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Targeted Intracellular Delivery of Proteins with Spatial and Temporal Control

机译:蛋白质的靶向细胞内递送,具有时空控制

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摘要

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.
机译:尽管存在许多将遗传物质或小分子传递到细胞的方法,但很少有蛋白质可以传递到细胞质中。我们描述了一种模块化的,光激活的纳米载体,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运送到细胞质中。该平台基于空心金纳米壳(HGN),其具有通过亲和力增强的镍螯合连接层连接的多组氨酸标签蛋白;在这里,我们将绿色荧光蛋白(GFP)用作模型可交付货物。 GFP负载的纳米载体的内体摄取是通过融合到GFP的C末端规则(CendR)内化肽介导的。聚焦的飞秒脉冲激光激发触发了蛋白质从纳米载体的释放和内体破坏,并且释放的蛋白质能够靶向核仁(一种模型细胞内细胞器)。我们通过加载和释放Sox2和p53进一步证明了该方法的一般性。这种靶向单个细胞的方法具有与显微注射相似的分辨率,可提供蛋白质递送的时空控制。

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