Cell-Penetrating Peptide-Mediated Biomolecule Transportation in Artificial Lipid Vesicles and Living Cells

被引:4
作者
Miwa, Akari [1 ]
Kamiya, Koki [1 ]
机构
[1] Gunma Univ, Grad Sch Sci & Technol, Div Mol Sci, Kiryu, Gunma 3768515, Japan
来源
MOLECULES | 2024年 / 29卷 / 14期
基金
日本学术振兴会;
关键词
membrane-active peptide; cell-penetrating peptide; lipid vesicle; artificial cell model; biomolecule transport; protein transport; therapy; ARGININE-RICH PEPTIDES; INTRACELLULAR DELIVERY; IN-VIVO; SECONDARY STRUCTURE; ENDOSOMAL ESCAPE; MOLECULAR-MECHANISMS; MEMBRANE INTERACTION; PHOSPHATASE CASCADE; PROTEIN-TRANSPORT; PLASMA-MEMBRANE;
D O I
10.3390/molecules29143339
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
Signal transduction and homeostasis are regulated by complex protein interactions in the intracellular environment. Therefore, the transportation of impermeable macromolecules (nucleic acids, proteins, and drugs) that control protein interactions is essential for modulating cell functions and therapeutic applications. However, macromolecule transportation across the cell membrane is not easy because the cell membrane separates the intra/extracellular environments, and the types of molecular transportation are regulated by membrane proteins. Cell-penetrating peptides (CPPs) are expected to be carriers for molecular transport. CPPs can transport macromolecules into cells through endocytosis and direct translocation. The transport mechanism remains largely unclear owing to several possibilities. In this review, we describe the methods for investigating CPP conformation, translocation, and cargo transportation using artificial membranes. We also investigated biomolecular transport across living cell membranes via CPPs. Subsequently, we show not only the biochemical applications but also the synthetic biological applications of CPPs. Finally, recent progress in biomolecule and nanoparticle transportation via CPPs into specific tissues is described from the viewpoint of drug delivery. This review provides the opportunity to discuss the mechanism of biomolecule transportation through these two platforms.
引用
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页数:21
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