Department of Chemistry, University of Minnesota, Minneapolis, Minnesota, USA; email:
Annu Rev Anal Chem (Palo Alto Calif). 2022 Jun 13;15(1):37-55. doi: 10.1146/annurev-anchem-061020-014723. Epub 2022 Mar 22.
Biological and material samples contain nanoscale heterogeneities that are unresolvable with conventional microscopy techniques. Super-resolution fluorescence methods can break the optical diffraction limit to observe these features, but they require samples to be fluorescently labeled. Over the past decade, progress has been made toward developing super-resolution techniques that do not require the use of labels. These label-free techniques span a variety of different approaches, including structured illumination, transient absorption, infrared absorption, and coherent Raman spectroscopies. Many draw inspiration from widely successful fluorescence-based techniques such as stimulated emission depletion (STED) microscopy, photoactivated localization microscopy (PALM), and stochastic optical reconstruction microscopy (STORM). In this review, we discuss the progress made in these fields along with the current challenges and prospects in reaching resolutions comparable to those achieved with fluorescence-based methods.
生物和材料样本中包含用常规显微镜技术无法分辨的纳米级异质结构。超分辨率荧光方法可以突破光学衍射极限来观察这些特征,但它们需要对样品进行荧光标记。在过去的十年中,人们已经开发出了不需要使用标记的超分辨率技术,这些无标记技术涵盖了各种不同的方法,包括结构照明、瞬态吸收、红外吸收和相干拉曼光谱学。许多方法都受到了广泛成功的荧光技术的启发,如受激发射损耗(STED)显微镜、光激活定位显微镜(PALM)和随机光学重建显微镜(STORM)。在这篇综述中,我们讨论了这些领域的进展,以及在达到与荧光方法相当的分辨率方面所面临的挑战和前景。