Single particle analysis is an increasingly important technique for determining intermediate resolution structures of molecules and macromolecules. The overall aim of this program project is to make single particle reconstructions routine at substantially higher resolution than currently possible, and extending the resolution of certain projects to near-atomic resolution. In addition, by integrating the new package, SPARX, with x-ray crystallographic software, the process of combining x-ray and EM information will be greatly facilitated. Reconstructions at the proposed routine resolution of 8-12 Angstroms have been performed on a few particles with existing software, but only with months or years of human effort. Human time is the primary limiting factor preventing such reconstructions from becoming routine. Existing software typically requires substantial human involvement at every stage of the reconstruction. For this program project to succeed, a powerful framework for automation of the computational aspects of the project must be developed. Currently available software does not fulfill our requirements; therefore the primary focus of this project is the development of a new software system for single particle analysis that leverages existing code and our experience in software development for single particle image reconstruction and X-ray crystallography. SPARX will utilize code from EMAN, an existing single particle reconstruction suite, and other sources, and will be built around the framework provided by PHENIX, a new x-ray crystallographic software suite being developed at LBNL. This package will be fully object oriented, and fully parallelized for use on Linux clusters as well as supercomputers. It will contain a graphical user interface both for performing reconstructions, and modifying existing or designing new reconstruction algorithms.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Program Projects (P01)
Project #
5P01GM064692-02
Application #
7551163
Study Section
Special Emphasis Panel (ZRG1)
Project Start
Project End
Budget Start
2004-06-01
Budget End
2005-05-31
Support Year
2
Fiscal Year
2004
Total Cost
$179,996
Indirect Cost
Name
Lawrence Berkeley National Laboratory
Department
Type
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

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