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通过疏水相互作用稳定癌症特异性基因载体,以清晰响应癌症信号。

Stabilization of cancer-specific gene carrier via hydrophobic interaction for a clear-cut response to cancer signaling.

机构信息

Graduate School of Systems Life Sciences, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan.

出版信息

J Control Release. 2013 Sep 28;170(3):469-76. doi: 10.1016/j.jconrel.2013.06.011. Epub 2013 Jun 18.

Abstract

Here, we developed a new gene carrier, comprising a linear polyethylenimine (LPEI) grafted with a hydrophobically modified cationic peptide containing a long alkyl chain, for use in cancer-specific gene delivery. The cationic peptide is a substrate of protein kinase Cα (PKCα), which is known to be activated specifically in cancer cells. The hydrophobically modified LPEI-peptide conjugate (LPEI-C10-peptide) could form a polyplex with DNA through electrostatic and hydrophobic interactions between the anionic DNA strands and the cationic peptide substrate. The hydrophobic modification of the peptide did not affect the reactivity of the peptide toward PKCα, while the polyplex showed improved intracellular uptake. Because of the efficient endosomal escape and enhanced stability, the polyplex significantly improved the transgene regulation responding to intracellular PKCα activity.

摘要

在这里,我们开发了一种新的基因载体,由线性聚乙烯亚胺(LPEI)与含有长烷基链的疏水改性阳离子肽接枝而成,用于癌症特异性基因传递。该阳离子肽是蛋白激酶 Cα(PKCα)的底物,已知其在癌细胞中特异性激活。疏水性改性的 LPEI-肽缀合物(LPEI-C10-肽)可以通过带负电荷的 DNA 链与阳离子肽底物之间的静电和疏水相互作用与 DNA 形成多聚物。肽的疏水性修饰并不影响肽对 PKCα 的反应性,而多聚物显示出改善的细胞内摄取。由于有效的内涵体逃逸和增强的稳定性,多聚物显著改善了对外源基因表达的调控,以响应细胞内 PKCα 活性。

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