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Updated: Jun 24, 2026

Three-dimensional Super Resolution Microscopy of F-actin Filaments by Interferometric PhotoActivated Localization Microscopy (iPALM)
Published on: December 1, 2016
Effect of aberration on height calibration in three-dimensional localization-based microscopy and particle tracking
1Department of Physics, Lewis-Sigler Institute for Integrative Genomics, Princeton University, 150 Carl Icahn Laboratory, Princeton, New Jersey 08544, USA.
Abstract:
Many single-particle tracking and localization-based superresolution imaging techniques use the width of a single lateral fluorescence image to estimate a molecule's axial position. This determination is often done by use of a calibration data set derived from a source adhered to a glass-water interface. However, for sources deeper in solution, aberrations will change the relationship between the image width and the axial position. We analyzed the depth-varying point spread function of a high numerical aperture objective near an index of refraction mismatch at the water-glass interface using an optical trap. In addition to the well-known focal shift, spherical aberrations cause up to 30% relative systematic error in axial position estimation. This effect is nonuniform in depth, and we find that, although molecules below the focal plane are correctly localized, molecules deeper than the focal plane are found to be lower than their actual positions.

