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Super-resolution structured-illumination microscopy (SIM) is a powerful technique that allows one to surpass the diffraction limit by up to a factor two. Yet, its practical use is hampered by its sensitivity to imaging conditions which makes it prone to reconstruction artefacts. In this work, we present FlexSIM, a flexible SIM reconstruction method capable to handle highly challenging data. Specifically, we demonstrate the ability of FlexSIM to deal with the distortion of patterns, the high level of noise encountered in live imaging, as well as out-of-focus fluorescence. Moreover, we show that FlexSIM achieves state-of-the-art performance over a variety of open SIM datasets., (© 2024 The Author(s). Journal of Microscopy published by John Wiley & Sons Ltd on behalf of Royal Microscopical Society.)

Single-particle cryo-electron microscopy (cryo-EM) reconstructs the three-dimensional (3D) structure of biomolecules from a large set of 2D projection images with random and unknown orientations. A crucial step in the single-particle cryo-EM pipeline is 3D refinement, which resolves a highresolution 3D structure from an initial approximate volume by refining the estimation of the orientation of each projection. In this work, we propose a new approach that refines the projection angles on the continuum. We formulate the optimization problem over the density map and the orientations jointly. The density map is updated using the efficient alternating-direction method of multipliers, while the orientations are updated through a semicoordinate- wise gradient descent for which we provide an explicit derivation of the gradient. Our method eliminates the requirement for a fine discretization of the orientation space and does away with the classical but computationally expensive templatematching step. Numerical results demonstrate the feasibility and performance of our approach compared to several baselines.

High resolution imaging of molecules at the cell-substrate interface is required for understanding key biological processes. Here we propose a complete pipeline for multi-angle total internal reflection fluorescence microscopy (MA-TIRF) going from instrument design and calibration procedures to numerical reconstruction. Our custom setup is endowed with a homogeneous field illumination and precise excitation beam angle. Given a set of MA-TIRF acquisitions, we deploy an efficient joint deconvolution/reconstruction algorithm based on a variational formulation of the inverse problem. This algorithm offers the possibility of using various regularizations and can run on graphics processing unit (GPU) for rapid reconstruction. Moreover, it can be easily used with other MA-TIRF devices and we provide it as an open-source software. This ensemble has enabled us to visualize and measure with unprecedented nanometric resolution, the depth of molecular components of the fibronectin assembly machinery at the basal surface of endothelial cells.

Taking benefit from recent advances in both phase retrieval and estimation of refractive indices from holographic measurements, we propose a unified framework to reconstruct them from intensity-only measurements. Our method relies on a generic and versatile formulation of the inverse problem and includes sparsity constraints. Its modularity enables the use of a variety of forward models, from simple linear ones to more sophisticated nonlinear ones, as well as various regularizers. We present reconstructions that deploy either the beam-propagation method or the iterative Lippmann-Schwinger model, combined with total-variation regularization. They suggest that our proposed (intensity-only) method can reach the same performance as reconstructions from holographic (complex) data. This is of particular interest from a practical point of view because it allows one to simplify the acquisition setup.

Optical diffraction tomography relies on solving an inverse scattering problem governed by the wave equation. Classical reconstruction algorithms are based on linear approximations of the forward model (Born or Rytov), which limits their applicability to thin samples with low refractive-index contrasts. More recent works have shown the benefit of adopting nonlinear models. They account for multiple scattering and reflections, improving the quality of reconstruction. To reduce the complexity and memory requirements of these methods, we derive an explicit formula for the Jacobian matrix of the nonlinear Lippmann-Schwinger model which lends itself to an efficient evaluation of the gradient of the data-fidelity term. This allows us to deploy efficient methods to solve the corresponding inverse problem subject to sparsity constraints.