Simultaneous imaging of several focal planes in fluorescence microscopy for the study of cellular dynamics in 3D

Prashant Prabhat; Sripad Ram; E. Sally Ward; Raimund J. Ober

doi:10.1117/12.644343

23 February 2006 Simultaneous imaging of several focal planes in fluorescence microscopy for the study of cellular dynamics in 3D

Prashant Prabhat, Sripad Ram, E. Sally Ward, Raimund J. Ober

Author Affiliations +

Proceedings Volume 6090, Three-Dimensional and Multidimensional Microscopy: Image Acquisition and Processing XIII; 60900L (2006) https://doi.org/10.1117/12.644343
Event: SPIE BiOS, 2006, San Jose, California, United States

Abstract

Fluorescence microscopy of live cells is an important tool to investigate cellular tracking pathways. The existing microscope design is very well suited to image fast moving vesicles, tubules and organelles in one focal plane. More problematic is the imaging of cellular components that move between different focal planes. This is due to the fact that tracking of such cellular components requires that the focal plane of the microscope be changed. This has to be done with a focusing device, which is relatively slow. More importantly, only one focal plane can be imaged at a time. Therefore, while the cell is imaged at one focal plane, important events could be missed at other focal planes. To overcome these shortcomings, we present a modification of the classical microscope design with which two or more focal planes can be imaged simultaneously. In this design, the emission light collected by a single stationary objective lens is split into multiple channels. Light in each channel is focused on a CCD camera by a tube lens. By ensuring that the camera position with respect to the tube lens focal plane position is not the same in any two channels, distinct planes within the specimen can be simultaneously imaged. Here we discuss the implementation of a configuration with which four focal planes can be imaged simultaneously.

Citation Download Citation

Prashant Prabhat, Sripad Ram, E. Sally Ward, and Raimund J. Ober "Simultaneous imaging of several focal planes in fluorescence microscopy for the study of cellular dynamics in 3D", Proc. SPIE 6090, Three-Dimensional and Multidimensional Microscopy: Image Acquisition and Processing XIII, 60900L (23 February 2006); https://doi.org/10.1117/12.644343

ACCESS THE FULL ARTICLE

INSTITUTIONAL
Select your institution to access the SPIE Digital Library.

SELECT YOUR INSTITUTION

PERSONAL
Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.

PERSONAL SIGN IN

No SPIE Account? Create one

;

PURCHASE THIS CONTENT

SUBSCRIBE TO DIGITAL LIBRARY

50 downloads per 1-year subscription

Members: $195

Non-members: $335 ADD TO CART

25 downloads per 1 - year subscription

Members: $145

Non-members: $250 ADD TO CART

PURCHASE SINGLE ARTICLE