Pesce Luca, Cozzolino Marco, Lanzanò Luca, Diaspro Alberto, Bianchini Paolo
Nanoscopy and NIC Department, Istituto Italiano di Tecnologia, Genoa, Italy.
Department of Physics, University of Genoa, Genoa, Italy.
J Biophotonics. 2019 Aug;12(8):e201900018. doi: 10.1002/jbio.201900018. Epub 2019 May 28.
Expansion microscopy is a super-resolution method that allows expanding uniformly biological samples, by increasing the relative distances among fluorescent molecules labeling specific components. One of the main concerns in this approach regards the isotropic behavior at the nanoscale. The present study aims to determine the robustness of such a technique, quantifying the expansion parameters i.e. scale factor, isotropy, uniformity. Our focus is on the nuclear pore complex (NPC), as well-known nanoscale component endowed of a preserved and symmetrical structure localized on the nuclear envelope. Here, we show that Nup153 is a good reporter to quantitatively address the isotropy of the expansion process. The quantitative analysis carried out on NPCs, at different spatial scales, allows concluding that expansion microscopy can be used at the nanoscale to measure subcellular features with an accuracy from 10 to 5 nm. Therefore, it is an excellent method for structural studies of macromolecular complexes.
扩展显微镜术是一种超分辨率方法,它通过增加标记特定成分的荧光分子之间的相对距离,使生物样本均匀扩展。这种方法的一个主要关注点是纳米尺度上的各向同性行为。本研究旨在确定该技术的稳健性,量化扩展参数,即比例因子、各向同性和均匀性。我们关注的是核孔复合体(NPC),它是一种众所周知的纳米级成分,具有位于核膜上的保存完好且对称的结构。在这里,我们表明Nup153是定量解决扩展过程各向同性的良好报告分子。在不同空间尺度上对NPC进行的定量分析表明,扩展显微镜术可用于纳米尺度,以10至5纳米的精度测量亚细胞特征。因此,它是研究大分子复合体结构的一种优秀方法。