Shaib Ali H, Chouaib Abed Alrahman, Chowdhury Rajdeep, Altendorf Jonas, Mihaylov Daniel, Zhang Chi, Krah Donatus, Imani Vanessa, Spencer Russell K W, Georgiev Svilen Veselinov, Mougios Nikolaos, Monga Mehar, Reshetniak Sofiia, Mimoso Tiago, Chen Han, Fatehbasharzad Parisa, Crzan Dagmar, Saal Kim-Ann, Alawieh Mohamad Mahdi, Alawar Nadia, Eilts Janna, Kang Jinyoung, Soleimani Alireza, Müller Marcus, Pape Constantin, Alvarez Luis, Trenkwalder Claudia, Mollenhauer Brit, Outeiro Tiago F, Köster Sarah, Preobraschenski Julia, Becherer Ute, Moser Tobias, Boyden Edward S, Aricescu A Radu, Sauer Markus, Opazo Felipe, Rizzoli Silvio O
Institute for Neuro- and Sensory Physiology, University Medical Center Göttingen, Göttingen, Germany.
Department of Cellular Neurophysiology, Center for Integrative Physiology and Molecular Medicine (CIPMM), Saarland University, Homburg, Germany.
Nat Biotechnol. 2024 Oct 9. doi: 10.1038/s41587-024-02431-9.
The attainable resolution of fluorescence microscopy has reached the subnanometer range, but this technique still fails to image the morphology of single proteins or small molecular complexes. Here, we expand the specimens at least tenfold, label them with conventional fluorophores and image them with conventional light microscopes, acquiring videos in which we analyze fluorescence fluctuations. One-step nanoscale expansion (ONE) microscopy enables the visualization of the shapes of individual membrane and soluble proteins, achieving around 1-nm resolution. We show that conformational changes are readily observable, such as those undergone by the ~17-kDa protein calmodulin upon Ca binding. ONE is also applied to clinical samples, analyzing the morphology of protein aggregates in cerebrospinal fluid from persons with Parkinson disease, potentially aiding disease diagnosis. This technology bridges the gap between high-resolution structural biology techniques and light microscopy, providing new avenues for discoveries in biology and medicine.
荧光显微镜可达到的分辨率已达到亚纳米范围,但该技术仍无法对单个蛋白质或小分子复合物的形态进行成像。在此,我们将样本至少扩大十倍,用传统荧光团对其进行标记,并用传统光学显微镜对其成像,获取视频并分析其中的荧光波动。一步纳米级扩展(ONE)显微镜能够可视化单个膜蛋白和可溶性蛋白的形状,实现约1纳米的分辨率。我们表明,构象变化很容易观察到,例如约17 kDa的钙调蛋白在结合钙离子时所经历的构象变化。ONE还应用于临床样本,分析帕金森病患者脑脊液中蛋白质聚集体的形态,可能有助于疾病诊断。这项技术填补了高分辨率结构生物学技术与光学显微镜之间的差距,为生物学和医学发现提供了新途径。