Intracellular delivery strategies using membrane-interacting peptides and proteins

被引:0
|
作者
Mai, Linh D. [1 ]
Wimberley, Sydney C. [1 ,2 ]
Champion, Julie A. [1 ,2 ]
机构
[1] Georgia Inst Technol, Sch Chem & Biomol Engn, 950 Atlantic Dr NW, Atlanta, GA 30332 USA
[2] Georgia Inst Technol, Bioengn Program, Atlanta, GA 30332 USA
基金
美国国家卫生研究院;
关键词
CELL-PENETRATING PEPTIDES; IN-VITRO; DRUG; FUSION; NANOPARTICLES; MECHANISMS; INTERNALIZATION; TRANSDUCTION; ENDOCYTOSIS; CHALLENGES;
D O I
10.1039/d4nr02093f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
While the cellular cytosol and organelles contain attractive targets for disease treatments, it remains a challenge to deliver therapeutic biomacromolecules to these sites. This is due to the selective permeability of the plasma and endosomal membranes, especially for large and hydrophilic therapeutic cargos such as proteins and nucleic acids. In response, many different delivery systems and molecules have been devised to help therapeutics cross these barriers to reach cytosolic targets. Among them are peptide and protein-based systems, which have several advantages over other natural and synthetic materials including their ability to interact with cell membranes. In this review, we will describe recent advances and current challenges of peptide and protein strategies that leverage cell membrane association and modulation to enable cytosolic delivery of biomacromolecule cargo. The approaches covered here include peptides and proteins derived from or inspired by natural sequences as well as those designed de novo for delivery function. Cytosolic delivery of therapeutic cargo mediated by membrane interacting peptides and proteins. Created with BioRender.com.
引用
收藏
页码:15465 / 15480
页数:16
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