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Not just a pretty picture

Not just a pretty picture. 2011. Jul. 14 Hyun wook Le e. Visualization and Representation. Which program do you want to use? At which density (contour) level are you going to present your structure? How will you show people what you see?. 105 softwares!.

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Not just a pretty picture

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  1. Not just a pretty picture 2011. Jul. 14 Hyunwook Lee

  2. Visualization and Representation • Which program do you want to use? • At which density (contour) level are you going to present your structure? • How will you show people what you see?

  3. 105 softwares! http://molvis.sdsc.edu/visres/molvisfw/titles.jsp#C

  4. Density (contour) level • Volume is very sensitive to small changes in contour level, which in turn is sensitive to scaling and CTF correction. • As a guide, workers typically need to contour at about 120% of the expected volume in order to obtain a surface that makes biological sense.

  5. EV71(+Fab) 2.0 1.0 0.5

  6. CVB3-CAR 1.0 0.5 2.0

  7. How to show them? • We should present the structure in a way which makes people can see what we see.

  8. Human Rhinovirus 14 & Fab Hansong Liu et.al (1994) JMB

  9. Different color for chemically distinct groups Rotavirus & Fab Prasad et al. 1990 Nature

  10. Cut-open views T. maritima nanocompartment http://schaechter.asmblog.org/schaechter/2011/04/beyond-the-bacterial-microcompartment.html

  11. Radially cut surface : Simian virus 40 TS Baker. 1994 PNAS

  12. Icosahedrally cut surface Infectious Bursal Disease Virus B. Bottcher et al. 1997 J of Virol

  13. Polar sections Semliki Forest Virus =  60r = 356, 296, 288, 272, 216, 196 ASD Fuller et al. 1995 Cell

  14. Radial-Depth Cueing Reovirus S.M. Spencer et al., 1997 J of Struc. Biol.

  15. Bluetongue Virus J.M.Grimes et al. 1997 Structure

  16. Reliability of Difference Imaging • Two maps must be calculated to the same resolution and scaled in such a way that the differences are minimized. • Double-check with another difference-map from independent reconstructions for same structure. • Results around symmetry axes and low radius region can mislead your interpretation.

  17. Tips : Two files in the same folder & Try to move the folder location

  18. Modeling and Comparison with X-Ray Structures Constrained fitting of an atomic model to low-resolution electron microscopic images can yield “pseudo-atomic precision” in which model atoms could, it was proposed, be placed with an accuracy of 4- to 5-fold better than the nominal experimental resolution, i.e. 4 Å detail could be interpreted from a map at 20 Å resolution. F. Fabiola et al. 2005 Structure

  19. HRV14 with Fab

  20. General outline • Absolute magnification of the reconstruction • accurate pixel size, comparison with X-ray • Matching variation in density through the reconstruction to that in the X-ray structure • Convolve x-ray structure with CTF and match resolution • If possible, mask out extra part of EM reconstruction and adjust two maps by comparing Fourier transforms of the projections of those maps • Normalize EM map for positive and same range of density values as the corresponding X-ray map • Maximum-entropy approach can be used for the treatment of CTF effects

  21. Interactive fit between the EM density and the X-ray structure • Quality of the fit : hand of the structure • Single rigid body vs multiple domains • Assessment of the quality and uniqueness of the fit • R-factor : a measure of the agreement between two maps • Refinement in reciprocal space and in real space by objective method

  22. Popular search and refinement methods • Global search for initial configuration • SITUS, COAN, and DOCKEM • Final refinement • URO, NMFF-EM, and RSRef • Methods bridging between search and refinement • EMFIT, SITUS, and CHARMM

  23. Refinement of the E. coli Ribosome in Its Initiation-like State with RSRef Real-Space Refinement Gao et al. 2003 Cell

  24. Refinement of the Myosin 10S Complex with RSRef Real-Space Refinement Liu et al. 2003 JMB

  25. Phasing of X-Ray Data with EM Data • The Phase Problem of X-ray crystallography • Classic technique to solve the Phase Problem • MIR, multiple isomorphous replacement • Useless if the crystal is not isomorphous • EM map can be used to help solve the phase problem by applying molecular replacement • Similar molecule's phases are grafted onto the intensities which are experimentally determined

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