Erazo-Oliveras Alfredo, Muthukrishnan Nandhini, Baker Ryan, Wang Ting-Yi, Pellois Jean-Philippe
Department of Biochemistry and Biophysics, Texas A&M University, Room 430, 300 Olsen Blvd., College Station, TX 77843-2128, USA.
Pharmaceuticals (Basel). 2012 Nov 1;5(11):1177-1209. doi: 10.3390/ph5111177.
Cell penetrating peptides (CPPs) can deliver cell-impermeable therapeutic cargos into cells. In particular, CPP-cargo conjugates tend to accumulate inside cells by endocytosis. However, they often remain trapped inside endocytic organelles and fail to reach the cytosolic space of cells efficiently. In this review, the evidence for CPP-mediated endosomal escape is discussed. In addition, several strategies that have been utilized to enhance the endosomal escape of CPP-cargos are described. The recent development of branched systems that display multiple copies of a CPP is presented. The use of viral or synthetic peptides that can disrupt the endosomal membrane upon activation by the low pH of endosomes is also discussed. Finally, we survey how CPPs labeled with chromophores can be used in combination with light to stimulate endosomal lysis. The mechanisms and challenges associated with these intracellular delivery methodologies are discussed.
细胞穿透肽(CPPs)能够将细胞不可渗透的治疗性货物递送至细胞内。特别地,CPP-货物缀合物倾向于通过内吞作用在细胞内积累。然而,它们常常被困在内吞细胞器内,无法有效地到达细胞的胞质空间。在这篇综述中,讨论了CPP介导的内体逃逸的证据。此外,还描述了几种用于增强CPP-货物内体逃逸的策略。介绍了展示多个CPP拷贝的分支系统的最新进展。还讨论了使用可在内体低pH激活时破坏内体膜的病毒或合成肽。最后,我们探讨了用发色团标记的CPP如何与光结合使用以刺激内体裂解。讨论了与这些细胞内递送方法相关的机制和挑战。