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This work describes extreme light localization for intracellular molecular imaging and sensing with a high signal-to-noise ratio and precision. We explore localization techniques by which achievable resolution may be customized for subcellular dynamics of molecular complexes. We have also conducted plasmon-enhanced fluorescence correlation spectroscopy of cellular organelles with improved precision. The approach was extended to switching-based light localization to circumvent the diffraction limit and to use random disordered composite metallic islands for improved structured light microscopy. Extreme light localization also proves useful for enhancing Raman microscopy. Localization-based super-resolved Raman microscopy and techniques in combination with structured illumination will be discussed.
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