Title: FLUORESCENT RECOVERY AFTER
1 FLUORESCENT RECOVERY AFTER
PHOTOBLEACHING Analysis
and Applications
Zareen Butt
Department of Chemistry and Biochemistry
University of Windsor
2- OVERVIEW
- Phenomenon of Photobleaching
- Fluorescent Recovery After Photobleaching
- Measure the mobility of nuclear
- proteins, macromolecular diffusion within cell
- membranes, the cytoplasm, nucleoplasm
-
3- HOW FRAP WORKS
- Molecules covalently bound to a fluorophore
- Inhomogenous fluorescent population
- Spatial separation between fluorescent moleclues
- and photobleached molecules at time 0
4Photobleached Population
Example of photobleaching in an indian muntjac
fibroblast nucleus expressing ASF/SF2 GFP
5 DATA COLLECTION
0s
10s
20s
30s
90s
6 FLUORESCENT RECOVERY CURVE
Intensity
Intensity
Time (seconds)
7Nucleoplasmic Topoisomerase I Topoisomerase IIa ß
Chromatin associated Nucleosomal Histones
Transcription Factor Estrogen Receptor Glucocorticoid Receptor
Nuclear lamina/memebrane Emerin HA-95
List of some nuclear proteins investigated
by FRAP
8- PREFRAP ANALYSIS
- Steady-State distribution in living cells
- Artifactual Distributions
- Diffused distribution
- Formation of large spherical aggregates
- Examples of these distributions illustrated for
- histone deactylase-GFP fusion proteins
9Abnormal distribution of GFP-tagged histone
deacetylases in mouse 10t1/2 cells transfected
with HDAC4-GFP (left) and HDAC3-GFP (right).
10- DATA NORMALIZATION
- The raw data must be normalized in order to
compensate for - 1) the background signal in the image
- 2) the loss of total cellular
- fluorescence due to photobleaching
- a subregion of the cell
- 3) any loss of fluorescence that
- occurs during the course of collection
- of recovery time series
11- Diffusion coefficient (measures the rate of
- movement and represents the mean squared
- displacement of proteins over time)
- Effective diffusion coefficient (does not take
into - consideration any interaction the proteins
might - undergo in the process of diffusion)
12RECENT ENZYMATIC STUDIES USING
FRAP ANALYSIS
- gp130/Jak 1 interaction
-
- Kinetics of association and the state of
activation of - GTPases in phagosomes
- Mobility of Glucocorticoid Receptor in the
nucleus - Phospholipase C-ß2 activity and mode of
- memebrane interactions in living cells
13 FRAP analysis of gp130-YFP at the plasma
membrane
14FRAP ANALYSIS OF gp-130YFP AT THE
PLASMA MEMBRANE
- Cos-7 cells transfected with a gp130-YFP
- containing expression vector
- Region of interest with a diameter of 1.3µm is
- photobleached
- As a result of double bleaching, the mobile and
- immobile fractions remains constant
15The fraction of mobile and immobile fractions
remains constant after double bleaching
16FRAP recovery curves demonstarting that Rac
2(12V) reduces fluorescent recovery rate of
GFP-PLCß2
17 Rab-GFP FRAP.
18RECENT ENZYMATIC STUDIES USING
FRAP ANALYSIS
- gp130/Jak 1 interaction
-
- Kinetics of association and the state of
activation of - GTPases in phagosomes
- Mobility of Glucocorticoid Receptor in the
nucleus - Phospholipase C-ß2 activity and mode of
- memebrane interactions in living cells
19- CONCLUSION
- In the future, FRAP combined with useful
mathematical analysis, and use of engineered
proteins will serve as an important tool to study
the mobility of molecules in living cells
20- REFERENCES
- Carrero, G., Macdonald, D., Crawford, E., Vries
de., and Hendzel, M. (2003) Methods. 29, 14-28 - Giese, B., Au-Yeung, C., Herrmann, A.,
Diefenbach, S., Haan, C., Kuster,A., Wortmann S.,
Roderburg, C., Heinrich P., Behrmann, I., and
Muller-Newen, G. (2003) The journal of
biochemistry. 278, 39205-39213 - Illenberger, C., Walliser, C., Strobel, J.,
Gutman, O., Niv, H., Gaidzik, V., Kloog Y.,
Gierschik, P., and Henis, Y. (2003) The journal
of biochemistry. 278, 8645-8652
21- Schaaf, M., and Cidlowski, J. (2003) Molecular
and Cellular Biology. 23, 1922-1934 - Vieira, O., Bucci, C., Harrison, R., Trimble,
W., Lanzetti, L., Greunberg J., Schreiber, A.,
Stahl, P., and Grinstein, S. (2003) Molecular and
Cellular Biology. 23, 2501-2514