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用于脂质体细胞内递送的受限和紫外激活的细胞穿透肽。

Constrained and UV-activatable cell-penetrating peptides for intracellular delivery of liposomes.

机构信息

Radboud University Nijmegen, Institute for Molecules and Materials, Department of Organic Chemistry, Heyendaalseweg 135, 6525 AJ Nijmegen, The Netherlands.

出版信息

J Control Release. 2012 Nov 28;164(1):87-94. doi: 10.1016/j.jconrel.2012.10.008. Epub 2012 Oct 17.

Abstract

Herein we report on the development of a novel method of constraining a cell-penetrating peptide, which can be used to trigger transport of liposomes into cells upon in this case radiation with UV-light. A cell-penetrating peptide, which was modified on both termini with an alkyl chain, was anchored to the liposomal surface in a constrained and deactivated form. Since one of the two alkyl chains was connected to the peptide via a UV-cleavable linker, disconnection of this alkyl chain upon irradiation led to the exposure of the cell-penetrating peptide, and mediated the transport of the entire liposome particle into cells.

摘要

在此,我们报告了一种新的限制细胞穿透肽的方法的发展,该方法可用于在这种情况下通过紫外线辐射触发脂质体进入细胞的运输。一种在两端都用烷基链修饰的细胞穿透肽以受约束和失活的形式锚定在脂质体表面上。由于两个烷基链中的一个通过紫外线可裂解的连接子连接到肽上,因此照射后该烷基链的断开导致细胞穿透肽的暴露,并介导整个脂质体颗粒进入细胞。

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