WWW.JNEUROSCI.ORG
-
The Journal of Neuroscience
 QUICK SEARCH:   [advanced]


     
-


HOME
  |  
SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP

The Journal of Neuroscience, May 21, 2008, 28(21):5582-5593; doi:10.1523/JNEUROSCI.0055-08.2008

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental Data
Right arrow Submit an eLetter
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sjulson, L.
Right arrow Articles by Miesenböck, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sjulson, L.
Right arrow Articles by Miesenböck, G.

 Previous Article  |  Next Article 

Cellular/Molecular
Rational Optimization and Imaging In Vivo of a Genetically Encoded Optical Voltage Reporter

Lucas Sjulson1 and Gero Miesenböck1,2

1Department of Cell Biology, Yale University School of Medicine, New Haven, Connecticut 06520, and 2Department of Physiology, Anatomy, and Genetics, University of Oxford, Oxford OX1 3PT, United Kingdom

Correspondence should be addressed to Lucas Sjulson at his present address: The Rockefeller University, 1230 York Avenue, #95, New York, NY 10065. Email: lukesjulson{at}gmail.com

The hybrid voltage sensor (hVOS) combines membrane-targeted green fluorescent protein and the hydrophobic anion dipicrylamine (DPA) to provide a promising tool for optical recording of electrical activity from genetically defined populations of neurons. However, large fluorescence signals are obtained only at high DPA concentrations (>3 µM) that increase membrane capacitance to a level that suppresses neural activity. Here, we develop a quantitative model of the sensor to guide its optimization and achieved an approximate threefold increase in fractional fluorescence change at a lower DPA concentration of 2 µM. Using this optimized voltage reporter, we perform optical recordings of evoked activity in the Drosophila antennal lobe with millisecond temporal resolution but fail to detect action potentials, presumably because spike initiation and/or propagation are inhibited by the capacitive load added even at reduced DPA membrane densities. We evaluate strategies for potential further improvement of hVOS quantitatively and derive theoretical performance limits for optical voltage reporters in general.

Key words: neuroimaging; membrane potential; protein-based sensor; fluorescence; multiphoton microscopy; membrane capacitance


Received Jan. 7, 2008; revised April 10, 2008; accepted April 14, 2008.

Correspondence should be addressed to Lucas Sjulson at his present address: The Rockefeller University, 1230 York Avenue, #95, New York, NY 10065. Email: lukesjulson{at}gmail.com




This article has been cited by other articles:


Home page
ScienceHome page
G. Miesenbock
The Optogenetic Catechism
Science, October 16, 2009; 326(5951): 395 - 399.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
J. Bradley, R. Luo, T. S. Otis, and D. A. DiGregorio
Submillisecond Optical Reporting of Membrane Potential In Situ Using a Neuronal Tracer Dye
J. Neurosci., July 22, 2009; 29(29): 9197 - 9209.
[Abstract] [Full Text] [PDF]



-
-

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help

-
Copyright 2009 by Society for Neuroscience ONLINE ISSN: 1529-2401
-