Our goal is to develop the software technology required to use electron microscopy to determine the atomic structures of isolated macromolecular assemblies in a routine and rapid fashion. Images of a very large number of isolated (single) macromolecular particles are needed in order to achieve the signal-to-noise ratio at high resolution that is required for this goal. A data set of approximately 100,000 asymmetric units can produce a three-dimensional reconstruction at 8-12Angstroms resolution. This resolution is sufficient to insert, and adjust if necessary, atomic-resolution models of component macromolecules, whose structure would have been determined previously by other methods (X-ray or electron crystallography, or NMR spectroscopy). Even larger data sets, consisting of at least one million asymmetric units, are needed to achieve resolutions better than 5Angstroms, and ultimately to obtain 3-D reconstructions at about 3.5Angstroms, a level of resolution which is needed for de novo determination of an atomic structure. With data sets of this size, new software tools must be created in order to complete the computational work in a rapid fashion. The steps that we have identified for work within this Program Project are: (1) Single-particle software will be optimized to run on highly parallel computers, since processing of such large data sets on a single-node workstation becomes unrealistically long. (2) Computer-assisted """"""""boxing"""""""" (identification) of single particles will be improved to such an extent that tedious, human editing of galleries of candidate particles is no longer necessary. (3) Better algorithms will be developed to estimate the alignment-parameters of single particles. In addition, the Program Project will include key elements of core research and infrastructure. Experimental images will be obtained for two macromolecular assemblies whose atomic structures are already known. These reference-data are needed for the development and validation of the new software technology that the Program will create.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Program Projects (P01)
Project #
5P01GM064692-05
Application #
7239570
Study Section
Special Emphasis Panel (ZRG1-BBCB (01))
Program Officer
Flicker, Paula F
Project Start
2003-06-01
Project End
2010-05-31
Budget Start
2007-06-01
Budget End
2010-05-31
Support Year
5
Fiscal Year
2007
Total Cost
$1,723,700
Indirect Cost
Name
Lawrence Berkeley National Laboratory
Department
Biochemistry
Type
Organized Research Units
DUNS #
078576738
City
Berkeley
State
CA
Country
United States
Zip Code
94720
Hecksel, Corey W; Darrow, Michele C; Dai, Wei et al. (2016) Quantifying Variability of Manual Annotation in Cryo-Electron Tomograms. Microsc Microanal 22:487-96
Fu, Jie; Hashem, Yaser; Wower, Jacek et al. (2011) tmRNA on its way through the ribosome: two steps of resume, and what next? RNA Biol 8:586-90
Fu, Jie; Munro, James B; Blanchard, Scott C et al. (2011) Cryoelectron microscopy structures of the ribosome complex in intermediate states during tRNA translocation. Proc Natl Acad Sci U S A 108:4817-21
Fu, Jie; Hashem, Yaser; Wower, Iwona et al. (2010) Visualizing the transfer-messenger RNA as the ribosome resumes translation. EMBO J 29:3819-25
Yang, C; Jiang, W; Chen, D-H et al. (2009) Estimating contrast transfer function and associated parameters by constrained non-linear optimization. J Microsc 233:391-403
Spahn, Christian M T; Penczek, Pawel A (2009) Exploring conformational modes of macromolecular assemblies by multiparticle cryo-EM. Curr Opin Struct Biol 19:623-31
Shatsky, Maxim; Hall, Richard J; Brenner, Steven E et al. (2009) A method for the alignment of heterogeneous macromolecules from electron microscopy. J Struct Biol 166:67-78
Serysheva, Irina I; Ludtke, Steven J; Baker, Matthew L et al. (2008) Subnanometer-resolution electron cryomicroscopy-based domain models for the cytoplasmic region of skeletal muscle RyR channel. Proc Natl Acad Sci U S A 105:9610-5
Ludtke, Steven J; Baker, Matthew L; Chen, Dong-Hua et al. (2008) De novo backbone trace of GroEL from single particle electron cryomicroscopy. Structure 16:441-8
Chen, Dong-Hua; Jakana, Joanita; Liu, Xiangan et al. (2008) Achievable resolution from images of biological specimens acquired from a 4k x 4k CCD camera in a 300-kV electron cryomicroscope. J Struct Biol 163:45-52

Showing the most recent 10 out of 22 publications