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Evaluation of a cell penetrating prenylated peptide lacking an intrinsic fluorophore via in situ click reaction.通过原位点击反应评估缺乏内在荧光团的细胞穿透型 prenylated 肽。
Bioorg Med Chem Lett. 2011 Sep 1;21(17):4998-5001. doi: 10.1016/j.bmcl.2011.04.138. Epub 2011 May 6.
7
Enlarging the scope of cell-penetrating prenylated peptides to include farnesylated 'CAAX' box sequences and diverse cell types.将穿膜异戊二烯化肽的作用范围扩大到包括法尼基化的 'CAAX' 框序列和多种细胞类型。
Chem Biol Drug Des. 2010 Aug;76(2):107-15. doi: 10.1111/j.1747-0285.2010.00992.x. Epub 2010 Jun 23.

本文引用的文献

1
Multifunctional prenylated peptides for live cell analysis.用于活细胞分析的多功能异戊烯化肽
J Am Chem Soc. 2009 Jun 3;131(21):7293-303. doi: 10.1021/ja805174z.
2
Predicting cell-penetrating peptides.预测细胞穿透肽。
Adv Drug Deliv Rev. 2008 Mar 1;60(4-5):572-9. doi: 10.1016/j.addr.2007.09.003. Epub 2007 Oct 22.
3
Hydrophilic anilinogeranyl diphosphate prenyl analogues are Ras function inhibitors.亲水性苯胺基香叶基二磷酸异戊二烯类似物是Ras功能抑制剂。
Biochemistry. 2006 Dec 26;45(51):15862-72. doi: 10.1021/bi061704+. Epub 2006 Dec 6.
4
The engineering of membrane-permeable peptides.可穿透细胞膜的肽的工程设计。
Anal Biochem. 2005 Jun 15;341(2):290-8. doi: 10.1016/j.ab.2005.03.026.
5
Membrane translocation of penetratin and its derivatives in different cell lines.穿膜肽及其衍生物在不同细胞系中的膜转位
J Mol Recognit. 2003 Sep-Oct;16(5):272-9. doi: 10.1002/jmr.637.
6
Direct visualization by confocal fluorescent microscopy of the permeation of myristoylated peptides through the cell membrane.通过共聚焦荧光显微镜直接观察肉豆蔻酰化肽透过细胞膜的过程。
IUBMB Life. 2002 Jul;54(1):33-6. doi: 10.1080/15216540213823.
7
Differential localization of Rho GTPases in live cells: regulation by hypervariable regions and RhoGDI binding.Rho GTP酶在活细胞中的差异定位:由高变区和RhoGDI结合进行调控
J Cell Biol. 2001 Jan 8;152(1):111-26. doi: 10.1083/jcb.152.1.111.
8
The design, synthesis, and evaluation of molecules that enable or enhance cellular uptake: peptoid molecular transporters.能够实现或增强细胞摄取的分子的设计、合成及评估:类肽分子转运体
Proc Natl Acad Sci U S A. 2000 Nov 21;97(24):13003-8. doi: 10.1073/pnas.97.24.13003.
9
Protein-damaging stresses activate c-Jun N-terminal kinase via inhibition of its dephosphorylation: a novel pathway controlled by HSP72.蛋白质损伤应激通过抑制其去磷酸化激活c-Jun氨基末端激酶:一种由热休克蛋白72(HSP72)控制的新途径。
Mol Cell Biol. 1999 Apr;19(4):2547-55. doi: 10.1128/MCB.19.4.2547.
10
Protein prenylation: molecular mechanisms and functional consequences.蛋白质异戊二烯化:分子机制与功能后果
Annu Rev Biochem. 1996;65:241-69. doi: 10.1146/annurev.bi.65.070196.001325.

细胞穿透性异戊烯化肽的序列和长度依赖性研究。

Investigation of the sequence and length dependence for cell-penetrating prenylated peptides.

机构信息

Department of Chemistry, University of Minnesota, 207 Pleasant Street SE, Minneapolis, MN 55455, USA.

出版信息

Bioorg Med Chem Lett. 2010 Jan 1;20(1):161-3. doi: 10.1016/j.bmcl.2009.11.026. Epub 2009 Nov 13.

DOI:10.1016/j.bmcl.2009.11.026
PMID:20004573
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2834556/
Abstract

Cell penetrating peptides are useful delivery tools for introducing molecules of interest into cells. A new class of cell penetrating molecules has been recently reported-cell penetrating, prenylated peptides. In this study a series of such peptides was synthesized to examine the relationship between peptide sequence and level of peptide internalization and to probe their mechanism of internalization. This study revealed that prenylated peptides internalize via a non-endocytotic pathway regardless of sequence. Sequence length and identity was found to play a role in peptide uptake but prenylated sequences as short as two amino acids were found to exhibit significant cell penetrating properties.

摘要

细胞穿透肽是将感兴趣的分子导入细胞的有用的传递工具。最近报道了一类新的细胞穿透分子 - 细胞穿透, prenylated 肽。在这项研究中,合成了一系列这样的肽,以研究肽序列与肽内化水平之间的关系,并探究其内化机制。本研究表明,prenylated 肽通过非胞吞途径内化,与序列无关。序列长度和同一性被发现对肽摄取起作用,但发现短至两个氨基酸的 prenylated 序列表现出显著的细胞穿透特性。