Unité Imagerie et Modélisation, Institut Pasteur, 25-28 rue du Docteur Roux, Paris, France.
UMR 3691, CNRS; C3BI, USR 3756, IP CNRS, Paris, France.
Nat Commun. 2018 Jun 19;9(1):2409. doi: 10.1038/s41467-018-04709-4.
Single molecule localization microscopy can generate 3D super-resolution images without scanning by leveraging the axial variations of normal or engineered point spread functions (PSF). Successful implementation of these approaches for extended axial ranges remains, however, challenging. We present Zernike Optimized Localization Approach in 3D (ZOLA-3D), an easy-to-use computational and optical solution that achieves optimal resolution over a tunable axial range. We use ZOLA-3D to demonstrate 3D super-resolution imaging of mitochondria, nuclear pores and microtubules in entire nuclei or cells up to ~5 μm deep.
单分子定位显微镜可以通过利用正常或工程点扩散函数(PSF)的轴向变化来生成 3D 超分辨率图像,而无需扫描。然而,成功地将这些方法应用于扩展的轴向范围仍然具有挑战性。我们提出了 Zernike 优化定位方法在 3D 中的应用(ZOLA-3D),这是一种易于使用的计算和光学解决方案,可以在可调谐的轴向范围内实现最佳分辨率。我们使用 ZOLA-3D 来演示整个细胞核或细胞中 3D 超分辨率成像的线粒体、核孔和微管,深度可达~5μm。