Cryo EM

Cryo-electron microscopy
Cryo-EM
Garry Taylor
www.st-andrews.ac.uk/~glt2/BL3301
Electron has a wavelength
• de Broglie relationship:
mv=h/λ or λ = h / mv
• Accelerate e- in a field of potential V, it gains energy eV which is

converted to kinetic energy:
1/2 mv2 = eV or v = ( 2eV/m)1/2
∴ λ = h / (2emV)1/2 V (kV) λ(Å)

50 0.054

100 0.037

1000 0.0087

Scanning electron
microscopy
SEM
• ~100Å beam
swept across the
surface
• ~2000Å
resolution
Transmission Electron Microscopy (TEM)
100Kev to 1 Mev electrons illuminate
whole field of view. Image is a
projection of the thin specimen.
TEM
electrons generated & focused

specimen

objective lens (forms image)

intermediate lens (switch between
imaging and diffraction modes)

projector lens (magnifies image or
diffraction pattern)

image

TEM
Interactions of electrons with matter
• 90% pass through
• Elastic scattering
– Electron interacts with Coulomb potential of
nucleus (2000 x heavier)
– Bounces off, no energy loss, same λ
• Inelastic scattering
– Electrons interact with electrons
– Energy loss, different λ, focused at different place
– Chromatic aberration
– Radiation damage - ions & reactive species
• So, use very thin specimens
Negative stain v cryo-EM
Vitrification - rapid freezing
Three main 1. Electron crystallography -

methods images and electron
diffraction patterns

of image
reconstruction
2. Single particle analysis -

identical particles viewed

in different orientations

3. Electron tomography -

multiple images of the same
specimen recorded at
different tilt angles

1. Electron crystallography –
need a regular 2D array of molecules
image enhancement by Fourier averaging
2D object with local

Typical noisy image
Electron diffraction of

3-fold symmetry
Fourier transform to
noisy image - measure

get phases
intensities of peaks

Combine 3-fold
diffraction symmetry
amplitudes average
with image image

phases

Electron crystallography
from 2D to 3D
1. Tilt sample
2. Capture image
3. Collect electron
diffraction
4. Build up 3D Fourier
space (amplitudes from
electron diffraction,
phases from Fourier
inversion of image)
5. Calculate 3D electron
density map
First success..bacteriorhodopsin
~3.5Å
resolution in
the plane,
lower
resolution
perpendicular
to the plane

Extending the method..
inducing 2D arrays
Human aquaporin
• 4Å electron diffraction
of ice-embedded 2D
crystals
• Stereo view of six

tilted transmembrane
α-helices
ATPase at 8Å resolution
Tubulin
at 3.7Å resolution
Tubulin


of image
reconstruction





2. Single particle analysis
2. Single particle
analysis
• Lower limit is 250 - 500 kDa.
• Missing cone not a problem as long as
multiple views are present
• Actually 1000s of particles
• Problem: finding relative orientation of each
particle
• First achieved with icosahedral viruses - 60 -
fold symmetry reduces number of particles
needed. 9Å resolution at best.
Hepatitis B virus
capsid
• 9Å icosahedral 3D
reconstruction from
single particles
• Model of the 149-

residue dimer that
serves as its
building block
Poliovirus and its receptor
• 21Å resolution
• virus with water soluble
ectodomain of its
receptor
• revealed binding
interactions
• allowed construction of
quasi-atomic model of
receptor, known to
consist of 3
immunoglobulin
domains
Interactions of the elongation factor with
the 70S E. coli ribosome
20Å map of ribosome (blue)

13Å map of ribosome with

and EF-G in red, from
EF-G and tRNAs

difference map

RNA polymerase
• 18Å resolution
structure of the 12-
subunit complex
Conformational changes studied by Cryo-EM
• http://people.cryst.bbk.ac.uk/~ubcg16z/
chaperone.html


of image
reconstruction





3. Electron tomography
• Multiple projections of a particle at
different angles
• Problem: electron dose
• ~1000 e nm-2 for high resolution
• ~10,000 e nm-2 for medium resolution
Cryo-ET of viruses
Herpes simplex virus

Vaccinia virus

HIV virus

100nm

2-D image reconstructed tomogram slice colored cutaway 3-D image

3D structure of eukaryotic flagella in a
quiescent state revealed by cryo-electron
tomography

Cryo EM

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Cryo-electron microscopy

• Accelerate e- in a field of potential V, it gains energy eV which is

∴ λ = h / (2emV)1/2 V (kV) λ(Å)

2. Single particle analysis -

2D object with local

• Stereo view of six

2. Single particle analysis -

• Model of the 149-

20Å map of ribosome (blue)

2. Single particle analysis -

2-D image reconstructed tomogram slice colored cutaway 3-D image

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