McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA, USA.
Nat Methods. 2024 Nov;21(11):2128-2134. doi: 10.1038/s41592-024-02454-9. Epub 2024 Oct 11.
Expansion microscopy (ExM) is in increasingly widespread use throughout biology because its isotropic physical magnification enables nanoimaging on conventional microscopes. To date, ExM methods either expand specimens to a limited range (4-10× linearly) or achieve larger expansion factors through iterating the expansion process a second time (15-20× linearly). Here, we present an ExM protocol that achieves ~20× expansion (yielding <20-nm resolution on a conventional microscope) in a single expansion step, achieving the performance of iterative expansion with the simplicity of a single-shot protocol. This protocol, which we call 20ExM, supports postexpansion staining for brain tissue, which can facilitate biomolecular labeling. 20ExM may find utility in many areas of biological investigation requiring high-resolution imaging.
扩展显微镜(ExM)在生物学领域的应用越来越广泛,因为它的各向同性物理放大功能可以在传统显微镜上进行纳米成像。迄今为止,ExM 方法要么将样本扩展到有限的范围(线性约 4-10 倍),要么通过第二次迭代扩展过程来实现更大的扩展因子(线性约 15-20 倍)。在这里,我们提出了一种 ExM 方案,该方案在单次扩展步骤中实现了约 20 倍的扩展(在传统显微镜上产生<20nm 的分辨率),从而实现了迭代扩展的性能,同时具有单次拍摄方案的简单性。我们将这种方案称为 20ExM,它支持脑组织的扩展后染色,这可以方便生物分子标记。20ExM 可能在许多需要高分辨率成像的生物学研究领域有应用价值。