cellular communication kamil růžička fgp ceitec mu genomics lectures
TRANSCRIPT
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Cellular Communication
Kamil RůžičkaFGP CEITEC MU
Genomics Lectures
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How does fluorescence work?
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How does a fluorescence microscope work?
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How does a confocal microscope work?
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Protein localizationlive imaging
Martin Chalfie
GFP discovery - Nobel Prize 2008
Roger TsienOsamu Shimomura
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GFP fusions
your genepromoterhere can be GFP
here can be GFP
terminator
your genepromoter terminator
your genepromoter terminatorhere can be GFP
N-terminal fusion
C-terminal fusion
fusion inside the coding sequence
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GFP and membrane proteins
here can be GFP
It is good to have GFP tag localized inside the cell
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Fluorescent proteins on the market
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Excitation and emission
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Multicolored fluorescent protein(neurones)
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Transport amongcompartments
Alberts et al. 2008
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Also RNA can be differentially localized
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RNA ZIP codes for localization
Mikko Frilander
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ZIP codes often motor protein bound
Mikko Frilander
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Delivering at the correct address
1. Localisation complexassembly starts already in the nucleus
2. Cytoplasmic mRNP is"matured“, nuclear export proteins removed, additional proteins attached.
3. mRNP is associatedwith motor and transport system and delivered to the destination
4. Delivered mRNP isanchored to the destination (for storage) or translated directly.
Mikko Frilander
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Localization of mRNARNA hybridization in situ
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Localization of mRNARNA hybridization in situ
• classical technique, no alternative in developmental biology
• results often clear• can be done without generating transgenic lines
• tedious• only on “dead” samples
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λN22 system
nuclear localization signal
promoter
viral RNA binding protein
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Also mRNA can be differentially localized
Ash1 mRNA localized to the tip of the daughter cell
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Also mRNA can be differentially localized
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Also mRNA can be differentially localized
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Protein localizationimmunolocalization - fluorescently
fluorescent dye attached
primary antibodies
secondary antibodies
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Protein localizationimmunolocalization - immunogold
electron microscope
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Transport amongcompartments
Alberts et al. 2008
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Protein sorting – target peptides
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Nuclear transport
nucleoporins
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Nuclear import
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Nuclear import
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Mitochondrial transport
TIM and TOM complexes decide at which side of mitochondria the protein will be transported.
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Advanced confocal techniques
• FRAP
• photoactivatable FP
• FCS
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FRAP
region of interest
Fluorescence Recovery After Photobleaching
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FRAP
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FRAP – bleaching curve
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iFRAPinverse FRAP
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iFRAP – dissociation of premRNA from specles
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FRAP - advantages
• not only proteins (also other dyes)
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• your cells are moving
• high energy needed to bleach the ROI– can damage your material– long time needed to bleach
• usually only one ROI can be observed – time consuming
FRAP – disadvantages
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FRAP derivativesFLIP
Fluorescence Loss After Photobleaching
• bleaching process is repeated during the experiment• for studying general protein turnovers in compartments• less often used
continuous bleaching here
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FRAP derivativesFLAP
Fluorescence Localization after Photobleaching
• two fluorochromes on one protein– one bleached, non bleached as control
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Intermezzo:story from a conference
even top scientists can be wrong
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Photoactivable proteins
photoactivation(UV)
non activated
activated overlay
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Photoactivable proteins
Dronpa, Kaede, Eos – probably most popular
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Photoactivable proteins
Advantages:-most elegant, most convincing
Disadvantages:-very weak signal-each material needs optimization
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Remarks
• your material is 3D
• protein de novo synthesis in some experiments (e.g. cycloheximide stops translation)
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FLIMFluorescence Life Time Imaging Microscopy
Fluorochromes•excitation spectra•emission spectra•unique lifetime
Lifetime sensitive to almost everything:•pH•ionic strength•polarity•other fluorochrome
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FLIM - applications
Protein-protein interactions(FRET-FLIM) (other lecture)
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FLIM - applications
lifetime decreased by site specific IgG injection
phosphorylation assay
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FCSFluorescence Correlation Spectroscopy
t + τ It is counted, how many times the fluorescent molecule comes through the focal plane.
autocorrelation analysisAutocorrelation analysis: the way how to discriminate the diffusions speeds of particles.
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FCS
control membrane boundGFP and RFP(crosscorrelation curve)
free GFP and RFP
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FCS
control membrane boundGFP and RFP(crosscorrelation curve)
channel crosstalk threshold
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FCS
control membrane boundGFP and RFP(crosscorrelation curve)
receptor with two labels
channel crosstalk threshold
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FCS
receptor with two labels
the crosscorelation curve is above threshold -> EGFR protein dimerizes
Liu et al., 2007