Morphogenesis of the Bacillus subtilis bacteriophage phi29 will be studied in the most efficient in vitro viral assembly system known. Protein conformational change and movement in particle assembly and DNA encapsidation will be investigated by the use of an integrated genetic, biochemical and biophysical approach. Cryo-electron microscopy and X-ray crystallography will provide a structural basis for direct measurement of the dynamic events of particle assembly. A complete model of phi morphogenesis will serve as a model for animal virus assembly and aid in the search for new antiviral therapy. Specifically, the structure of phi29 DNA packaging intermediates and intermediates in neck/tail assembly will be studied by 3D cryo-EM reconstruction; high resolution structures of the phi29 pro-head, scaffolding protein and head-tail connector will be obtained by X-ray crystallography; the phi29 pro-head will be assembled in vitro from purified proteins and chaperonins; the interaction of the phi pro-head with the super-coiled DNA-gp3-gp16 complex and the initiation and progression of packaging will be visualized by electron microscopy; the rotational motion of the head- tail connector in DNA-gp3 packaging will be measured by the use of polarized absorption relaxation after photobleaching (PARAP) and by direct visualization; and the rate of DNA-gp3 packaging in real time and the force exerted by the DNA packaging machine will be measured by the use of the laser optical trap.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
2R01DE003606-30
Application #
2852974
Study Section
Biophysical Chemistry Study Section (BBCB)
Project Start
1978-09-01
Project End
2004-03-31
Budget Start
1999-04-01
Budget End
2000-03-31
Support Year
30
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Microbiology/Immun/Virology
Type
Schools of Dentistry
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Chistol, Gheorghe; Liu, Shixin; Hetherington, Craig L et al. (2012) High degree of coordination and division of labor among subunits in a homomeric ring ATPase. Cell 151:1017-28
Grimes, Shelley; Ma, Shuhua; Gao, Jiali et al. (2011) Role of ?29 connector channel loops in late-stage DNA packaging. J Mol Biol 410:50-9
Ding, Fang; Lu, Changrui; Zhao, Wei et al. (2011) Structure and assembly of the essential RNA ring component of a viral DNA packaging motor. Proc Natl Acad Sci U S A 108:7357-62
Moffitt, Jeffrey R; Chemla, Yann R; Bustamante, Carlos (2010) Mechanistic constraints from the substrate concentration dependence of enzymatic fluctuations. Proc Natl Acad Sci U S A 107:15739-44
Aathavan, K; Politzer, Adam T; Kaplan, Ariel et al. (2009) Substrate interactions and promiscuity in a viral DNA packaging motor. Nature 461:669-73
Cohen, Daniel N; Sham, Yuk Y; Haugstad, Greg D et al. (2009) Shared catalysis in virus entry and bacterial cell wall depolymerization. J Mol Biol 387:607-18
Moffitt, Jeffrey R; Chemla, Yann R; Aathavan, K et al. (2009) Intersubunit coordination in a homomeric ring ATPase. Nature 457:446-50
Xiang, Ye; Leiman, Petr G; Li, Long et al. (2009) Crystallographic insights into the autocatalytic assembly mechanism of a bacteriophage tail spike. Mol Cell 34:375-86
Morais, Marc C; Koti, Jaya S; Bowman, Valorie D et al. (2008) Defining molecular and domain boundaries in the bacteriophage phi29 DNA packaging motor. Structure 16:1267-74
Koti, Jaya S; Morais, Marc C; Rajagopal, Raj et al. (2008) DNA packaging motor assembly intermediate of bacteriophage phi29. J Mol Biol 381:1114-32

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