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Delivery of proteins to mammalian cells via gold nanoparticle mediated laser transfection

机译:通过金纳米粒子介导的激光转染将蛋白质递送至哺乳动物细胞

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摘要

Nanoparticle laser interactions are in widespread use in cell manipulation. In particular, molecular medicine needs techniques for the directed delivery of molecules into mammalian cells. Proteins are the final mediator of most cellular cascades. However, despite several methodical approaches, the efficient delivery of proteins to cells remains challenging. This paper presents a new protein transfection technique via laser scanning of cells previously incubated with gold nanoparticles. The laser-induced plasmonic effects on the gold nanoparticles cause a transient permeabilization of the cellular membrane, allowing proteins to enter the cell. Applying this technique, it was possible to deliver green fluorescent protein into mammalian cells with an efficiency of 43%, maintaining a high level of cell viability. Furthermore, a functional delivery of Caspase 3, an apoptosis mediating protein, was demonstrated and evaluated in several cellular assays. Compared to conventional protein transfection techniques such as microinjection, the methodical approach presented here enables high-throughput transfection of about 10 000 cells per second. Moreover, a well-defined point in time of delivery is guaranteed by gold nanoparticle mediated laser transfection, allowing the detailed temporal analysis of cellular pathways and protein trafficking.
机译:纳米粒子激光相互作用广泛用于细胞操作中。特别地,分子医学需要用于将分子定向递送到哺乳动物细胞中的技术。蛋白质是大多数细胞级联反应的最终介体。然而,尽管采取了几种方法,蛋白质向细胞的有效递送仍然具有挑战性。本文通过激光扫描先前与金纳米颗粒孵育的细胞,提出了一种新的蛋白质转染技术。激光诱导的对金纳米粒子的等离激元效应会引起细胞膜的瞬时透化,从而使蛋白质进入细胞。应用该技术,有可能以43%的效率将绿色荧光蛋白传递到哺乳动物细胞中,并保持高水平的细胞活力。此外,在几种细胞试验中证实并评估了凋亡介导蛋白Caspase 3的功能性传递。与传统的蛋白质转染技术(例如显微注射)相比,此处介绍的方法性方法可实现每秒约10,000个细胞的高通量转染。此外,金纳米粒子介导的激光转染保证了明确的分娩时间,从而可以对细胞途径和蛋白质运输进行详细的时间分析。

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