Department of Biochemistry and Biophysics, The Arrhenius Laboratories for Natural Sciences, Stockholm University, Svante Arrhenius väg 16B, SE-10691 Stockholm, Sweden.
J Mater Chem B. 2020 Dec 21;8(47):10825-10836. doi: 10.1039/d0tb01106a. Epub 2020 Nov 11.
Cell-penetrating peptides are a promising therapeutic strategy for a wide variety of degenerative diseases, ageing, and cancer. Among the multitude of cell-penetrating peptides, PepFect14 has been preferentially used in our laboratory for oligonucleotide delivery into cells and in vivo mouse models. However, this activity has mainly been reported towards cytoplasm and nuclei, while the mentioned disorders have been linked to mitochondrial defects. Here, we report a library generated from a combinatorial covalent fusion of a mitochondrial-penetrating peptide, mtCPP1, and PepFect14 in order to deliver therapeutic biomolecules to influence mitochondrial protein expression. The non-covalent complexation of these peptides with oligonucleotides resulted in nano-complexes affecting biological functions in the cytoplasm and on mitochondria. This delivery system proved to efficiently target mitochondrial genes, providing a framework for the development of mitochondrial peptide-based oligonucleotide technologies with the potential to be used as a treatment for patients with mitochondrial disorders.
细胞穿透肽是治疗多种退行性疾病、衰老和癌症的有前途的治疗策略。在众多细胞穿透肽中,PepFect14 已被优先用于我们实验室将寡核苷酸递送至细胞和体内小鼠模型中。然而,这种活性主要是针对细胞质和细胞核报告的,而上述疾病与线粒体缺陷有关。在这里,我们报告了一个从线粒体穿透肽 mtCPP1 和 PepFect14 的组合共价融合生成的文库,以便将治疗性生物分子递送至影响线粒体蛋白表达的位置。这些肽与寡核苷酸的非共价复合导致纳米复合物影响细胞质和线粒体中的生物学功能。该递送系统被证明能够有效地靶向线粒体基因,为开发基于线粒体肽的寡核苷酸技术提供了框架,这些技术有可能被用作治疗线粒体疾病患者的方法。