核酸
内体
细胞内
内吞作用
化学
基因传递
生物物理学
共价键
纳米颗粒
细胞膜
生物化学
细胞
细胞生物学
转染
基因
生物
有机化学
作者
Piret Arukuusk,Ly Pärnaste,Mattias Hällbrink,Ülo Langel
出处
期刊:Methods in molecular biology
日期:2015-01-01
卷期号:: 303-315
被引量:30
标识
DOI:10.1007/978-1-4939-2806-4_19
摘要
Nucleic acids can be utilized in gene therapy to restore, alter, or silence gene functions. In order to reveal the biological activity nucleic acids have to reach their intracellular targets by passing through the plasma membrane, which is impermeable for these large and negatively charged molecules. Cell-penetrating peptides (CPPs) condense nucleic acids into nanoparticles using non-covalent complexation strategy and mediate their delivery into the cell, whereas the physicochemical parameters of the nanoparticles determine the interactions with the membranes, uptake mechanism, and subsequent intracellular fate. The nanoparticles are mostly internalized by endocytosis that leads to the entrapment of them in endosomal vesicles. Therefore design of new CPPs that are applicable for non-covalent complex formation strategy and harness endosomolytic properties is highly vital. Here we demonstrate that PepFects and NickFects are efficient vectors for the intracellular delivery of various nucleic acids.This chapter describes how to form CPP/pDNA nanoparticles, evaluate stable nanoparticles formation, and assess gene delivery efficacy.
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