Mechanisms of cellular uptake of cell-penetrating peptides.

Fatemeh Madani, Staffan Lindberg, Ulo Langel, Shiroh Futaki, Astrid Gräslund
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引用次数: 843

Abstract

Recently, much attention has been given to the problem of drug delivery through the cell-membrane in order to treat and manage several diseases. The discovery of cell penetrating peptides (CPPs) represents a major breakthrough for the transport of large-cargo molecules that may be useful in clinical applications. CPPs are rich in basic amino acids such as arginine and lysine and are able to translocate over membranes and gain access to the cell interior. They can deliver large-cargo molecules, such as oligonucleotides, into cells. Endocytosis and direct penetration have been suggested as the two major uptake mechanisms, a subject still under debate. Unresolved questions include the detailed molecular uptake mechanism(s), reasons for cell toxicity, and the delivery efficiency of CPPs for different cargoes. Here, we give a review focused on uptake mechanisms used by CPPs for membrane translocation and certain experimental factors that affect the mechanism(s).

Abstract Image

穿透细胞肽的细胞摄取机制。
近年来,为了治疗和控制多种疾病,药物通过细胞膜传递的问题受到了广泛的关注。细胞穿透肽(CPPs)的发现代表了大货物分子运输的重大突破,可能在临床应用中有用。CPPs富含基本氨基酸,如精氨酸和赖氨酸,能够在膜上转运并进入细胞内部。它们可以将诸如寡核苷酸之类的大分子运送到细胞中。内吞作用和直接渗透被认为是两种主要的摄取机制,这一主题仍在争论中。尚未解决的问题包括详细的分子摄取机制、细胞毒性的原因以及CPPs对不同货物的递送效率。在这里,我们重点综述了CPPs用于膜易位的摄取机制以及影响该机制的某些实验因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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