The RGD sequence in phage phi29 terminal protein is required for interaction with phi29 DNA polymerase

Virology. 1998 Aug 15;248(1):12-9. doi: 10.1006/viro.1998.9276.

Abstract

The RGD (Arg-Gly-Asp) motif functions as a recognition site for adhesive proteins responsible for a number of cell-cell interactions. Certain viruses use this sequence as a receptor-binding site by interaction with cellular integrins. To elucidate the role of the RGD sequence of the phi29 terminal protein (TP), seven modified TPs were generated by site-directed mutagenesis. Most of the TP mutants were not efficiently used as primers, leading to a reduction of the TP-dAMP complex formation in the presence of the phi29 TP-DNA template. Moreover, these mutant TPs were poorly deoxyadenylylated by phi29 DNA polymerase in the absence of template. Analysis of primer TP/DNA polymerase complex formation showed that the modified TPs were affected in the formation of the heterodimeric complex. These results indicate that the RGD sequence present in phi29 TP is primarily involved in interaction with the viral DNA polymerase.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Bacillus Phages / genetics
  • Bacillus Phages / metabolism
  • Bacillus Phages / physiology*
  • Binding Sites
  • DNA Replication*
  • DNA-Directed DNA Polymerase / metabolism*
  • Deoxyadenine Nucleotides / metabolism
  • Dimerization
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Oligopeptides*
  • Point Mutation
  • Recombinant Proteins / biosynthesis
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / metabolism
  • Templates, Genetic
  • Viral Proteins / biosynthesis
  • Viral Proteins / chemistry
  • Viral Proteins / metabolism*
  • Virus Replication

Substances

  • Deoxyadenine Nucleotides
  • Oligopeptides
  • Recombinant Proteins
  • Viral Proteins
  • terminal protein, Bacillus phage phi29
  • 2'-deoxy-5'-adenosine monophosphate
  • arginyl-glycyl-aspartic acid
  • DNA-Directed DNA Polymerase

Associated data

  • GENBANK/J02479
  • GENBANK/M11813
  • GENBANK/M22161
  • GENBANK/M33144
  • GENBANK/X96987
  • GENBANK/X99260
  • GENBANK/Y00363
  • GENBANK/Z47794