fluorescence light microscopy for cell biology1 fluorescence light microscopy for cell biology...
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Fluorescence Light Microscopy
for Cell Biology
Structure within a cell
Locations of specific molecules within a cell
Traditional questions that light microscopy has addressed:
Recent advances now allow these
questions to be asked in live cells!
Why use light microscopy?
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Determine diffusion constants and binding affinities of
a molecule at a specific site within a cell.
Determine whether two molecules are interacting at a
specific time and place within a cell.
Non-traditional “biophysical” questions that light
microscopy can now address:
Much more information than just structure!
Why use light microscopy?
Outline of topics
Conventional fluorescence microscopy
Confocal microscopy
Deconvolution microscopy
Two-photon microscopy
Microscopes:
Imaging techniques:
3D time-lapse
FRAP
FRET
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Web sites for more
information and tutorials
http://microscopy.fsu.edu/primer/index.html
Molecular Expressions Optical Microscopy Primer
http://www.olympusmicro.com/primer/techniques/fluorescence/fluorhome.html
Olympus microscopy resource center
www.molecularprobes.com
Molecular Probes
Basic operating principles of a
light microscope
objective lens
specimenfocus
eyepiece
condenser
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Compound microscope design yields
magnification and resolution
Magnification
5x, 10x, 20x, 25x, 40x, 60x, 100x typically available
for microscope objectives
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Resolution is determined in part by
the imaging medium
n = refractive index of medium:
n=1.0 air; n=1.3 water; n=1.5 oil.
(for glass n=1.5)
The more light collected, the more complete is the
image, and so resolution improves.
AIR OIL
Resolution quantified by
numerical aperture (NA)
sinNAn
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What’s the resolution limit
of light microscopy?
Rayleigh criterion: d = /(2)(NA)s N nn
d/ n
d500/ .5 700. 7nmmμ]
d
Beware of empty
magnification
High NA Low NA
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Inverted Research Microscope
new
detector
old
detector
original
detector
Detector
Computer
Microscope
Microscopist
(Who needs a microscopist?)
Computer controlled
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Fluorescence Microscopy
Predominant mode of light microscopy today
Provides molecular specificity
Yields high signal to background
What is fluorescence?
Absorption of a photon with emission of
longer wavelength photon
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higher energy
(shorter wavelengths)
lower energy
(longer wavelengths)
Fluorescence is absorption of a higher energy
photon with emission of a lower energy photon
Typical spectral curves for a fluorescent
molecule used in microscopy
How do we specifically excite the molecule, and
then specifically detect its fluorescence?
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Specificity provided by filters
Filters plus a dichroic mirror
Fluorescence Microscopy
Exciter filter
Objective
SpecimenSpecimen
Dichroic mirror
Emission filter
Filters plus a dichroic mirror
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Components combined in a
small filter cube
Fluorescence Inverted Research Microscope
excitation
filters,
dichroic
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What can we see by
fluorescence microscopy?
Probes for specific biomolecules
Probes for genes
Probes for ions
Probes for specific biomolecules
Fluorescent antibodies (immunofluorescence)
Fluorescent biomarkers
cellular molecule
antibody or other binding molecule
conjugated fluorescent dye
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Chromosome axis with topo II Microtubules in an endothelial cell
Cell walls in plant cells Histone proteins (green), EGF receptor (red)
Examples of immunofluorescence
Examples of fluorescent biomarkers
Metaphase chromosomes
Nucleic acid (yellow)Apoptotic cell: Lectin
(green), nucleic acid (red)Actin filaments
(tubeworm)
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Fluorescent probes for cellular organelles
Endoplasmic reticulum Golgi
Mitochondria Lysosomes (red), Nucleus (blue)
Fluorescent probes for small
signaling molecules
calcium
(pollen tube)phosphatidyl inositol
(fibroblasts)
cAMP
(fibroblasts)
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Conclusion:
An assortment of fluorescent probes enables detection
of a variety of cellular structures and organelles.
A more limited assortment of fluorescent probes
permits detection of small signaling molecules that
regulate cell processes.
But cells are 3D!!!
How do we get a 3D image of a cell?
focus
Easy, change the focus.
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This is called optical
sectioning microscopy
Acquire a series of focal plane images that
span the depth of the cell or object of interest.
Example: collecting a 3D image ofa tiny fluorescent bead (~0.2 μm)
z
focal planes
+4 μm
+3 μm
+2 μm
+1 μm
+0 μm
-1 μm-2 μm
-3 μm
-4 μm
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3D image stack from the small
fluorescent bead
focal planes
(xy images)
xz section
The 3D bead image viewed
from the side
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But why didn’t we get -
?
xz section
xy sections
Because the lens does not collect all of
the light emitted by the specimen
Therefore the image formed is imperfect.
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So in 3D the image of a point
source always looks like this:
out-of-focus light
Out-of-focus light creates
blur in a 3D image
Image Formation
Selected focal plane image
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in focus 1 μm out-of-focus
Image of many real point sources
A real specimen is composed of many
more such point sources
3D microscopy methods to reduce
out-of-focus light
Confocal microscopy
Two-photon microscopy
Deconvolution microscopy
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Conventional fluorescence microscopy
excites the whole specimen and collects
emitted light from the whole specimen
excitation light
3D specimen
Confocal microscopy excites the whole
specimen but collects emitted light
primarily from the focal point
3D specimen
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A typical research confocal microscope
Confocal
Conventional
The result is an image with reduced haze,
improved contrast and better resolution
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3D images can also be generated
Dim specimens are harder to image by confocal
because the pinhole rejects a lot of light
In practice, the pinhole is often made larger to
generate “partially confocal” images
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Partially confocal images are a compromise
conventional fully confocal
(small pinhole)
partially confocal
(medium pinhole)
partially confocal
(large pinhole)
Conclusion
Confocal microscopy can generate high contrast
3D images of specimens.
It has been the predominant instrument for high
resolution light microscopy in the past 10 years.
Dimmer specimens are more challenging.
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Detector
Computer
Microscope
Microscopist
Easy, computer-controlled time-lapse imaging
Cells are not only 3D, they are also alive.
How do we image changes over time?
Shutter
But the cells need to be happy too.
Sophistication of the chamber depends on the
sensitivity of the cells and the duration of the imaging
experiment. pH and temperature are key variables.
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Sometimes the cells are very happy
(But our budget is not)
Even with perfect incubation conditions,
repeated light exposure causes problems
heating (?)
photobleaching
dimmer signal
free radicals
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Photobleaching is always a problem
1
4 5
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Bleaching rate depends on the dye
Ale
xa
Flu
or,
Cy3
Dyes have been optimized for bleaching and for the
laser lines available on typical confocal microscopes
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How are living cells labeled with dyes?
cell permeable dyes
microinjection of dyes
endogenous dyes
Cell permeant dyes
Fura2
Cleaved by non-specific esterases in the cell to
become impermeant, and locked in the cell.
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Fertilization-induced calcium wave in a starfish
oocyte. Confocal images every 5 sec
Calcium concentration can then be
measured in space and time
Microinjection
microinjection
needle
patch-clamped neural cell
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Microinjection is difficult and
time-consuming
Only a limited number of cells can
be injected per experiment (~100)
Endogenous probes are now the most
convenient and most widely used
Crystal structure of GFP – green fluorescent protein
-barrel
chromophore
27 kD
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Proteins of interest can be tagged with
GFP and observed in live cells
Gene for Your Protein GFP
Transform, transfect cells
Translocation of the GFP-tagged glucocorticoid
receptor from cytoplasm to nucleus
Surprising features often discovered by time-lapse
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Double or triple labeling of live cells is
feasible with GFP variants
A spectrum of markers: blue, cyan, green, yellow, red
Time-lapse imaging: a case study
from Molecular Biology of the Cell (1998) Bray et al.
How is chromatin packaged at the Mbp level
in the interphase nucleus?
And how does this packing change when a
region becomes activated?
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Cells contain ~200 tandemly repeated copies of
{MMTV - ras - BPV} and are stably transfected with
GFP-GR under tetracycline regulation.
Live-cell imaging done in a specially
developed cell line
The tandem array is visualized as a bright structure
above the background of GFP-GR in the nucleus
GFP-GR RNA FISH OVERLAY
These bright structures are the tandem array
because they produce the predicted transcript.
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How does this structure change over time as
transcription is induced?
Method: Time-Lapse Imaging
Problems
Very rapid bleaching
Cells become sick after only 10-20 images
Cells drift out of focus
Changes occur on slow time scale (~4 h) but need ~100 movies
Solutions
2D time lapse, 1 image every 15 min
Non-confocal images
Microscopist manually corrects focus during experiment
~5 data sets collected in parallel
Tools: Chambered cover slip, stage heater, conventional
fluorescence microscope with xy controlled stage
The microscope set up
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Results
Unfolding and refolding suggests fiber
packing at different densities
Conclusion
GFP and its variants have made it possible to
easily tag proteins with fluorescent markers, and
then observe the behavior of specific cellular
structures over time.