Search bioRxiv⌕ Search

Biology subjects

Siemons, M.

Publications and source records attributed to Siemons, M..

2 recordsLinked to original sources

3D multi-color far-red single-molecule localization microscopy with probability-based fluorophore classification

Single-Molecule Localization Microscopy remains limited in its ability for robust and simple multi-color imaging. Whereas the fluorophore Alexa647 is widely used due to its brightness and excellent blinking dynamics, other excellent blinking fluorophores, such as CF660 and CF680, spectrally overlap. Here we present Probability-based Fluorophore Classification, a method to perform multi-color SMLM with Alexa647, CF660 and CF680 that uses statistical decision theory for optimal classification. The emission is split in a short and long wavelength channel to enable classification and localization without a major loss in localization precision. Each emitter is classified using a Generalized Maximum Likelihood Ratio Test using the photon statistics of both channels. This easy-to-adopt approach does not require nanometer channel registration, is able to classify fluorophores with tunable low false positive rates (<0.5%) and optimal true positive rates and outperforms traditional ratiometric spectral de-mixing and Salvaged Fluorescence. We demonstrate its applicability on a variety of samples and targets.

cell biology↗

High precision wavefront control in Point Spread Function engineering for single emitter localization

Point spread function (PSF) engineering is used in single emitter localization to measure the emitter position in 3D and possibly other parameters such as the emission color or dipole orientation as well. Advanced PSF models such as spline fits to experimental PSFs or the vectorial PSF model can be used in the corresponding localization algorithms in order to model the intricate spot shape and deformations correctly. The complexity of the optical architecture and fit model makes PSF engineering approaches particularly sensitive to optical aberrations. Here, we present a calibration and alignment protocol for fluorescence microscopes equipped with a spatial light modulator (SLM) with the goal of establishing a wavefront error well below the diffraction limit for optimum application of complex engineered PSFs. We achieve high-precision wavefront control, to a level below 20 m{lambda} wavefront aberration over a 30 minute time window after the calibration procedure, using a separate light path for calibrating the pixel-to-pixel variations of the SLM, and alignment of the SLM with respect to the optical axis and Fourier plane within 3 {micro}m (x/y) and 100 {micro}m (z) error. Aberrations are retrieved from a fit of the vectorial PSF model to a bead z-stack and compensated with a residual wavefront error comparable to the error of the SLM calibration step. This well-calibrated and corrected setup makes it possible to create complex 3D+{lambda} PSFs that fit very well to the vectorial PSF model. Proof-of-principle bead experiments show precisions below 10 nm in x, y, and{lambda} , and below 20 nm in z over an axial range of 1 {micro}m with 2000 signal photons and 12 background photons.

biophysics↗