Leland Stanford Junior University

Aaron S Andalman

Samuel J Yang

Mark A Horowitz

Karl A Deisseroth

Noy Cohen

Marc Stewart Levoy

Isaac V Kauvar

William E Allen

Logan Grosenick

Michael J Broxton

Karl A Disseroth

A method for measuring the activity of one or more excitable cells, such as neurons, in a target tissue is provided. The present method may include measuring the activity of individual, selected excitable cells by projecting one or more three dimensional (3D) multi-focal laser light patterns into a target tissue containing excitable cells adapted to emit cellular electrical activity&#x2014;sensitive fluorescence, to generate a multiplexed 2D diffraction pattern of fluorescence emitted by the neurons, and resolving the multiplexed 2D diffraction pattern. Also provided herein is a system configured to perform the present method, the system including a microscope configured to project one or more 3D multi-focal laser light patterns into a target tissue using a spatial light modulator and a mirror galvanometer, and a microlens array and an image detector to record individual and multiplexed 2D diffraction patterns of light emitted from the target tissue.

Methods and devices for imaging and/or optogenetic control of light-responsive neurons

Various aspects of the present disclosure are directed toward optics and imaging. As may be implemented with one or more embodiments, an apparatus includes one or more phase masks that operate with an objective lens and a microlens array to alter a phase characteristic of light travelling in a path from a specimen, through the objective lens and microlens array and to a photosensor array. Using this approach, the specimen can be imaged with spatial resolution characteristics provided via the altered phase characteristic, which can facilitate construction of an image with enhanced resolution.

Light-field microscopy with phase masking

Growing community of inventors

San Francisco, CA, United States of America

Aaron S Andalman