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In what time scale proton transfer takes place in a live CHO cell?

机译:质子转移在什么时间在活的CHO细胞中进行?

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Excited state proton transfer (ESPT) of pyranine (8-hydroxypyrene-1,3,6- trisulfonate, HPTS) in a live Chinese hamster ovary (CHO) cell is studied by time resolved confocal microscopy. The cytoplasm region of the cell is stained by a photoacid, HPTS (HA). The time constant of initial proton transfer (τ_(PT)) in the cell is found to be ~10 times longer than that in bulk water, while the time constants of recombination (τ_(rec)) and dissociation (τ_(diss)) in the cell are ~3 times and ~2 times longer, respectively. The slower rate of proton transfer (~10 times) inside the CHO cell compared to that in bulk water is ascribed to slower solvation dynamics, lower availability of free water molecules, and disruption of hydrogen-bond network inside the cell. Translational and rotational diffusion of HPTS inside a single CHO cell have been investigated by fluorescence correlation spectroscopy (FCS) and picosecond anisotropy measurement, respectively. Both the translational and rotational diffusion slow down inside the live cell. FCS studies indicate that HPTS remains tightly bound to a macromolecule inside the cell.
机译:通过时间分辨共聚焦显微镜研究了吡喃(8-羟基CHO-1,3,6-三磺酸盐,HPTS)在活的中国仓鼠卵巢(CHO)细胞中的兴奋态质子转移(ESPT)。细胞的细胞质区域被光酸HPTS(HA)染色。发现单元中初始质子转移的时间常数(τ_(PT))比散装水中的时间常数长约10倍,而重组(τ_(rec))和解离(τ_(diss))的时间常数单元中的时间分别是〜3倍和〜2倍。与大量水中相比,CHO细胞内部质子转移速率较低(约10倍),这归因于较慢的溶剂化动力学,较低的自由水分子可利用性以及细胞内氢键网络的破坏。分别通过荧光相关光谱法(FCS)和皮秒各向异性测量研究了单个CHO细胞内HPTS的平移和旋转扩散。平移和旋转扩散都在活细胞内部减慢。 FCS研究表明,HPTS仍然与细胞内的大分子紧密结合。

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