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Time-resolved Proteomic Visualization of Dendrimer Cellular Entry and Trafficking

机译:树状大分子细胞进入和贩运的时间分辨蛋白质组学可视化。

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摘要

Our understanding of the complex cell entry pathways would greatly benefit from a comprehensive characterization of key proteins involved in this dynamic process. Here we devise a novel proteomic strategy named TITAN (Tracing Internalization and TrAfficking of Nanomaterials) to reveal real-time protein-dendrimer interactions using a systems biology approach. Dendrimers functionalized with photoreactive crosslinkers were internalized by HeLa cells and irradiated at set time intervals, then isolated and subjected to quantitative proteomics. In total, 809 interacting proteins crosslinked with dendrimers were determined by TITAN in a detailed temporal manner during dendrimer internalization, traceable to at least two major endocytic mechanisms, clathrin-mediated and caveolar/raft-mediated endocytosis. The direct involvement of the two pathways was further established by the inhibitory effect of dynasore on dendrimer uptake and changes in temporal profiles of key proteins.
机译:我们对复杂细胞进入途径的理解将大大受益于此动态过程中涉及的关键蛋白质的全面表征。在这里,我们设计了一种新的蛋白质组学策略,称为TITAN(纳米材料的追踪内化和交易),以使用系统生物学方法揭示实时蛋白质-树状大分子相互作用。用光反应性交联剂官能化的树状聚合物被HeLa细胞内化并以设定的时间间隔照射,然后分离并进行定量蛋白质组学分析。在树状大分子内化过程中,TITAN以详细的时间方式总共确定了809个与树状大分子交联的相互作用蛋白,可追溯到至少两种主要的内吞机制,网格蛋白介导的和胞浆/筏介导的内吞作用。 dynasore对树状大分子摄取的抑制作用和关键蛋白质的时间变化,进一步确立了这两种途径的直接参与。

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