Whelan Donna R, Bell Toby D M
School of Chemistry, Monash University , Victoria, Australia , 3800.
ACS Chem Biol. 2015 Dec 18;10(12):2874-83. doi: 10.1021/acschembio.5b00754. Epub 2015 Oct 23.
Single molecule localization microscopy (SMLM) and synchrotron Fourier transform infrared (S-FTIR) spectroscopy are two techniques capable of elucidating unique and valuable biological detail. SMLM provides images of the structures and distributions of targeted biomolecules at spatial resolutions up to an order of magnitude better than the diffraction limit, whereas IR spectroscopy objectively measures the holistic biochemistry of an entire sample, thereby revealing any variations in overall composition. Both tools are currently applied extensively to detect cellular response to disease, chemical treatment, and environmental change. Here, these two techniques have been applied correlatively at the single cell level to probe the biochemistry of common fixation methods and have detected various fixation-induced losses of biomolecular composition and cellular ultrastructure. Furthermore, by extensive honing and optimizing of fixation protocols, many fixation artifacts previously considered pervasive and regularly identified using IR spectroscopy and fluorescence techniques have been avoided. Both paraformaldehyde and two-step glutaraldehyde fixation were identified as best preserving biochemistry for both SMLM and IR studies while other glutaraldehyde and methanol fixation protocols were demonstrated to cause significant biochemical changes and higher variability between samples. Moreover, the potential complementarity of the two techniques was strikingly demonstrated in the correlated detection of biochemical changes as well as in the detection of fixation-induced damage that was only revealed by one of the two techniques.
单分子定位显微镜(SMLM)和同步辐射傅里叶变换红外(S-FTIR)光谱是两种能够揭示独特且有价值的生物学细节的技术。SMLM能够以比衍射极限高一个数量级的空间分辨率提供靶向生物分子的结构和分布图像,而红外光谱则客观地测量整个样品的整体生物化学性质,从而揭示整体组成的任何变化。目前这两种工具都被广泛应用于检测细胞对疾病、化学处理和环境变化的反应。在此,这两种技术已在单细胞水平上进行了相关应用,以探究常见固定方法的生物化学性质,并检测到了各种固定诱导的生物分子组成和细胞超微结构的损失。此外,通过对固定方案的广泛优化,许多以前被认为普遍存在且经常使用红外光谱和荧光技术识别的固定伪像已被避免。多聚甲醛固定和两步戊二醛固定被确定为在SMLM和红外研究中对生物化学性质保存最好的方法,而其他戊二醛和甲醇固定方案则被证明会导致显著的生物化学变化以及样品之间更高的变异性。此外,这两种技术的潜在互补性在生化变化的相关检测以及仅由两种技术之一揭示的固定诱导损伤的检测中得到了显著体现。