Multi-photon super-linear image scanning microscopy using upconversion nanoparticles (2403.13436v1)
Abstract: Super-resolution fluorescence microscopy is of great interest in life science studies for visualizing subcellular structures at the nanometer scale. Among various kinds of super-resolution approaches, image scanning microscopy (ISM) offers a doubled resolution enhancement in a simple and straightforward manner, based on the commonly used confocal microscopes. ISM is also suitable to be integrated with multi-photon microscopy techniques, such as two-photon excitation and second-harmonic generation imaging, for deep tissue imaging, but it remains the twofold limited resolution enhancement and requires expensive femtosecond lasers. Here, we present and experimentally demonstrate the super-linear ISM (SL-ISM) to push the resolution enhancement beyond the factor of two, with a single low-power, continuous-wave, and near-infrared laser, by harnessing the emission nonlinearity within the multiphoton excitation process of lanthanide-doped upconversion nanoparticles (UCNPs). Based on a modified confocal microscope, we achieve a resolution of about 120 nm, 1/8th of the excitation wavelength. Furthermore, we demonstrate a parallel detection strategy of SL-ISM with the multifocal structured excitation pattern, to speed up the acquisition frame rate. This method suggests a new perspective for super-resolution imaging or sensing, multi-photon imaging, and deep-tissue imaging with simple, low-cost, and straightforward implementations.
- S. J. Sahl, S. W. Hell, and S. Jakobs, Fluorescence nanoscopy in cell biology, Nature Reviews Molecular Cell Biology 18, 685 (2017).
- S. W. Hell and J. Wichmann, Breaking the diffraction resolution limit by stimulated emission: stimulated-emission-depletion fluorescence microscopy, Optics Letters 19, 780 (1994).
- M. J. Rust, M. Bates, and X. Zhuang, Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (storm), Nature Methods 3, 793 (2006).
- M. G. Gustafsson, Surpassing the lateral resolution limit by a factor of two using structured illumination microscopy, Journal of Microscopy 198, 82 (2000).
- M. G. Gustafsson, Nonlinear structured-illumination microscopy: wide-field fluorescence imaging with theoretically unlimited resolution, Proceedings of the National Academy of Sciences 102, 13081 (2005).
- C. B. Müller and J. Enderlein, Image scanning microscopy, Physical Review Letters 104, 198101 (2010).
- C. J. Sheppard, S. B. Mehta, and R. Heintzmann, Superresolution by image scanning microscopy using pixel reassignment, Optics Letters 38, 2889 (2013).
- S. Wu and H.-J. Butt, Near-infrared-sensitive materials based on upconverting nanoparticles, Advanced Materials 28, 1208 (2016).
- I. Gregor and J. Enderlein, Image scanning microscopy, Current opinion in chemical biology 51, 74 (2019).
- E. N. Ward, F. H. Torkelsen, and R. Pal, Enhancing multi-spot structured illumination microscopy with fluorescence difference, Royal Society Open Science 5, 171336 (2018).