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Measuring the Viscosity of the Escherichia coli Plasma Membrane Using Molecular Rotors

机译:使用分子转子测量大肠杆菌血浆膜的粘度

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摘要

The viscosity is a highly important parameter within the cell membrane, affecting the diffusion of small molecules and, hence, controlling the rates of intracellular reactions. There is significant interest in the direct, quantitative assessment of membrane viscosity. Here we report the use of fluorescence lifetime imaging microscopy of the molecular rotor BODIPY C10 in the membranes of live Escherichia coli bacteria to permit direct quantification of the viscosity. Using this approach, we investigated the viscosity in live E. coli cells, spheroplasts, and liposomes made from E. coli membrane extracts. For live cells and spheroplasts, the viscosity was measured at both room temperature (23°C) and the E. coli growth temperature (37°C), while the membrane extract liposomes were studied over a range of measurement temperatures (5–40°C). At 37°C, we recorded a membrane viscosity in live E. coli cells of 950 cP, which is considerably higher than that previously observed in other live cell membranes (e.g., eukaryotic cells, membranes of Bacillus vegetative cells). Interestingly, this indicates that E. coli cells exhibit a high degree of lipid ordering within their liquid-phase plasma membranes.
机译:粘度是细胞膜内非常重要的参数,影响小分子的扩散,因此控制细胞内反应的速率。对膜粘度的直接,定量评估引起了极大的兴趣。在这里,我们报告了在活的大肠杆菌细菌膜中使用分子转子BODIPY C10的荧光寿命成像显微镜,以直接量化粘度。使用这种方法,我们研究了由大肠杆菌膜提取物制成的活大肠杆菌细胞,原生质球和脂质体中的粘度。对于活细胞和原生质球,在室温(23°C)和大肠杆菌生长温度(37°C)时均测量粘度,同时在一系列测量温度(5-40°C)下研究膜提取脂质体C)。在37°C下,我们在活的大肠杆菌细胞中记录的膜粘度为950 cP,这比以前在其他活细胞膜(例如真核细胞,芽孢杆菌营养细胞的膜)中观察到的粘度要高得多。有趣的是,这表明大肠杆菌细胞在其液相质膜中显示出高度的脂质有序性。

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