School of Applied Sciences, Royal Melbourne Institute of Technology, Bundoora, Victoria, Australia.
J Pept Sci. 2012 Aug;18(8):527-34. doi: 10.1002/psc.2430. Epub 2012 Jul 4.
There is considerable interest in the sub-cellular targeting and delivery of biomolecules, therapeutic and imaging agents, and nanoparticles and nanoparticle conjugates into organelles for therapeutic and imaging purposes. To date, a number of studies have used sorting peptides for targeted delivery of cargo into different cell organelles but not into lysosomes. In this study, the delivery of 13-nm gold nanoparticles across the cell membrane followed by targeted localisation into the lysosomes of a mammalian cell line was examined using novel combinations of cell-penetrating peptides and lysosomal sorting peptides conjugated to the nanoparticles. Using a combination of fluorescence spectroscopy, fluorescence microscopy and transmission electron microscopy techniques, we show that these nanoconjugates were efficiently and selectively delivered into the lysosomes with minimal cytotoxic effects. This novel targeted delivery system may underpin the development of a new strategy for the treatment of lysosomal storage diseases by exploiting the large surface area of nanoparticles to deliver drugs or replacement enzymes directly to the lysosomes.
人们对生物分子、治疗剂和成像剂以及纳米颗粒和纳米颗粒缀合物的亚细胞靶向和递送至细胞器(用于治疗和成像目的)非常感兴趣。迄今为止,许多研究已经使用分拣肽将货物靶向递送至不同的细胞细胞器,但不能递送至溶酶体。在这项研究中,使用新型细胞穿透肽和溶酶体分拣肽与纳米颗粒的组合,研究了穿过细胞膜的 13nm 金纳米颗粒的递送至哺乳动物细胞系的溶酶体中的靶向定位。通过荧光光谱法、荧光显微镜和透射电子显微镜技术的组合,我们表明这些纳米缀合物能够高效且选择性地递送至溶酶体,同时具有最小的细胞毒性作用。这种新型靶向递送系统可能为利用纳米颗粒的大表面积将药物或替代酶直接递送至溶酶体来治疗溶酶体贮积病提供一种新的策略。