Tashima Toshihiko
Tashima Laboratories of Arts and Sciences, 1239-5 Toriyama-cho, Kohoku-ku, Yokohama, Kanagawa 222-0035, Japan.
Bioorg Med Chem Lett. 2017 Jan 15;27(2):121-130. doi: 10.1016/j.bmcl.2016.11.083. Epub 2016 Nov 30.
Cell-penetrating peptides (CPPs) are oligopeptides that can permeate the cell membrane. The use of a CPP-mediated transport system could be an excellent method for delivering cell-impermeable substances such as proteins, antibodies, antisense oligonucleotides, siRNAs, plasmids, drugs, fluorescent compounds, and nanoparticles as covalently or noncovalently conjugated cargo into cells. Nonetheless, the mechanisms through which CPPs are internalized remain unclear. Endocytosis and direct translocation through the membrane are the generally accepted routes. Internalization via both pathways can occur simultaneously, depending on cellular conditions. However, the peculiar property of CPPs has attracted many researchers, especially in drug discovery or development, who intend to deliver impermeable substances into cells through the cell membrane. The delivery of drugs using CPPs may non-invasively solve the problem of drug penetration into cells with the added benefit of low cytotoxicity. Moreover, macromolecules can also be delivered by this transport system. In this review, I discuss the possibilities and advantages of substance delivery into cells using CPPs.
细胞穿透肽(CPPs)是能够穿透细胞膜的寡肽。使用CPP介导的转运系统可能是一种将蛋白质、抗体、反义寡核苷酸、小干扰RNA、质粒、药物、荧光化合物和纳米颗粒等不能透过细胞的物质作为共价或非共价结合的货物递送至细胞内的极佳方法。尽管如此,CPPs内化的机制仍不清楚。内吞作用和通过膜的直接转运是普遍接受的途径。根据细胞条件,两种途径的内化可以同时发生。然而,CPPs的独特性质吸引了许多研究人员,特别是在药物发现或开发领域,他们希望通过细胞膜将不能透过细胞的物质递送至细胞内。使用CPPs递送药物可能以低细胞毒性这一额外优势无创地解决药物渗透进入细胞的问题。此外,大分子也可以通过这种转运系统递送。在这篇综述中,我将讨论使用CPPs将物质递送至细胞内的可能性和优势。