Fluorescence microscopy applications often require specialized instruments that are optimized for different experimental goals. Here, we present a reconfigurable microscopy module that integrates highly inclined swept tile (HIST) illumination for high-sensitivity single-molecule imaging and line-scanning confocal microscopy for rapid and optically sectioned volumetric acquisition. The system shares major hardware components, including lasers, scanning optics, and detection hardware, while employing unique beam shaping pathways to enable rapid switching between modalities without realignment. We characterize the module performance by measuring the excitation beam profiles, the point spread functions (PSF), and the optical transfer functions (OTF) across 40x, 60x, and 100x magnifications and demonstrate imaging applications including diffraction-limited fixed and live-cell volumetric imaging, fluorescence recovery after photobleaching, and super-resolution DNA-PAINT and single particle tracking (SPT). We also demonstrate the capability to execute multimodal imaging workflows by performing confocal imaging for chromatin density classification correlated with SPT data of nuclear proteins with diverse functions. Together, these results demonstrate a versatile imaging platform capable of supporting complementary fluorescence imaging modalities within a single instrument.
Optical coherence tomography (OCT), well developed for retinal, intravascular, and dermatological tissue-scale imaging, affords the potential for substantially increased speed of microscopic 3D imaging as compared to confocal microscopy, whose volumetric acquisition speed is limited by the need for images at multiple c...
Two-Photon microscopy (TPM) is an intravital imaging technique with deep tissue penetration, high three-dimensional resolution and low photobleaching. However, imaging speeds have traditionally been limited because images are generated by point scanning. Recently, Spectro-Temporal Laser Imaging by Diffractive Excitatio...
C. Stock, Gregory Berg, Matthea Thielking et al.· Frontiers in Photonics· 0 citations
Image scanning microscopy (ISM) is emerging as the natural evolution of confocal laser-scanning microscopy, combining optical sectioning and a two-fold improvement in lateral resolution with high signal-to-noise ratio. Single-photon avalanche diode (SPAD) array detectors enable an effective implementation of ISM by rec...
Laurent Le, A. Zunino, E. Slenders et al.· bioRxiv· 0 citations
Two-photon microscopy (2PM) constitutes a key-enabling technology for imaging in weakly scattering specimens, delivering high-contrast signals through the quadratic dependence of fluorescence on excitation intensity. Extending 2PM to widefield or scan-less formats is attractive for rapid functional imaging. To maintain...
H. Tobón-Maya, S. Zapata-Valencia, Gladys Mínguez-Vega et al.· Journal of Physics: Photonic...· 0 citations
Multidimensional optical microscopy - extracting 3D location, orientation, and spectral information from nanoscale emitters - is key to modern nanoscience. However, this multidimensional capability requires complex instrumental setups, demanding exceptional stability and specialized expertise in optics. Here, we overco...
J. König, Christian Cierpka Institute of Micro-, Nanotechnologies et al.· 0 citations
In vivo imaging of dynamic subcellular brain structures is key to understanding several phenomena in neuroscience. However, in the fruit fly, its implementation has been hindered by a trade-off among spatial resolution, speed, photobleaching, phototoxicity, and setup complexity required to access specific target regi...
Francisco J. Tassara, M. Barella, Tomás Sebastián Fernández Troncoso et al.· ACS Photonics· 0 citations
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