Drug Deliv. 2018 Nov;25(1):1996-2006. doi: 10.1080/10717544.2018.1543366.
4
Deepened cellular/subcellular interface penetration and enhanced antitumor efficacy of cyclic peptidic ligand-decorated accelerating active targeted nanomedicines.环状肽配体修饰的加速主动靶向纳米药物增强细胞/亚细胞界面穿透并提高抗肿瘤疗效。
Int J Nanomedicine. 2018 Sep 19;13:5537-5559. doi: 10.2147/IJN.S172556. eCollection 2018.
5
Improved method for synthesis of low molecular weight protamine-siRNA conjugate.低分子量鱼精蛋白-siRNA 偶联物的改进合成方法。
Acta Pharm Sin B. 2018 Jan;8(1):116-126. doi: 10.1016/j.apsb.2017.11.011. Epub 2017 Dec 19.
6
Transferrin and octaarginine modified dual-functional liposomes with improved cancer cell targeting and enhanced intracellular delivery for the treatment of ovarian cancer.转铁蛋白和八精氨酸修饰的双功能脂质体,改善了癌细胞靶向性并增强了细胞内递药,用于卵巢癌治疗。
Drug Deliv. 2018 Nov;25(1):517-532. doi: 10.1080/10717544.2018.1435747.
7
Cell Penetrating Peptides as Molecular Carriers for Anti-Cancer Agents.细胞穿透肽作为抗癌药物的分子载体。
Molecules. 2018 Jan 31;23(2):295. doi: 10.3390/molecules23020295.
8
Plant Ribosome-Inactivating Proteins: Progesses, Challenges and Biotechnological Applications (and a Few Digressions).植物核糖体失活蛋白:进展、挑战和生物技术应用(及一些题外话)。
Toxins (Basel). 2017 Oct 12;9(10):314. doi: 10.3390/toxins9100314.
9
High-Yield Synthesis of Monomeric LMWP(CPP)-siRNA Covalent Conjugate for Effective Cytosolic Delivery of siRNA.用于有效胞质递送小干扰RNA的单体低分子量富含脯氨酸的蛋白质(CPP)-小干扰RNA共价缀合物的高产率合成
Theranostics. 2017 Jun 25;7(9):2495-2508. doi: 10.7150/thno.19863. eCollection 2017.
10
Improved Protein Toxin Delivery Based on ATTEMPTS Systems.基于 ATTEMPTS 系统的改良蛋白毒素递呈。
Curr Drug Targets. 2018 Feb 19;19(4):380-392. doi: 10.2174/1389450118666170302094758.