help button home button Biophys. J.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH

Biophys. J. BioFAST: First Published December 13, 2004. doi:10.1529/biophysj.104.048967
© 2004 by the Biophysical Society.


A more recent version of this article appeared on March 1, 2005.
This Article
Right arrow Full Text (Rapid PDF)
Right arrow Supplemental File
Right arrow All Versions of this Article:
biophysj.104.048967v1
88/3/2126    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
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 Koyama-Honda, I.
Right arrow Articles by Kusumi, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Koyama-Honda, I.
Right arrow Articles by Kusumi, A.

SPECTROSCOPY, IMAGING, OTHER TECHNIQUES

Fluorescence imaging for monitoring the colocalization of two single molecules in living cells

Ikuko Koyama-Honda 1, Ken Ritchie 1, Takahiro Fujiwara 1, Ryota Iino 1, Hideji Murakoshi 1, Rinshi S. Kasai 1 and Akihiro Kusumi 1*

1 Japan Science and Technology Agency

* To whom correspondence should be addressed. E-mail: akusumi{at}bio.nagoya-u.ac.jp.

Submitted on July 4, 2004
Revised on August 17, 2004
Accepted on 14 October 2004


   Abstract
The interaction, binding, and colocalization of two or more molecules in living cells are essential aspects of many biological molecular processes, and single-molecule technologies for investigating these processes in live cells, if successfully developed, would become very powerful tools. Here, we developed simultaneous, dual-color, single fluorescent molecule colocalization imaging, to quantitatively detect the colocalization of two species of individual molecules. We first established a method for spatially correcting the two full images synchronously obtained in two different colors, and then for overlaying them with an accuracy of 13 nm. By further assessing the precision of the position determination, and the signal-to-noise and signal-to-background ratios, we found that two single molecules in dual color can be colocalized to within 64-100 nm (68-90 % detectability) in the membrane of live cells for GFP and Alexa633. The detectability of true colocalization at the molecular level and the erroneous inclusion of incidental approaches of two molecules as colocalization have to be compromised at different levels in each experiment, depending on its purpose. This technique was successfully demonstrated in living cells in culture, monitoring colocalization of single molecules of E-cadherin fused with GFP diffusing in the plasma membrane with single molecules of Alexa633 conjugated to anti-E-cadherin Fab externally added to the culture medium. This work established a benchmark for monitoring the colocalization of two single molecules, which can be applied to wide ranges of studies for molecular interactions, both at the levels of single molecules and collection of molecules.

Key Words: E-cadherin, GFP, colocalization, precise image overlay, single fluorescent molecule video imaging




This article has been cited by other articles:


Home page
Biophys. JHome page
Y. M. Umemura, M. Vrljic, S. Y. Nishimura, T. K. Fujiwara, K. G. N. Suzuki, and A. Kusumi
Both MHC Class II and its GPI-Anchored Form Undergo Hop Diffusion as Observed by Single-Molecule Tracking
Biophys. J., July 1, 2008; 95(1): 435 - 450.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
S. Mao, R. K. P. Benninger, Y. Yan, C. Petchprayoon, D. Jackson, C. J. Easley, D. W. Piston, and G. Marriott
Optical Lock-In Detection of FRET Using Synthetic and Genetically Encoded Optical Switches
Biophys. J., June 1, 2008; 94(11): 4515 - 4524.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
G. I. Mashanov and J. E. Molloy
Automatic Detection of Single Fluorophores in Live Cells
Biophys. J., March 15, 2007; 92(6): 2199 - 2211.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
M. J. Saxton
A Biological Interpretation of Transient Anomalous Subdiffusion. I. Qualitative Model
Biophys. J., February 15, 2007; 92(4): 1178 - 1191.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
J. W. D. Comeau, S. Costantino, and P. W. Wiseman
A Guide to Accurate Fluorescence Microscopy Colocalization Measurements
Biophys. J., December 15, 2006; 91(12): 4611 - 4622.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Copyright © 2004 by the Biophysical Society.