A comprehensive analysis of alpha- and flavivirus proteins will be undertaken to obtain detailed knowledge of the structure and function of these proteins and their relationship to their virus life cycles. Viruses from both groups are significant human pathogens and several have been identified as possible biological weapons. We will employ a high-throughput approach to examine each of the viral proteins from representative members of the two virus groups. This will be accomplished using X-ray crystallography (Chen, Rossmann, Smith) to examine the atomic structure of the viral proteins or complexes of proteins. Cryo-electron microscopy (cryo-EM) will be employed to examine the structure of the individual viruses and their intermediates in assembly and entry (Baker, Rossmann). Knowledge obtained from structural studies will be applied to molecular genetic and biochemical approaches using viruses or replicons (Kuhn, Strauss). In vitro assays will be developed to examine various aspects of the replication cycle such as RNA replication, protein processing, particle assembly, and virus fusion (Baker, Chen, Kuhn, Rossmann, Smith, Strauss). The long-term goal of this proposal is to understand the life cycles of these two virus groups at the atomic level and to translate this information into novel antiviral (Chen, Kuhn, Rossmann, Smith) and vaccine (Baker, Kuhn, Rossmann, Strauss) approaches to control human infections. The proximity of the individual laboratories on the same floor of one building permits exchange of crystallographic (Chen, Rossmann, Smith) and cryo-EM (Baker, Rossmann) expertise as well as virological and molecular biological techniques (Kuhn). Collaborations on alphaviruses and flaviviruses have been ongoing between a subset of the PIs for more than a decade (Baker, Kuhn, Rossmann) and have expanded to include a newly hired faculty member (Chen) as well as a senior crystallographic investigator (Smith). Collaborations between the Strauss laboratory and the Purdue Structural Virology Group have grown in recent years and this is reflected in the conviction that the Strauss laboratory, although removed from the Purdue environment, will contribute significantly to the long-term successes of the project.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
5P01AI055672-05
Application #
7223494
Study Section
Microbiology and Infectious Diseases B Subcommittee (MID)
Program Officer
Repik, Patricia M
Project Start
2003-09-01
Project End
2009-02-28
Budget Start
2007-03-01
Budget End
2009-02-28
Support Year
5
Fiscal Year
2007
Total Cost
$3,142,721
Indirect Cost
Name
Purdue University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
072051394
City
West Lafayette
State
IN
Country
United States
Zip Code
47907
Terwilliger, Thomas C; Bunkóczi, Gábor; Hung, Li Wei et al. (2016) Can I solve my structure by SAD phasing? Planning an experiment, scaling data and evaluating the useful anomalous correlation and anomalous signal. Acta Crystallogr D Struct Biol 72:359-74
Akey, David L; Terwilliger, Thomas C; Smith, Janet L (2016) Efficient merging of data from multiple samples for determination of anomalous substructure. Acta Crystallogr D Struct Biol 72:296-302
Terwilliger, Thomas C; Bunkóczi, Gábor; Hung, Li Wei et al. (2016) Can I solve my structure by SAD phasing? Anomalous signal in SAD phasing. Acta Crystallogr D Struct Biol 72:346-58
Yan, Rui; Edwards, Thomas J; Pankratz, Logan M et al. (2015) Simultaneous determination of sample thickness, tilt, and electron mean free path using tomographic tilt images based on Beer-Lambert law. J Struct Biol 192:287-96
Yan, Rui; Edwards, Thomas J; Pankratz, Logan M et al. (2015) A fast cross-validation method for alignment of electron tomography images based on Beer-Lambert law. J Struct Biol 192:297-306
Akey, David L; Brown, W Clay; Jose, Joyce et al. (2015) Structure-guided insights on the role of NS1 in flavivirus infection. Bioessays 37:489-94
VanBlargan, Laura A; Davis, Kaitlin A; Dowd, Kimberly A et al. (2015) Context-Dependent Cleavage of the Capsid Protein by the West Nile Virus Protease Modulates the Efficiency of Virus Assembly. J Virol 89:8632-42
Akey, David L; Brown, W Clay; Dutta, Somnath et al. (2014) Flavivirus NS1 structures reveal surfaces for associations with membranes and the immune system. Science 343:881-5
Schnettler, Esther; Tykalová, Hana; Watson, Mick et al. (2014) Induction and suppression of tick cell antiviral RNAi responses by tick-borne flaviviruses. Nucleic Acids Res 42:9436-46
Akey, David L; Brown, W Clay; Konwerski, Jamie R et al. (2014) Use of massively multiple merged data for low-resolution S-SAD phasing and refinement of flavivirus NS1. Acta Crystallogr D Biol Crystallogr 70:2719-29

Showing the most recent 10 out of 52 publications