Max Planck Institute for Biophysical Chemistry, Department of NanoBiophotonics, Am Fassberg 11, 37077 Göttingen, Germany.
Max Planck Institute for Medical Research, Department of Optical Nanoscopy, Jahnstrasse 29, 69120 Heidelberg, Germany.
Nat Rev Mol Cell Biol. 2017 Nov;18(11):685-701. doi: 10.1038/nrm.2017.71. Epub 2017 Sep 6.
Fluorescence nanoscopy uniquely combines minimally invasive optical access to the internal nanoscale structure and dynamics of cells and tissues with molecular detection specificity. While the basic physical principles of 'super-resolution' imaging were discovered in the 1990s, with initial experimental demonstrations following in 2000, the broad application of super-resolution imaging to address cell-biological questions has only more recently emerged. Nanoscopy approaches have begun to facilitate discoveries in cell biology and to add new knowledge. One current direction for method improvement is the ambition to quantitatively account for each molecule under investigation and assess true molecular colocalization patterns via multi-colour analyses. In pursuing this goal, the labelling of individual molecules to enable their visualization has emerged as a central challenge. Extending nanoscale imaging into (sliced) tissue and whole-animal contexts is a further goal. In this Review we describe the successes to date and discuss current obstacles and possibilities for further development.
荧光纳米显微镜独特地将对细胞和组织内部纳米级结构和动力学的微创光学进入与分子检测特异性相结合。虽然“超分辨率”成像的基本物理原理是在 20 世纪 90 年代发现的,并且在 2000 年之后进行了初步的实验验证,但超分辨率成像在解决细胞生物学问题方面的广泛应用直到最近才出现。纳米显微镜方法已开始促进细胞生物学的发现,并增加新知识。方法改进的一个当前方向是雄心勃勃地定量解释每个被研究的分子,并通过多色分析评估真正的分子共定位模式。在追求这一目标的过程中,对单个分子进行标记以使其可视化已成为一个核心挑战。将纳米级成像扩展到(切片)组织和整个动物的范围是另一个目标。在这篇综述中,我们描述了迄今为止的成功,并讨论了进一步发展的当前障碍和可能性。