期刊文献+

细胞穿膜肽的研究进展 被引量:10

Advance on the Research of Cell-Penetrating Peptides
原文传递
导出
摘要 目的综述细胞穿膜肽的研究进展。方法以近年来研究文献为基础,对细胞穿膜肽的结构特点、分类、内化机制、应用以及新的研究方向等进行综述。结果细胞穿膜肽(cell-penetrating peptides,CPPs)是一类由不多于30个氨基酸组成的小分子多肽,根据其氨基酸组成,可分为阳离子细胞穿膜肽和两亲性细胞穿膜肽。体内外研究表明,细胞穿膜肽能够介导多种载体的穿膜作用,无刺激性,并且在一定浓度范围内对宿主细胞无毒害作用。结论细胞穿膜肽的作用机制仍需进行深入探讨,但其作为一种新型药物递送工具,具有广泛的应用前景。 ObjectiveTo review the progress on cell-penetrating peptides(CPPs). Methods Based on the original researches in recent years, the structure properties, classification, internalization mechanism, application and novel research orientation of CPPs were introduced in the present paper. Results Cell-penetrating peptides(CPPs) consisted of 30 or less amino acids. CPPs, generally categorized as amphipathic or cationic depending on their sequences, are increasingly drawing attention as a non-invasive delivery technology for macromolecules. Delivery of a diverse set of cargoes has been attempted using different types of CPPs in vitro and in vivo. Additionally, the relative lack of toxicity and cell specificity has enabled its widespread use in preclinical models. This paper reviewed the studies on the structure properties, classification, internalization mechanism, application and novel research orientation of CPPs. Conclusion Although the internalization mechanism of CPPs will be studied deeply, CPPs, as a novel drug delivery tool, has promising application for the delivery of diverse drugs and cargoes.
出处 《中国药学杂志》 CAS CSCD 北大核心 2013年第14期1143-1147,共5页 Chinese Pharmaceutical Journal
基金 国家科技支撑计划资助项目(2008BAI55B03) 国家"重大新药创制"科技重大专项资助项目(2009ZX09310-004)
关键词 细胞穿膜肽 结构特点 分类 内化机制 cell-penetrating peptide, structure property, classification, internalization mechanism
  • 相关文献

参考文献34

  • 1ZARO J L,SHEN W C. Quantitative comparison of membrane trans- duction and endocytosis of oligopeptides [ J ]. Biochem Biophy Res Comm, 2003, 307(2) : 241-247.
  • 2WENDER P A, ROTHBARD J B, JESSOP T C, et al. Oligocar- bamate molecular transporters : Design, synthesis, and biological evaluation of a new class of transporters for drug delivery [ J ]. J Ame Chem Soc, 2002, 124(45) : 13382-13383.
  • 3FUTAKI S, NAKASE I, SUZUKI T, et al. Translocation of branched-chain arginine peptides through cell membranes'. Flexi- bility in the spatial disposition of positive charges in membrane- permeable peptides [ J ]. Biochemistry, 2002, 41 ( 25 ) : 7925- 7930.
  • 4FUTAKI S, SUZUKI T, OHASHI W, et al. Arginine-rich pep- tides. An abundant source of membrane-permeable peptides hav- ing potential as carriers for intracellular protein delivery[ J]. J Bi- ol Chem, 2001, 276: 5836-5840.
  • 5WENDER P A, MITCHELL D J, PATrABIRAMAN K, et al. The design, synthesis, and evaluation of molecules that enable or enhance cellular uptake: peptoid molecular transporters[ J]. Proc Natl Acad Sci USA, 2(130, 97(24) : 13003-13008.
  • 6MITCHELL D J, KIM D T, STEINMAN L, et al. Polyarginine enters ceils more efficiently than other polycationic homopolymers [J]. J Peptide Res, 2000, 56(5) : 318-325.
  • 7GUO Q G, ZHAO G J, HAO F J, et al. Effects of the TAT pep- tide orientation and relative location on the protein transduction ef- ficiency[J]. Chemical Biology & Drug Design, dio: 10. 1111/ j. 1747-0285. 2011. 01315. x.
  • 8KHAFAGY S EL, MORISHITA M, N, NISHIO R, et al. Structural requirements of penetratin absorption enhancement efficiency for in- sulin delivery[J]. J Controlled Release, 2010, 143(3) : 302-310.
  • 9LUNDBERG M, WIKSTROM S,JOHANSSON M. Cell surface adherence and endocytosis of protein transduction domains [ J ]. Mole Ther, 2003, 8(1) : 143-150.
  • 10HERCE H D, GARCIA A E, L1TY J, et al. Arginine-rich pep- tides destabilize the plasma membrane, consistent with a pore for- mation translocation mechanism of cell-penetrating peptides [ J ]. Biophy J, 2009, 97 : 1917-1925.

二级参考文献2

共引文献8

同被引文献65

  • 1黄开红,王凌云,赵晓龙,刘建化,陈汝福,朱兆华.抗VEGF单克隆抗体偶联5-FU纳米微粒的初步研究[J].中国病理生理杂志,2007,23(2):258-261. 被引量:15
  • 2崔福德.药剂学[M] .7版.北京:人民卫生出版社,2011:197-198.
  • 3Lo CL,Lin KM, Hsiue GH, et al. Preparation and char- acterization of intelligent core- shell nanoparticles based on poly ( d. l-lactide)-g-poly ( N-isopropyl acrylamid-co- metha-crylic acid) [J]. J Control Release, 2005,104 ( 3 ) : 477-449.
  • 4Nikolay A. Brusentsov, Tatiana NB, Elena YF, et al. Magneto-hydrodynamic thermochemotherapy and MRI of mouse tumor[J]. J Magn Magp. Mater, 2007, 311 (1) :176-180.
  • 5Zur Muhlen A, Sehwarz C, Mehnert W. Solid lipid nano- particlar(SLN) for controlled drug delivery-drug release and release mechanism [J]. Eur J pharm Biopharm, 2006,47(3) : 147-152.
  • 6Li CY. The research of liver targeted dosage system [J]. Emerg Tradchin Med(Chinese), 2001,10 ( 6 ) : 354- 356.
  • 7Young SC,Allan ED. Cell Penetrating Peptides and the Mechanisms for Intracellular EntryEJ2. Current Phar- maceutical Bioteehnology, 2014,5(3) : 192-199.
  • 8Ofelia Maniti, Hong-Rong Piao, Jesus Ayala Sanmar tin. Basic cell penetrating peptides induce plasma mem- brane positive curvature, lipid domain separation and protein redistribution [J]. International Journal of Bio-chemistry and Cell Biology,2014,50(3) 73-81.
  • 9Khaleel Khaja,Paul Robbins. Comparison of Functional Protein Transduction Domains Using the NEMO Bind- ing Domain Peptide[J]. Pharmaceuticals, 2010,3 ( 1 ) : 110-115.
  • 10Javier Sanchez-Nievesa, Peter Fransene, Daniel Pulido, et al. Amphiphilic Cationic Carbosilane-PEG Dendrim- ers: Synthesis and Applications in Gene Therapy [J]. European Journal of Medicinal Chemistry, 2014,76 (9) : 43-52.

引证文献10

二级引证文献15

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部