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首页> 外文期刊>Scientific reports. >Demonstration of the Protein Involvement in Cell Electropermeabilization using Confocal Raman Microspectroscopy
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Demonstration of the Protein Involvement in Cell Electropermeabilization using Confocal Raman Microspectroscopy

机译:使用共焦拉曼微型光谱分析器的蛋白质参与细胞电晶的蛋白质

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Confocal Raman microspectroscopy was used to study the interaction between pulsed electric fields and live cells from a molecular point of view in a non-invasive and label-free manner. Raman signatures of live human adipose-derived mesenchymal stem cells exposed or not to pulsed electric fields (8 pulses, 1 000?V/cm, 100?μs, 1?Hz) were acquired at two cellular locations (nucleus and cytoplasm) and two spectral bands (600–1 800?cm?1 and 2 800–3 100?cm?1). Vibrational modes of proteins (phenylalanine and amide I) and lipids were found to be modified by the electropermeabilization process with a statistically significant difference. The relative magnitude of four phenylalanine peaks decreased in the spectra of the pulsed group. On the contrary, the relative magnitude of the amide I band at 1658?cm?1 increased by 40% when comparing pulsed and control group. No difference was found between the control and the pulsed group in the high wavenumber spectral band. Our results reveal the modification of proteins in living cells exposed to pulsed electric fields by means of confocal Raman microspectroscopy.
机译:共聚焦拉曼微穴位用于研究脉冲电场与活细胞的相互作用,以非侵入性和无标记的方式从分子的角度来看。在两个细胞位置(细胞核和细胞质)和两个细胞位置,在两个细胞位置(核和细胞质)和两个,在脉冲电场(8个脉冲,1 000℉,100μs,1℃,1℃,1μs,1℃)和两个光谱带(600-1 800?cm≤1和2 800-3 100?cm≤1)。发现蛋白质(苯丙氨酸和酰胺I)和脂质的振动模式通过具有统计学显着的差异的电晶化方法进行修饰。在脉冲组的光谱中,四个苯丙氨酸峰的相对幅度降低。相反,当比较脉冲和对照组时,酰胺I带的相对幅度在1658Ω··厘米(1658Ω·cm≤1)增加40%。在高波纹光谱带中的控制和脉冲组之间没有发现差异。我们的结果揭示了通过共聚焦拉曼微穴位接触到脉冲电场暴露于脉冲电场的活细胞中蛋白质的修饰。

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