Simultaneous orientation and 3D localization microscopy with a Vortex point spread function

Journal Article (2021)
Author(s)

C. N. Hulleman (TU Delft - ImPhys/Computational Imaging)

Rasmus Thorsen (TU Delft - ImPhys/Computational Imaging)

Eugene Kim (Max Planck Insitute of Biophysics, Frankfurt, Kavli institute of nanoscience Delft, TU Delft - BN/Cees Dekker Lab)

C. Dekker (Kavli institute of nanoscience Delft, TU Delft - BN/Cees Dekker Lab)

S. Stallinga (TU Delft - ImPhys/Imaging Physics)

B. Rieger (TU Delft - ImPhys/Computational Imaging)

Research Group
ImPhys/Computational Imaging
Copyright
© 2021 C.N. Hulleman, R.Ø. Thorsen, E. Kim, C. Dekker, S. Stallinga, B. Rieger
DOI related publication
https://doi.org/10.1038/s41467-021-26228-5
More Info
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Publication Year
2021
Language
English
Copyright
© 2021 C.N. Hulleman, R.Ø. Thorsen, E. Kim, C. Dekker, S. Stallinga, B. Rieger
Research Group
ImPhys/Computational Imaging
Issue number
1
Volume number
12
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Abstract

Estimating the orientation and 3D position of rotationally constrained emitters with localization microscopy typically requires polarization splitting or a large engineered Point Spread Function (PSF). Here we utilize a compact modified PSF for single molecule emitter imaging to estimate simultaneously the 3D position, dipole orientation, and degree of rotational constraint from a single 2D image. We use an affordable and commonly available phase plate, normally used for STED microscopy in the excitation light path, to alter the PSF in the emission light path. This resulting Vortex PSF does not require polarization splitting and has a compact PSF size, making it easy to implement and combine with localization microscopy techniques. In addition to a vectorial PSF fitting routine we calibrate for field-dependent aberrations which enables orientation and position estimation within 30% of the Cramér-Rao bound limit over a 66 μm field of view. We demonstrate this technique on reorienting single molecules adhered to the cover slip, λ-DNA with DNA intercalators using binding-activated localization microscopy, and we reveal periodicity on intertwined structures on supercoiled DNA.