In many viruses an empty """"""""prohead"""""""" is assembled and subsequently filled with DNA by the action of ATP dependent portal motor. DNA packaging occurs in many phages, herpesviruses, adenoviruses and poxvirues and it is therefore an important target for anti-viral drug development. In this application, we propose to use genetic, biochemical and biophysical approaches to expand and deepen our previous single-molecule studies of the packaging process by the portal motor of bacteriophage F29. This phage is an ideal system to investigate this process as a robust in-vitro packaging assay has been available. During the packaging process the DNA is compacted to near-crystalline density-overcoming energetic penalties due to electrostatics repulsion, DNA bending stiffness, and entropy. Because this motor is comprised of a pentameric ring of ASCE ATPases, its study will shed important light into the operation of other members of this family and of the larger superfamily of AAA+ ring ATPases, known to be responsible for a large number of cellular functions, from protein unfolding and degradation to chromosomal segregation in prokaryotes. We propose to characterize in great detail the various chemical and mechanical events during the operational cycle of each ATPase (i.e., ATP binding, hydrolysis, product release, translocation, etc) and to establish the precise timing or coordination among the cycles of the individual subunits in the ring. We will also establish the ability of the motor to generate torque, its magnitude and its generation mechanism relative to the production of linear force. These studies will be complemented by a characterization of the nature and strength of the contacts made between the DNA and the motor and its modulation during the various phases of the mechanochemical cycle. Finally, we will establish the participation of other non-catalytic elements of the motor such as the head-tail connector and the regulation of the motor's dynamics by the internal DNA pressure generated inside the capsid during the packaging process. To carry out these studies we will take advantage of state-of-the-art optical tweezers instrumentation in our laboratory. This instrument will make it possible for us to follow the packaging process with the unprecedented spatial resolution of 1A with a temporal resolution of 1 sec. Results of biophysical measurements will be integrated with structure determination by x-ray crystallography and cryo-electron microscopy (from established collaborations) and used to guide the development of models of this process.

Public Health Relevance

We propose to study the detailed molecular mechanisms of the packaging motor responsible for genome compaction in the bacteriophage 29 using genetic, biochemical and biophysical approaches. Specifically we will use a single molecule optical tweezers approach to characterize the coordination between the individual chemical cycles of the five subunits in this ring ATPase. We will also establish the ability of this motor to generate torques and the nature and strength of its interaction with the DNA. Finally, we wish to investigate how the increasing internal DNA pressure regulates the dynamics of the motor during packaging.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM071552-05
Application #
7786492
Study Section
Macromolecular Structure and Function C Study Section (MSFC)
Program Officer
Lewis, Catherine D
Project Start
2004-07-01
Project End
2014-02-28
Budget Start
2010-05-01
Budget End
2011-02-28
Support Year
5
Fiscal Year
2010
Total Cost
$531,285
Indirect Cost
Name
University of California Berkeley
Department
Miscellaneous
Type
Organized Research Units
DUNS #
124726725
City
Berkeley
State
CA
Country
United States
Zip Code
94704
Gabizon, Ronen; Lee, Antony; Vahedian-Movahed, Hanif et al. (2018) Pause sequences facilitate entry into long-lived paused states by reducing RNA polymerase transcription rates. Nat Commun 9:2930
Tafoya, Sara; Liu, Shixin; Castillo, Juan P et al. (2018) Molecular switch-like regulation enables global subunit coordination in a viral ring ATPase. Proc Natl Acad Sci U S A 115:7961-7966
Righini, Maurizio; Lee, Antony; CaƱari-Chumpitaz, Cristhian et al. (2018) Full molecular trajectories of RNA polymerase at single base-pair resolution. Proc Natl Acad Sci U S A 115:1286-1291
Lee, Antony; Tsekouras, Konstantinos; Calderon, Christopher et al. (2017) Unraveling the Thousand Word Picture: An Introduction to Super-Resolution Data Analysis. Chem Rev 117:7276-7330
Liu, Shixin; Tafoya, Sara; Bustamante, Carlos (2017) Deciphering the Molecular Mechanism of the Bacteriophage ?29 DNA Packaging Motor. Methods Mol Biol 1486:343-355
Rodriguez-Aliaga, Piere; Ramirez, Luis; Kim, Frank et al. (2016) Substrate-translocating loops regulate mechanochemical coupling and power production in AAA+ protease ClpXP. Nat Struct Mol Biol 23:974-981
Jardine, Paul J (2016) Packaging Models versus Modeling Packaging. Biophys J 110:287-288
Liu, Ninning; Chistol, Gheorghe; Bustamante, Carlos (2015) Two-subunit DNA escort mechanism and inactive subunit bypass in an ultra-fast ring ATPase. Elife 4:
Liu, Shixin; Chistol, Gheorghe; Bustamante, Carlos (2014) Mechanical operation and intersubunit coordination of ring-shaped molecular motors: insights from single-molecule studies. Biophys J 106:1844-58
Liu, Shixin; Chistol, Gheorghe; Hetherington, Craig L et al. (2014) A viral packaging motor varies its DNA rotation and step size to preserve subunit coordination as the capsid fills. Cell 157:702-713

Showing the most recent 10 out of 27 publications