3D single-molecule super-resolution microscopy with a tilted light sheet

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作者
Anna-Karin Gustavsson
Petar N. Petrov
Maurice Y. Lee
Yoav Shechtman
W. E. Moerner
机构
[1] Stanford University,Department of Chemistry
[2] Karolinska Institutet,Department of Biosciences and Nutrition
[3] Stanford University,Biophysics Program
[4] Technion,Biomedical Engineering Department
[5] Israel Institute of Technology,undefined
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Tilted light sheet microscopy with 3D point spread functions (TILT3D) combines a novel, tilted light sheet illumination strategy with long axial range point spread functions (PSFs) for low-background, 3D super-localization of single molecules as well as 3D super-resolution imaging in thick cells. Because the axial positions of the single emitters are encoded in the shape of each single-molecule image rather than in the position or thickness of the light sheet, the light sheet need not be extremely thin. TILT3D is built upon a standard inverted microscope and has minimal custom parts. The result is simple and flexible 3D super-resolution imaging with tens of nm localization precision throughout thick mammalian cells. We validate TILT3D for 3D super-resolution imaging in mammalian cells by imaging mitochondria and the full nuclear lamina using the double-helix PSF for single-molecule detection and the recently developed tetrapod PSFs for fiducial bead tracking and live axial drift correction.
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