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Rimoli, C. V.

Publications and source records attributed to Rimoli, C. V..

3 recordsLinked to original sources

Polarization MultiFocus Microscopy for volumetric super-resolution and orientation imaging of biofilaments

Accessing molecular orientation in single molecule localization microscopy (SMLM) offers valuable insights into molecular ordering and organization in biological structures. Conventional single-molecule orientation-localization microscopy (SMOLM) methods typically rely on either engineering the microscopes point-spread function (PSF) to encode the orientation information or on polarization resolved detection. While PSF engineering enables detailed orientation analysis, it often requires complex computational analysis and suffers from reduced performance in dense cellular environments due to PSF spreading and overlap. In contrast, polarization-based approaches are easier to implement and are more fit when imaging dense samples but are unable to retrieve the axial information of single molecules. To overcome this limitation, we introduce the Polarization MultiFocus Microscope (PolMFM), a novel method for simultaneously retrieving the orientation and 3D position of single molecules. PolMFM combines the orientation measurement capabilities of a 4-polarization splitting scheme with a 3-planes multifocus microscope (MFM) enabling the reconstruction of molecular 2D orientation, wobble, and axial localization in a single acquisition. Through simulations, we demonstrate that PolMFM accurately recovers both orientation and 3D position, despite PSF defocusing. Experimental validation with reference samples shows that PolMFM matches the orientation precision of 4-Polar STORM, while uniquely adding axial information. We demonstrate the power of PolMFM by resolving the orientation and 3D positions of molecules in actin filaments in fixed cells, and by revealing that chromatin in crickets undergoes major reorganization and increased ordering during spermiogenesis. These findings highlight the potential of PolMFM for high-precision, multidimensional super-resolution imaging in complex and crowded biological environments.

biophysics↗

Genetically encoded reporters of actin filament organization in living cells and tissues

The cytoskeletal protein actin is crucial for cell shape and integrity throughout eukaryotes. Actin filaments perform essential biological functions, including muscle contraction, cell division and tissue morphogenesis. These diverse activities are achieved through the ability of actin filaments to be arranged into precise architectures. Much progress has been made in defining the proteome of the actin cytoskeleton, but a detailed appreciation of the dynamic organizational state of the actin filaments themselves has been hindered by available tools. Fluorescence polarization microscopy is uniquely placed for measuring actin filament organization by exploiting the sensitivity of polarized light excitation to the orientation of fluorophores attached to actin filaments. By engineering fusions of five widely used actin localization reporters to fluorescent proteins with constrained mobility, we have succeeded in developing genetically-encoded, green- and red-fluorescent-protein-based reporters for non-invasive, quantitative measurements of actin filament organization in living cells and tissues by fluorescence polarization microscopy.

cell biology↗

4polar-STORM polarized super-resolution imaging of actin filament organization in cells

Advances in single-molecule localization microscopy are providing unprecedented insights into the nanometer-scale organization of protein assemblies in cells and thus a powerful means for interrogating biological function. However, localization imaging alone does not contain information on protein conformation and orientation, which constitute additional key signatures of protein function. Here, we present a new microscopy method which combines for the first time Stochastic Optical Reconstruction Microscopy (STORM) super-resolution imaging with single molecule orientation and wobbling measurements using a four polarization-resolved image splitting scheme. This new method, called 4polar-STORM, allows us to determine both single molecule localization and orientation in 2D and to infer their 3D orientation, and is compatible with high labelling densities and thus ideally placed for the determination of the organization of dense protein assemblies in cells. We demonstrate the potential of this new method by studying the nanometer-scale organization of dense actin filament assemblies driving cell adhesion and motility, and reveal bimodal distributions of actin filament orientations in the lamellipodium, which were previously only observed in electron microscopy studies. 4polar-STORM is fully compatible with 3D localization schemes and amenable to live-cell observations, and thus promises to provide new functional readouts by enabling nanometer-scale studies of orientational dynamics in a cellular context.

biophysics↗