α-Amino acid N-carboxyanhydride (NCA)-derived synthetic polypeptides for nucleic acids delivery

被引:66
|
作者
Liu, Yong [1 ]
Yin, Lichen [1 ]
机构
[1] Soochow Univ, Collaborat Innovat Ctr Suzhou Nano Sci & Technol, Inst Funct Nano & Soft Mat FUNSOM, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
Polypeptide; N-carboxyanhydride; Nucleic acid delivery; Membrane penetration; Secondary structure; Self-assembly; RING-OPENING POLYMERIZATION; CATIONIC HELICAL POLYPEPTIDES; NONVIRAL GENE DELIVERY; MESOPOROUS SILICA NANOPARTICLES; MESSENGER-RNA; POLYPLEX MICELLES; SIRNA DELIVERY; BLOCK-CATIOMER; DNA DELIVERY; IN-VIVO;
D O I
10.1016/j.addr.2020.12.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In recent years, gene therapy has come into the spotlight for the prevention and treatment of a wide range of diseases. Polypeptides have been widely used in mediating nucleic acid delivery, due to their versatilities in chemical structures, desired biodegradability, and low cytotoxicity. Chemistry plays an essential role in the development of innovative polypeptides to address the challenges of producing efficient and safe gene vectors. In this Review, we mainly focused on the latest chemical advances in the design and preparation of polypeptide-based nucleic acid delivery vehicles. We first discussed the synthetic approach of polypeptides via ring-opening polymerization (ROP) of N-carboxyanhydrides (NCAs), and introduced the various types of polypeptide-based gene delivery systems. The extracellular and intracellular barriers against nucleic acid delivery were then outlined, followed by detailed review on the recent advances in polypeptide-based delivery systems that can overcome these barriers to enable in vitro and in vivo gene transfection. Finally, we concluded this review with perspectives in this field. (c) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:139 / 163
页数:25
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