Suppr超能文献

由细胞穿透肽和无毒聚合物组成的基因递送系统的开发。

Development of a Gene Delivery System Composed of a Cell-Penetrating Peptide and a Nontoxic Polymer.

作者信息

Covarrubias-Zambrano Obdulia, Shrestha Tej B, Pyle Marla, Montes-Gonzalez Maria, Troyer Deryl L, Bossmann Stefan H

机构信息

Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, United States.

Nanotechnology Innovation Center of Kansas State, Kansas State University, Manhattan, Kansas 66506, United States.

出版信息

ACS Appl Bio Mater. 2020 Nov 16;3(11):7418-7427. doi: 10.1021/acsabm.0c00561. Epub 2020 Oct 16.

Abstract

Major concerns have arisen with respect to using viral vectors for gene therapies. Collateral effects include cancer resistance, development of new cancers, and even systemic deaths. For this reason, researchers have focused on the alternative of using nonviral nanocarriers for gene therapy. In this study, a gene delivery nanocarrier was developed, comprising a cell-penetrating peptide called WTAS as a primary nanocarrier and a poly(β-amino ester) (PBAE) polymer as a secondary nanocarrier. Here, the PBAE polymer is used to protect the WTAS peptide from early degradation while further facilitating the transportation into cells. WTAS is a peptide that penetrates cell nuclei within a few minutes after exposure, which makes it an ideal candidate to transport genetic materials. The PBAE-WTAS nanocarrier was assembled and tested against three cell lines (NSC, B16F10, and GL26). Cytotoxic studies demonstrated the relatively low toxicity of the PBAE-WTAS nanocarrier and PBAE-WTAS loaded with green fluorescent protein (GFP) plasmid DNA (pDNA@PBAE-WTAS) against all three cell lines. Cell transfection experiments were carried out using GL26 cells. These studies demonstrated a very high transfection rate of PBAE-WTAS loaded with GFP plasmid DNA, leading to virtually complete transfection (> 90%). In conclusion, we report a very promising gene delivery nanocarrier, which can be further modified to transport a variety of genetic materials for targeted therapy of multiple diseases.

摘要

关于将病毒载体用于基因治疗已经出现了重大问题。附带效应包括抗癌性、新癌症的发生,甚至全身性死亡。因此,研究人员将重点转向使用非病毒纳米载体进行基因治疗的替代方法。在本研究中,开发了一种基因递送纳米载体,其包含一种名为WTAS的细胞穿透肽作为主要纳米载体和一种聚(β-氨基酯)(PBAE)聚合物作为次要纳米载体。在此,PBAE聚合物用于保护WTAS肽免于早期降解,同时进一步促进其进入细胞的运输。WTAS是一种在暴露后几分钟内就能穿透细胞核的肽,这使其成为运输遗传物质的理想候选者。组装了PBAE-WTAS纳米载体并针对三种细胞系(NSC、B16F10和GL26)进行了测试。细胞毒性研究表明,PBAE-WTAS纳米载体和负载绿色荧光蛋白(GFP)质粒DNA的PBAE-WTAS(pDNA@PBAE-WTAS)对所有三种细胞系的毒性相对较低。使用GL26细胞进行了细胞转染实验。这些研究表明,负载GFP质粒DNA的PBAE-WTAS具有非常高的转染率,几乎导致完全转染(>90%)。总之,我们报道了一种非常有前景的基因递送纳米载体,其可以进一步修饰以运输多种遗传物质用于多种疾病的靶向治疗。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验