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蛋白包覆的氧化石墨烯纳米片的尺寸依赖性细胞摄取。

Size-dependent cell uptake of protein-coated graphene oxide nanosheets.

机构信息

Department of Chemical Biology & Therapeutics, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, United States.

出版信息

ACS Appl Mater Interfaces. 2012 Apr;4(4):2259-66. doi: 10.1021/am300253c. Epub 2012 Mar 23.

Abstract

As an emerging applied material, graphene has shown tremendous application potential in many fields, including biomedicine. However, the biological behavior of these nanosheets, especially their interactions with cells, is not well understood. Here, we report our findings about the cell surface adhesion, subcellular locations, and size-dependent uptake mechanisms of protein-coated graphene oxide nanosheets (PCGO). Small nanosheets enter cells mainly through clathrin-mediated endocytosis, and the increase of graphene size enhances phagocytotic uptake of the nanosheets. These findings will facilitate biomedical and toxicologic studies of graphenes and provide fundamental understanding of interactions at the interface of two-dimensional nanostructures and biological systems.

摘要

作为一种新兴的应用材料,石墨烯在许多领域,包括生物医药领域,显示出了巨大的应用潜力。然而,这些纳米片的生物学行为,特别是它们与细胞的相互作用,还不是很清楚。在这里,我们报告了我们关于蛋白包覆的氧化石墨烯纳米片(PCGO)的细胞表面黏附、亚细胞定位和尺寸依赖性摄取机制的研究结果。小的纳米片主要通过网格蛋白介导的内吞作用进入细胞,而石墨烯尺寸的增加增强了纳米片的吞噬摄取。这些发现将促进对石墨烯的生物医学和毒理学研究,并为二维纳米结构与生物系统界面相互作用提供基本的理解。

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