| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Biophys J, February 2001, p. 986-993, Vol. 80, No. 2

and
*Optical Sciences Center and
Departments of
Physiology and Pharmacology, University of Arizona, Tucson, Arizona
85724 USA
The computed tomography imaging spectrometer (CTIS) is a
non-scanning instrument capable of simultaneously acquiring full spectral information (450-750 nm) from every position element within
its field of view (75 µm × 75 µm). The current spatial and
spectral sampling intervals of the spectrometer are 1.0 µm and 10 nm,
respectively. This level of resolution is adequate to resolve signal
responses from multiple fluorescence probes located within individual
cells or different locations within the same cell. Spectral imaging
results are presented from the CTIS combined with a commercial inverted
fluorescence microscope. Results demonstrate the capability of the CTIS
to monitor the spatiotemporal evolution of pH in rat insulinoma cells
loaded with SNARF-1. The ability to analyze full spectral information for two-dimensional (x, y) images allows precise evaluation
of heterogeneous physiological responses within cell populations. Due
to low signal levels, integration times up to 2 s were required. However, reasonable modifications to the instrument design will provide
higher system transmission efficiency with increased temporal and
spatial resolution. Specifically, a custom optical design including the
use of a larger format detector array is under development for a
second-generation system.
Biophys J, February 2001, p. 986-993, Vol. 80, No. 2
© 2001 by the Biophysical Society 0006-3495/01/02/986/08 $2.00
This article has been cited by other articles:
![]() |
G. Lei and R. C. MacDonald Lipid Bilayer Vesicle Fusion: Intermediates Captured by High-Speed Microfluorescence Spectroscopy Biophys. J., September 1, 2003; 85(3): 1585 - 1599. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |