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细胞穿透肽与棒状生物纳米粒子的整合:受病毒启发的基因沉默技术。

Integration of Cell-Penetrating Peptides with Rod-like Bionanoparticles: Virus-Inspired Gene-Silencing Technology.

机构信息

Key Laboratory of Photochemical Conversion and Optoelectronic Materials , Technical Institute of Physics and Chemistry, Chinese Academy of Sciences , 29 Zhongguancun East Road , Beijing 100190 , P. R. China.

CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety , Institute of High Energy Physics, Chinese Academy of Sciences , No. 19(B) Yuquan Road , Beijing 100049 , P. R. China.

出版信息

Nano Lett. 2018 Sep 12;18(9):5453-5460. doi: 10.1021/acs.nanolett.8b01805. Epub 2018 Aug 13.

DOI:10.1021/acs.nanolett.8b01805
PMID:30091612
Abstract

Inspired by the high gene transfer efficiency of viral vectors and to avoid side effects, we present here a 1D rod-like gene-silencing vector based on a plant virus. By decorating the transacting activator of transduction (TAT) peptide on the exterior surface, the TAT-modified tobacco mosaic virus (TMV) achieves a tunable isoelectric point (from ∼3.5 to ∼9.6) depending on the TAT dose. In addition to enhanced cell internalization, this plant virus-based vector (TMV-TAT) acquired endo/lysosomal escape capacity without inducing lysosomal damage, resulting in both high efficiency and low cytotoxicity. By loading silencer green fluorescent protein (GFP) siRNA onto the TMV-TAT vector (siRNA@TMV-TAT) and interfering with GFP-expressing mouse epidermal stem cells (ESCs/GFP) in vitro, the proportion of GFP-positive cells could be knocked down to levels even lower than 15% at a concentration of ∼100% cell viability. Moreover, by interfering with GFP-expressing highly metastatic hepatocellular carcinoma (MHCC97-H/GFP) tumors in vivo, treatment with siRNA@TMV-TAT complexes for 10 days achieved a GFP-negative rate as high as 80.8%. This work combines the high efficiency of viral vectors and the safety of nonviral vectors and may provide a promising strategy for gene-silencing technology.

摘要

受病毒载体高基因转移效率的启发,并为避免副作用,我们在此提出了一种基于植物病毒的 1D 棒状基因沉默载体。通过在转导激活因子(TAT)肽的外表面进行修饰,TAT 修饰的烟草花叶病毒(TMV)可以根据 TAT 剂量实现可调等电点(从∼3.5 到∼9.6)。除了增强细胞内化外,这种基于植物病毒的载体(TMV-TAT)还获得了内体/溶酶体逃逸能力,而不会诱导溶酶体损伤,从而实现了高效率和低细胞毒性。通过将沉默绿色荧光蛋白(GFP)siRNA 加载到 TMV-TAT 载体上(siRNA@TMV-TAT),并干扰体外表达 GFP 的小鼠表皮干细胞(ESCs/GFP),GFP 阳性细胞的比例可以降低到甚至低于 15%,而细胞活力仍保持在约 100%。此外,通过干扰体内表达 GFP 的高转移性肝癌(MHCC97-H/GFP)肿瘤,用 siRNA@TMV-TAT 复合物治疗 10 天,GFP 阴性率高达 80.8%。这项工作结合了病毒载体的高效率和非病毒载体的安全性,可能为基因沉默技术提供了一种有前途的策略。

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