McDermott Gerry, Le Gros Mark A, Larabell Carolyn A
Department of Anatomy, University of California, San Francisco, 94158, USA.
Annu Rev Phys Chem. 2012;63:225-39. doi: 10.1146/annurev-physchem-032511-143818. Epub 2012 Jan 10.
Living cells are structured to create a range of microenvironments that support specific chemical reactions and processes. Understanding how cells function therefore requires detailed knowledge of both the subcellular architecture and the location of specific molecules within this framework. Here we review the development of two correlated cellular imaging techniques that fulfill this need. Cells are first imaged using cryogenic fluorescence microscopy to determine the location of molecules of interest that have been labeled with fluorescent tags. The same specimen is then imaged using soft X-ray tomography to generate a high-contrast, 3D reconstruction of the cells. Data from the two modalities are then combined to produce a composite, information-rich view of the cell. This correlated imaging approach can be applied across the spectrum of problems encountered in cell biology, from basic research to biotechnological and biomedical applications such as the optimization of biofuels and the development of new pharmaceuticals.
活细胞的结构能够创造一系列支持特定化学反应和过程的微环境。因此,要了解细胞如何发挥功能,就需要详细了解亚细胞结构以及特定分子在这个框架内的位置。在这里,我们回顾两种满足这一需求的相关细胞成像技术的发展情况。首先使用低温荧光显微镜对细胞进行成像,以确定已用荧光标签标记的感兴趣分子的位置。然后使用软X射线断层扫描对同一标本进行成像,以生成细胞的高对比度三维重建图像。然后将来自这两种模态的数据进行合并,以产生细胞的综合、信息丰富的视图。这种相关成像方法可应用于细胞生物学中遇到的各种问题,从基础研究到生物技术和生物医学应用,如生物燃料的优化和新药物的开发。