Holman H Y, Martin M C, Blakely E A, Bjornstad K, McKinney W R
Center for Environmental Biotechnology, Lawrence Berkeley National Laboratory, One Cyclotron Road, Berkeley, California 94720, USA.
Biopolymers. 2000;57(6):329-35. doi: 10.1002/1097-0282(2000)57:6<329::AID-BIP20>3.0.CO;2-2.
Synchrotron radiation based Fourier transform IR (SR-FTIR) spectromicroscopy allows the study of individual living cells with a high signal to noise ratio. Here we report the use of the SR-FTIR technique to investigate changes in IR spectral features from individual human lung fibroblast (IMR-90) cells in vitro at different points in their cell cycle. Clear changes are observed in the spectral regions corresponding to proteins, DNA, and RNA as a cell changes from the G(1)-phase to the S-phase and finally into mitosis. These spectral changes include markers for the changing secondary structure of proteins in the cell, as well as variations in DNA/RNA content and packing as the cell cycle progresses. We also observe spectral features that indicate that occasional cells are undergoing various steps in the process of cell death. The dying or dead cell has a shift in the protein amide I and II bands corresponding to changing protein morphologies, and a significant increase in the intensity of an ester carbonyl C===O peak at 1743 cm(-1) is observed. Biopolymers (Biospectroscopy) 57: 329-335, 2000
基于同步辐射的傅里叶变换红外(SR-FTIR)光谱显微镜技术能够以高信噪比研究单个活细胞。在此,我们报告使用SR-FTIR技术来研究体外培养的单个正常人肺成纤维细胞(IMR-90)在细胞周期不同阶段的红外光谱特征变化。当细胞从G1期进入S期并最终进入有丝分裂期时,在对应蛋白质、DNA和RNA的光谱区域观察到明显变化。这些光谱变化包括细胞内蛋白质二级结构改变的标记,以及随着细胞周期进展DNA/RNA含量和堆积情况的变化。我们还观察到光谱特征表明偶尔有细胞正在经历细胞死亡过程中的各个步骤。濒死或死亡细胞的蛋白质酰胺I和II带发生位移,对应蛋白质形态的改变,并且在1743 cm-1处观察到酯羰基C===O峰强度显著增加。《生物聚合物(生物光谱学)》57: 329 - 335,2000