Cell-Penetrating Peptides Escape the Endosome by Inducing Vesicle Budding and Collapse

被引:67
作者
Sahni, Ashweta [1 ]
Qian, Ziqing [1 ]
Pei, Dehua [1 ]
机构
[1] Ohio State Univ, Dept Chem & Biochem, Columbus, OH 43210 USA
基金
美国国家卫生研究院;
关键词
ARGININE-RICH PEPTIDES; TAT-FUSION PROTEINS; EFFICIENT DELIVERY; PLASMA-MEMBRANE; TRANSLOCATION; ENDOCYTOSIS; INTERNALIZATION; VIRUSES;
D O I
10.1021/acschembio.0c00478
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cell-penetrating peptides (CPPs) are capable of delivering membrane-impermeable cargoes (including small molecules, peptides, proteins, nucleic acids, and nanoparticles) into the cytosol of mammalian cells and have the potential to revolutionize biomedical research and drug discovery. However, the mechanism of action of CPPs has remained poorly understood, especially how they escape from the endosome into the cytosol following endocytic uptake. We show herein that CPPs exit the endosome by inducing budding and collapse of CPP-enriched vesicles from the endosomal membrane. This mechanism provides a theoretical basis for designing CPPs and other delivery vehicles of improved efficiencies.
引用
收藏
页码:2485 / 2492
页数:8
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