Patterson George, Davidson Michael, Manley Suliana, Lippincott-Schwartz Jennifer
Biophotonics Section, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, Maryland 20892, USA.
Annu Rev Phys Chem. 2010;61:345-67. doi: 10.1146/annurev.physchem.012809.103444.
Superresolution imaging is a rapidly emerging new field of microscopy that dramatically improves the spatial resolution of light microscopy by over an order of magnitude (approximately 10-20-nm resolution), allowing biological processes to be described at the molecular scale. Here, we discuss a form of superresolution microscopy based on the controlled activation and sampling of sparse subsets of photoconvertible fluorescent molecules. In this single-molecule-based imaging approach, a wide variety of probes have proved valuable, ranging from genetically encodable photoactivatable fluorescent proteins to photoswitchable cyanine dyes. These have been used in diverse applications of superresolution imaging: from three-dimensional, multicolor molecule localization to tracking of nanometric structures and molecules in living cells. Single-molecule-based superresolution imaging thus offers exciting possibilities for obtaining molecular-scale information on biological events occurring at variable timescales.
超分辨率成像技术是显微镜学中一个迅速兴起的新领域,它能将光学显微镜的空间分辨率显著提高一个数量级以上(分辨率约为10-20纳米),从而能够在分子尺度上描述生物过程。在这里,我们讨论一种基于光转化荧光分子稀疏子集的可控激活和采样的超分辨率显微镜技术。在这种基于单分子的成像方法中,各种各样的探针已被证明具有重要价值,从可基因编码的光激活荧光蛋白到光开关花菁染料。这些探针已被用于超分辨率成像的各种应用中:从三维多色分子定位到活细胞中纳米结构和分子的追踪。因此,基于单分子的超分辨率成像为获取在不同时间尺度上发生的生物事件的分子尺度信息提供了令人兴奋的可能性。