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Continuous spectroscopic measurements of photo-stimulated release of molecules by nanomachines in a single living cell

机译:连续光谱的测量photo-stimulated释放的分子纳米机器在一个活细胞

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摘要

The first continuous, real-time spectroscopic monitoring of a photo-driven cargo delivery event from a mesoporous silica-based nanocarrier inside a single living cell is reported. By chemically attaching azobenzene molecules inside the 3 nm pore channels of mesoporous silica nanoparticles (~70 nm diameter), the escape of the cargo molecule [propidium iodide (PI)] from the pore is prevented in the dark but is facilitated by the light-driven isomerization motion. Real-time spectroscopic measurements of a single cell uncover intermediate processes that occur during this intracellular delivery event, from nanomachine activation to the release of PI into the cytosol and to PI's eventual intercalation with nuclear DNA. Changes in PI's fluorescence intensity and the hypsochromic shift of the band maxima are used to identify the local environment of the fluorophore that is being observed in the cell. The ability to precisely initiate a chemical event inside an individual cell and continuously monitor the subsequent biological responses will enhance our understanding of intracellular process upon drug, protein and nucleic acid delivery.
机译:第一个连续、实时光谱监测主要以照片呈现的货物交付以事件从介孔硅基nanocarrier里面一个活细胞。将偶氮苯分子在3海里介孔二氧化硅纳米粒子的孔隙通道(~ 70 nm直径),逃脱的货物分子(propidium碘(π)]的孔隙避免在黑暗中,但提供了便利light-driven异构化运动。一个细胞的光谱测量结果发现中间过程时产生的这种细胞内交付事件,从nanomachine激活释放π胞质和π的最终夹层核DNA。强度和乐队的蓝移maxima是用来确定当地环境所观察到的荧光团细胞。在单个细胞和化学事件持续监测随后的生物将提高我们理解的反应细胞内的过程在药物、蛋白质和核酸交付。

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