Rapid assembly of the bacteriophage T4 core replication complex on a linear primer/template construct

Proc Natl Acad Sci U S A. 1993 Nov 15;90(22):10881-5. doi: 10.1073/pnas.90.22.10881.


DNA synthesis on a primed DNA substrate by bacteriophage T4 requires the assembly of a core replication complex consisting of the T4 DNA polymerase, a single-stranded binding protein (32 protein), and the accessory proteins 44/62 and 45. In this paper, we demonstrate the successful assembly of this core complex on a short linear primer/template system at levels of accessory proteins equivalent to the concentration of primer 3' ends. The key to this assembly is the presence of streptavidin molecules bound at each end of the DNA substrate via biotin moieties incorporated into the template strand. Streptavidin serves to block the ends of the primer/template, thus preventing translocation of the accessory proteins away from the site of assembly and their subsequent dissociation from the ends of the primer/template. Complex assembly on this substrate requires ATP and the presence of both the 44/62 and 45 proteins. The time required for assembly of a full enzyme equivalent of complex in our system is approximately 2 s.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Bacterial Proteins
  • Bacteriophage T4 / growth & development*
  • Biotin
  • DNA Replication*
  • DNA-Binding Proteins / metabolism
  • DNA-Directed DNA Polymerase / metabolism
  • Macromolecular Substances
  • Streptavidin
  • Templates, Genetic
  • Viral Proteins / metabolism
  • Virus Replication*


  • Bacterial Proteins
  • DNA-Binding Proteins
  • Macromolecular Substances
  • Viral Proteins
  • gp32 protein, Enterobacteria phage T4
  • Biotin
  • Adenosine Triphosphate
  • Streptavidin
  • DNA-Directed DNA Polymerase