Reaching the Information Limit in Cryo- EM of Biological Macromolecules: Experimental Aspects -Robert M. Glaeser and Richard J. Hall (2011)

Slides:



Advertisements
Similar presentations
Noise in Radiographic Imaging
Advertisements

SOMO Workshop, 20th Intl AUC Conference, San Antonio, TEXAS, 25th - 30th March, 2012 Small-Angle X-ray scattering P. Vachette (IBBMC, CNRS UMR 8619 & Université.
Electron Optics Basic Introduction Bob Ashley
Yifan Cheng Department of Biochemistry and Biophysics University of California San Francisco Electron Diffraction of 2D crystals - principle and data collection.
Fire Protection Laboratory Methods Day
Groups: WA 2,4,5,7. History  The electron microscope was first invented by a team of German engineers headed by Max Knoll and physicist Ernst Ruska in.
IFFAT FATIMA UOG. ELECTRON MICROSCOPE Contents History LM Vs EM Electron microscope Principle Types of EM Application & importance.
Optical methods for semiconductor characterization Guillaume von Gastrow.
Bob Sweet Bill Furey Considerations in Collection of Anomalous Data.
Electron Microscopy Chelsea Aitken Peter Aspinall
Microscopy Boot Camp /08/25 Nikitchenko Maxim Baktash Babadi.
Optical Tweezers F scatt F grad 1. Velocity autocorrelation function from the Langevin model kinetic property property of equilibrium fluctuations For.
CHAPTER 8 (Chapter 11 in text) Characterization of Nanomaterials.
Methods: Cryo-Electron Microscopy Biochemistry 4000 Dr. Ute Kothe.
The electron microscope: the contrast transfer function (CTF) Javier Vargas Centro Nacional de Biotecnología-CSIC
Microscopes are used to increase the magnification and resolving power of the unaided eye MICROSCOPES.
Quiz 10/04/14 1. Recently, it has been possible to increase the accuracy of locating a single fluorophore (see diagram). What factors are critical to how.
Macromolecular Electron Microscopy Michael Stowell MCDB B231
Detecting Electrons: CCD vs Film Practical CryoEM Course July 26, 2005 Christopher Booth.
Protein Structure Determination Part 2 -- X-ray Crystallography.
Nano-Electronics S. Mohajerzadeh University of Tehran.
Architecture of the photosynthetic apparatus by electron microscopy Architecture of the photosynthetic apparatus by electron microscopy Egbert Boekema.
CHAPTER 3 A TOUR OF THE CELL How We Study Cells 1.Microscopes provide windows to the world of the cell 2.Cell biologists can isolate organelles to study.
CHAPTER 7 A TOUR OF THE CELL Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings Section A: How We Study Cells 1.Microscopes provide.
Microscopy. Scale Lenses and the Bending of Light light is refracted (bent) when passing from one medium to another refractive index –a measure of how.
From Exit Wave to Structure: Is the Phase Object Approximation Useless? ° University of Antwerp, Department of Physics, B-2020 Antwerp, Belgium °°NCEM,
Study of Phase-Dispersive X-Ray Imaging Tomomi Ohgaki and Ichita Endo (Hiroshima Univ.)
BROOKHAVEN SCIENCE ASSOCIATES BIW ’ 06 Lepton Beam Emittance Instrumentation Igor Pinayev National Synchrotron Light Source BNL, Upton, NY.
PHYS 430/603 material Laszlo Takacs UMBC Department of Physics
VIRUS STRUCTURE Basic rules of virus architecture, structure, and assembly are the same for all families Some structures are much more complex than others,
Advanced Biology Visualizing Cells. The Human Eye  Resolution – The minimum distance two points can be apart and still be distinguished as two separate.
Structural Study of the  12 Virus By:Elizabeth Brown.
Beam Induced Movement and DDDs Javier Vargas Centro Nacional de Biotecnología-CSIC
Chapter 4: Microscopy and Cell Structure
Molecular Cell Biology Light Microscopy in Cell Biology Cooper Modified from a 2010 lecture by Richard McIntosh, University of Colorado.
Microscopie holographique à contraste de phase quantitative dans les cellules vivantes P. Marquet 1, E. Cuche 2, J.-Y. Chatton 1, C. Depeursinge 2, P.
first compound microscope – Zacharias Jansen in 1590
SEM Scanning Electron Microscope
Chris Hall Monash Centre for Synchrotron Science Monash University, Melbourne, Australia.
1 Atomic Resolution Imaging of Carbon Nanotubes from Diffraction Intensities J.M. Zuo 1, I.A. Vartanyants 2, M. Gao 1, R. Zhang 3, L.A.Nagahara 3 1 Department.
Electron probe microanalysis Low Voltage SEM Operation Modified 9/23/10.
Solving crystals structures from HREM by crystallographic image processing Xiaodong Zou Structural Chemistry, Stockholm University.
Pattersons The “third space” of crystallography. The “phase problem”
Phase Contrast sensitive Imaging
Discussion Summary for the Challenge Wah Chiu
Chapter 1.2 Electron Microscopy.  Top photo is a light micrograph : a photograph taken with a light microscope (aka a photomicrograph)  Bottom photo.
Modulation Transfer Function (MTF)
Comparison b/w light and electron microscopes LIGHT MICROSCOPE ELECTRON MICROSCOPE Magnification can be done upto 2000 times Resolving power is less.
Scanning Transmission Electron Microscope
Brightfield Contrasting Techniques Kurt Thorn NIC.
Microscopy Group 2 Cabatit, Mendoza, Ramos, Rodriguez, Tan.
By c.Keerthana.  First described by Dutch physicist frits Zernike in  It is a type of light microscopy.  It is a contrast enhancing optical technique.
1 Opto-Acoustic Imaging 台大電機系李百祺. 2 Conventional Ultrasonic Imaging Spatial resolution is mainly determined by frequency. Fabrication of high frequency.
Light Microscope Terms and Practices.
(Chapter 7) CHEM–E5225 Electron microscopy
What is cryo EM? EM = (Transmission) Electron Microscopy
Cryo-EM Services Electron microscopy (EM) has become an extremely popular method for the ultrastructural study of macromolecules, cells and tissues. An.
Cryo-em Electron microscopy (EM) has become an extremely popular method for the ultrastructural study of macromolecules, cells and tissues. An aqueous.
Cryo-EM Services Cryo-EM Services in Creative Biostructure.
Protein Structure Determination
Hans Elmlund, Dominika Elmlund, Samy Bengio  Structure 
Volume 18, Issue 8, Pages (August 2010)
Volume 20, Issue 12, Pages (December 2012)
Single-Particle Cryo-EM at Crystallographic Resolution
Volume 18, Issue 1, Pages (January 2010)
How Cryo-EM Became so Hot
Iterative Phase Retrieval (Jianwei Miao & David Sayre)
Erika J Mancini, Felix de Haas, Stephen D Fuller  Structure 
Volume 20, Issue 11, Pages (November 2012)
Presentation transcript:

Reaching the Information Limit in Cryo- EM of Biological Macromolecules: Experimental Aspects -Robert M. Glaeser and Richard J. Hall (2011)

1. Light microscope r = 172 nm 2. Electron Microscope r =.003 nm theoretical r =.27 nm point to point in JEOL 2100 scope 3. Theoretical vs experimental limit of cryo-EM 4. Why is there a gap between them? 5. How to minimize the gap. (Mostly, ZPC) Resolving Power

How large the density difference must be for the signal to be ≥ 3σ? Density values are expressed as multiples of the density of water

Atomic resolution(3Å) information by Henderson (1995) Theoretically ideal condition : 1. Homogenous (identical) objects 2. perfect contrast transfer 2. noise free detector Specimen size to align properly : 40 kDa 1. Depends on the contrast (signal) & exposure Particle numbers for atomic res. : 12, e- exposure required for the image 2. e- exposure that damages the molecule

Atomic resolution structures for icosaheral virus Nikolaus Grigorieff and Stephen C Harrison (2011) Current Opinion in Structural Biology

Atomic resolution structures with low symmetry 1.GroEL (~840 kDa, prototypical group I chaperonin) by Ludtke et al LHe, JEOL JEM3000SFF (300kV) ~ 4 Å from 20,401 particles with D7 (x14) and C7 (x7) symmetry using EMAN 2.Mm-cpn (~960 kDa, an archaeal group II chaperonin) by Zhang et al LN2, JEOL JEM3200FSC (300kV) 4.3 Å from 29,926 with D8 (x16) symmetry using EMAN

4.0-Å resolution cryo-EM structure of the mammalian chaperonin TRiC/CCT JEM3200FSC, 300kV, 101K, 1 Mda,101,000 particles, EMAN, 2fold (4.7Å with asym) Cong et al. (2010) PNAS

In practice : 1. Specimen size : o about 800 kDa 2. Particle numbers : o millions of asymmetric units 3. Why the large gap? o Radiation sensitive object (low SNR) o Imperfect contrast transfer o Beam-induced movements o Detector o Aligning particles (reconstruction)

Object Image Model Microscopy Reconstruction Biological specimen, Heterogeneity, & Thick ice Imperfect detector, Poor CTF & Sample movement CTF-correction, Classification & Alignment

Electron exposure 1.‘‘Everything under the electron beam would burn to a cinder.’’ - Gabor (1928) 2. Radiation sensitive biological specimen limits at 2,000 e-/nm2 (20 e-/Å2) for 300 keV 3.Low SNR 4.Currently available detectors enhance noise of the low-dose images due to the imperfect detective quantum efficiency

Ideal contrast transfer

The “Object” : Biological specimen in frozen- hydrated condition 1.Weak-phase model Thin specimen with light atoms Modifies only the phase of the transmitted wave and not its intensity 2.Modest phase shift & low amplitude contrast  Low SNR 3.To enhance the contrast (signal)  Longer exposure  Averaging  Defocus  Phase Plate

Defocus (under focus) 1.Enhance the contrast 2.Poor signal transfer 1 um√3 um coherent incoherent Frank (2006)

A quarter-wave plate to apply a 90 phase shift to the scattered wave relative to the unscattered wave (Zernike, 1955) * Phase contrast is stronger at in-focus than defocus. Taylor series and assuming Φ(r) << 1, Phase shift by an object C Phase-shifted wave function 2007, Frank

Phase plate (Zernike phase contrast cryo-electron microscopy)

Chang et al. (2010) Structure : Simulated pol II images In-Focus Enhanced contrast  Higher SNR  Especially at low resolution

Simulated images of a 100 kDa enzyme embedded in vitreous ice

Epsilon15 Bacteriophage by Murata et al. (2010)

Minimizing beam-induced movement

Bacteriorhodopsin 2D crystal

Beam-induced movement : 70S ribosomes

Efforts to minimize the movement 1. Limiting the size of illuminated area. 2. Improving the electrical conductivity of the support film. 3. However, only partial reduction has been achieved.

Calculated Fourier transform of the image of a monolayer crystal of paraffin grown on a 35-nm-thick carbon film Three sets of quasi-hexagonal reflections, all at a resolution of ~0.4 nm, have essentially the full, theoretically expected amplitude THE GOAL

l Barriers for the information limit and how to reach it l 1. Imperfect DQE of the detector  Noise-free detector l Pixilated electron counter l 2. Poor CTF  Ideal phase-contrast transfer function l Charging-free quarter-wave plate l 3. Beam-induced movement  ??!! l 4. Reconstruction CTF-correction Reliable classfication (different conformational states) l Perfect alignment