Fast wavefront shaping for two-photon brain imaging with multipatch correction.
Baptiste BlochetWalther AkemannSylvain GiganLaurent BourdieuPublished in: Proceedings of the National Academy of Sciences of the United States of America (2023)
Nonlinear fluorescence microscopy promotes in-vivo optical imaging of cellular structure at diffraction-limited resolution deep inside scattering biological tissues. Active compensation of tissue-induced aberrations and light scattering through adaptive wavefront correction further extends the accessible depth by restoring high resolution at large depth. However, those corrections are only valid over a very limited field of view within the angular memory effect. To overcome this limitation, we introduce an acousto-optic light modulation technique for fluorescence imaging with simultaneous wavefront correction at pixel scan speed. Biaxial wavefront corrections are first learned by adaptive optimization at multiple locations in the image field. During image acquisition, the learned corrections are then switched on the fly according to the position of the excitation focus during the raster scan. The proposed microscope is applied to in vivo transcranial neuron imaging and demonstrates multi-patch correction of thinned skull-induced aberrations and scattering at 40-kHz data acquisition speed.
Keyphrases
- high resolution
- fluorescence imaging
- optical coherence tomography
- computed tomography
- high glucose
- single molecule
- diabetic rats
- mass spectrometry
- high speed
- photodynamic therapy
- gene expression
- magnetic resonance imaging
- high frequency
- resting state
- oxidative stress
- electronic health record
- tandem mass spectrometry
- magnetic resonance
- big data
- functional connectivity
- machine learning
- genome wide
- artificial intelligence
- multiple sclerosis
- dna methylation
- endothelial cells
- high throughput
- living cells
- cerebral blood flow