The central objective of the proposed research is to understand the molecular basis of protein recognition that leads to the assembly of viruses. This knowledge will help to identify steps in viral assembly mechanisms that are vulnerable to interference and control. The methodology involves use of novel static and dynamic Raman spectroscopic probes of protein structures and interactions.
The specific aims are as follows: (1) Identify protein conformations and side chains that regulate subunit assembly, disassembly, viral precursor formation and genome packaging at physiological conditions. (2) Identify molecular subgroups that can be altered along the viral assembly pathway by controlled changes in cellular and/or physiological factors, such as pH, ionic composition and temperature. (3) Determine dynamics of genome transcription and replication reactions and kinetics of hydrogen-isotope (H yields D) exchange reactions in viruses, viral precursors and their components. (4) Establish new qualitative and quantitative correlations between the data of Raman spectroscopy and the structures and interactions of proteins in viruses and related macromolecular assemblies.
These aims will be pursued using recently developed Raman and UV- resonance Raman methods, including: (a) polarized Raman microspectroscopy to determine side-chain orientations in viral assemblies, (b) time-resolved Raman spectroscopy to identify specific steps in viral assembly pathways, and (c) UV-resonance Raman spectroscopy for novel structural investigations of viruses and their components. Targeted for study are key virions for which complementary genetic, biochemical and structural information is available or obtainable. These include isometric viruses (HIV-l, phi6, P22, PRD1, HK97) and filamentous viruses (Ff, Pf1, Pf3, Xf, H75). The biological significance of this research program derives from the need for fundamental information about viral assembly mechanisms. Because the knowledge gained will be applicable to viruses that infect higher organisms, including humans, this research has long-term health- related benefits.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM050776-27
Application #
6369467
Study Section
Biophysical Chemistry Study Section (BBCB)
Program Officer
Wehrle, Janna P
Project Start
1987-09-01
Project End
2005-08-31
Budget Start
2001-09-01
Budget End
2002-08-31
Support Year
27
Fiscal Year
2001
Total Cost
$310,370
Indirect Cost
Name
University of Missouri Kansas City
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
800772162
City
Kansas City
State
MO
Country
United States
Zip Code
64110
Nemecek, Daniel; Stepanek, Josef; Thomas Jr, George J (2013) Raman spectroscopy of proteins and nucleoproteins. Curr Protoc Protein Sci Chapter 17:Unit17.8
Tsuboi, Masamichi; Tsunoda, Masaru; Overman, Stacy A et al. (2010) A structural model for the single-stranded DNA genome of filamentous bacteriophage Pf1. Biochemistry 49:1737-43
Nemecek, Daniel; Overman, Stacy A; Hendrix, Roger W et al. (2009) Unfolding thermodynamics of the Delta-domain in the prohead I subunit of phage HK97: determination by factor analysis of Raman spectra. J Mol Biol 385:628-41
Tsuboi, Masamichi; Benevides, James M; Thomas Jr, George J (2009) Raman tensors and their application in structural studies of biological systems. Proc Jpn Acad Ser B Phys Biol Sci 85:83-97
Nemecek, Daniel; Lander, Gabriel C; Johnson, John E et al. (2008) Assembly architecture and DNA binding of the bacteriophage P22 terminase small subunit. J Mol Biol 383:494-501
Nemecek, Daniel; Gilcrease, Eddie B; Kang, Sebyung et al. (2007) Subunit conformations and assembly states of a DNA-translocating motor: the terminase of bacteriophage P22. J Mol Biol 374:817-36
Hammel, Michal; Nemecek, Daniel; Keightley, J Andrew et al. (2007) The Staphylococcus aureus extracellular adherence protein (Eap) adopts an elongated but structured conformation in solution. Protein Sci 16:2605-17
Sun, Ying; Overman, Stacy A; Thomas Jr, George J (2007) Impact of in vitro assembly defects on in vivo function of the phage P22 portal. Virology 365:336-45
Wang, Ying A; Yu, Xiong; Overman, Stacy et al. (2006) The structure of a filamentous bacteriophage. J Mol Biol 361:209-15
Tsuboi, Masamichi; Benevides, James M; Bondre, Priya et al. (2005) Structural details of the thermophilic filamentous bacteriophage PH75 determined by polarized Raman microspectroscopy. Biochemistry 44:4861-9

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