The delta domain of the HK97 major capsid protein is essential for assembly

Virology. 2014 May:456-457:171-8. doi: 10.1016/j.virol.2014.03.022. Epub 2014 Apr 10.

Abstract

The 102 residue N-terminal extension of the HK97 major capsid protein, the delta domain, is normally present during the assembly of immature HK97 procapsids, but it is removed during maturation like well-known internal scaffolding proteins of other tailed phages and herpesviruses. The delta domain also shares other unusual properties usually found in other viral and phage scaffolding proteins, including its location on the inside of the capsid, a high predicted and measured α-helical content, and an additional prediction for the ability to form parallel coiled-coils. Viral scaffolding proteins are essential for capsid assembly and phage viability, so we tested whether the HK97 delta domain was essential for capsid assembly. We studied the effects of deleting all or parts of the delta domain on capsid assembly and on complementation of capsid-protein-defective phage, and our results demonstrate that the delta domain is required for HK97 capsid assembly.

Keywords: Bacteriophage assembly; Delta domain; Viral protease incorporation; Viral scaffolding proteins; Virus capsids.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Bacteriophages / genetics
  • Bacteriophages / physiology*
  • Capsid Proteins / genetics
  • Capsid Proteins / metabolism*
  • DNA Mutational Analysis
  • Protein Structure, Tertiary
  • Sequence Deletion
  • Virus Assembly*

Substances

  • Capsid Proteins