Morales Demosthenes P, Braun Gary B, Pallaoro Alessia, Chen Renwei, Huang Xiao, Zasadzinski Joseph A, Reich Norbert O
Department of Chemistry and Biochemistry, University of California , Santa Barbara, California 93106, United States.
Mol Pharm. 2015 Feb 2;12(2):600-9. doi: 10.1021/mp500675p. Epub 2014 Dec 23.
While a host of methods exist to deliver genetic materials or small molecules to cells, very few are available for protein delivery to the cytosol. We describe a modular, light-activated nanocarrier that transports proteins into cells by receptor-mediated endocytosis and delivers the cargo to the cytosol by light triggered endosomal escape. The platform is based on hollow gold nanoshells (HGN) with polyhistidine tagged proteins attached through an avidity-enhanced, nickel chelation linking layer; here, we used green fluorescent protein (GFP) as a model deliverable cargo. Endosomal uptake of the GFP loaded nanocarrier was mediated by a C-end Rule (CendR) internalizing peptide fused to the GFP. Focused femtosecond pulsed-laser excitation triggered protein release from the nanocarrier and endosome disruption, and the released protein was capable of targeting the nucleoli, a model intracellular organelle. We further demonstrate the generality of the approach by loading and releasing Sox2 and p53. This method for targeting of individual cells, with resolution similar to microinjection, provides spatial and temporal control over protein delivery.
虽然存在许多将遗传物质或小分子递送至细胞的方法,但可用于将蛋白质递送至细胞质的方法却很少。我们描述了一种模块化的光激活纳米载体,它通过受体介导的内吞作用将蛋白质转运到细胞中,并通过光触发的内体逃逸将货物递送至细胞质。该平台基于中空金纳米壳(HGN),通过亲和力增强的镍螯合连接层连接多组氨酸标记的蛋白质;在这里,我们使用绿色荧光蛋白(GFP)作为可递送货物的模型。负载GFP的纳米载体的内体摄取由与GFP融合的C端规则(CendR)内化肽介导。聚焦飞秒脉冲激光激发触发纳米载体释放蛋白质并破坏内体,释放的蛋白质能够靶向核仁,这是一种细胞内细胞器模型。我们通过加载和释放Sox2和p53进一步证明了该方法的通用性。这种靶向单个细胞的方法,分辨率类似于显微注射,可提供对蛋白质递送的空间和时间控制。