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用于增强核酸递送的细胞穿透肽偶联壳聚糖

Cell Penetrating Peptide Conjugated Chitosan for Enhanced Delivery of Nucleic Acid.

作者信息

Layek Buddhadev, Lipp Lindsey, Singh Jagdish

机构信息

Department of Pharmaceutics, College of Pharmacy, University of Minnesota, 308 Harvard Street S.E., Minneapolis, MN 55455, USA.

Department of Pharmaceutical Sciences, School of Pharmacy, North Dakota State University, Fargo, ND 58105, USA.

出版信息

Int J Mol Sci. 2015 Dec 4;16(12):28912-30. doi: 10.3390/ijms161226142.

Abstract

Gene therapy is an emerging therapeutic strategy for the cure or treatment of a spectrum of genetic disorders. Nevertheless, advances in gene therapy are immensely reliant upon design of an efficient gene carrier that can deliver genetic cargoes into the desired cell populations. Among various nonviral gene delivery systems, chitosan-based carriers have gained increasing attention because of their high cationic charge density, excellent biocompatibility, nearly nonexistent cytotoxicity, negligible immune response, and ideal ability to undergo chemical conjugation. However, a major shortcoming of chitosan-based carriers is their poor cellular uptake, leading to inadequate transfection efficiency. The intrinsic feature of cell penetrating peptides (CPPs) for transporting diverse cargoes into multiple cell and tissue types in a safe manner suggests that they can be conjugated to chitosan for improving its transfection efficiency. In this review, we briefly discuss CPPs and their classification, and also the major mechanisms contributing to the cellular uptake of CPPs and cargo conjugates. We also discuss immense improvements for the delivery of nucleic acids using CPP-conjugated chitosan-based carriers with special emphasis on plasmid DNA and small interfering RNA.

摘要

基因治疗是一种新兴的治疗策略,用于治愈或治疗一系列遗传疾病。然而,基因治疗的进展在很大程度上依赖于高效基因载体的设计,这种载体能够将遗传物质传递到所需的细胞群体中。在各种非病毒基因递送系统中,基于壳聚糖的载体因其高阳离子电荷密度、优异的生物相容性、几乎不存在的细胞毒性、可忽略不计的免疫反应以及进行化学偶联的理想能力而受到越来越多的关注。然而,基于壳聚糖的载体的一个主要缺点是其细胞摄取能力差,导致转染效率不足。细胞穿透肽(CPPs)能够以安全的方式将多种物质运输到多种细胞和组织类型中,这一内在特性表明它们可以与壳聚糖偶联以提高其转染效率。在这篇综述中,我们简要讨论了细胞穿透肽及其分类,以及促成细胞穿透肽和货物偶联物细胞摄取的主要机制。我们还讨论了使用与细胞穿透肽偶联的基于壳聚糖的载体递送核酸方面的巨大改进,特别强调了质粒DNA和小干扰RNA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4376/4691089/ab72258f039e/ijms-16-26142-g001.jpg

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