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Proc Natl Acad Sci U S A. 2014 Oct 21;111(42):15096-101. doi: 10.1073/pnas.1407235111. Epub 2014 Oct 6.

Single-molecule packaging initiation in real time by a viral DNA packaging machine from bacteriophage T4.

Author information

1
Department of Physics, University of Illinois at Urbana-Champaign.
2
Department of Biology, The Catholic University of America, Washington, DC 20064.
3
Department of Biology, The Catholic University of America, Washington, DC 20064 rao@cua.edu tjha@illinois.edu.
4
Department of Physics, University of Illinois at Urbana-Champaign, Howard Hughes Medical Institute, Urbana, IL 61801; and rao@cua.edu tjha@illinois.edu.

Abstract

Viral DNA packaging motors are among the most powerful molecular motors known. A variety of structural, biochemical, and single-molecule biophysical approaches have been used to understand their mechanochemistry. However, packaging initiation has been difficult to analyze because of its transient and highly dynamic nature. Here, we developed a single-molecule fluorescence assay that allowed visualization of packaging initiation and reinitiation in real time and quantification of motor assembly and initiation kinetics. We observed that a single bacteriophage T4 packaging machine can package multiple DNA molecules in bursts of activity separated by long pauses, suggesting that it switches between active and quiescent states. Multiple initiation pathways were discovered including, unexpectedly, direct DNA binding to the capsid portal followed by recruitment of motor subunits. Rapid succession of ATP hydrolysis was essential for efficient initiation. These observations have implications for the evolution of icosahedral viruses and regulation of virus assembly.

KEYWORDS:

molecular motors; single-molecule fluorescence imaging; virus packaging

PMID:
25288726
PMCID:
PMC4210281
DOI:
10.1073/pnas.1407235111
[Indexed for MEDLINE]
Free PMC Article

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