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Combined Solution and Crystal Methods Reveal the Electrostatic Tethers That Provide a Flexible Platform for Replication Activities in the Bacteriophage T7 Replisome.
Foster, Brittni M; Rosenberg, Daniel; Salvo, Henry; Stephens, Kasie L; Bintz, Brittania J; Hammel, Michal; Ellenberger, Tom; Gainey, Maria D; Wallen, Jamie R.
Afiliación
  • Foster BM; Department of Chemistry & Physics , Western Carolina University , Cullowhee , North Carolina 28723 , United States.
  • Rosenberg D; Molecular Biophysics and Integrated Bioimaging , Lawrence Berkeley National Laboratory , Berkeley , California 94720 , United States.
  • Salvo H; Graduate Group in Biophysics , University of California, Berkeley , Berkeley , California 94720 , United States.
  • Stephens KL; Department of Chemistry & Physics , Western Carolina University , Cullowhee , North Carolina 28723 , United States.
  • Bintz BJ; Department of Chemistry & Physics , Western Carolina University , Cullowhee , North Carolina 28723 , United States.
  • Hammel M; Department of Chemistry & Physics , Western Carolina University , Cullowhee , North Carolina 28723 , United States.
  • Ellenberger T; Molecular Biophysics and Integrated Bioimaging , Lawrence Berkeley National Laboratory , Berkeley , California 94720 , United States.
  • Gainey MD; Department of Biochemistry and Molecular Biophysics , Washington University School of Medicine , St. Louis , Missouri 63110 , United States.
  • Wallen JR; Department of Chemistry & Physics , Western Carolina University , Cullowhee , North Carolina 28723 , United States.
Biochemistry ; 58(45): 4466-4479, 2019 11 12.
Article en En | MEDLINE | ID: mdl-31659895
Recent structural studies of the bacteriophage T7 DNA replication system have shed light on how multiple proteins assemble to copy two antiparallel DNA strands. In T7, acidic C-terminal tails of both the primase-helicase and single-stranded DNA binding protein bind to two basic patches on the DNA polymerase to aid in replisome assembly, processivity, and coordinated DNA synthesis. Although these electrostatic interactions are essential for DNA replication, the molecular details for how these tails bind the polymerase are unknown. We have determined an X-ray crystal structure of the T7 DNA polymerase bound to both a primer/template DNA and a peptide that mimics the C-terminal tail of the primase-helicase. The structure reveals that the essential C-terminal phenylalanine of the tail binds to a hydrophobic pocket that is surrounded by positive charge on the surface of the polymerase. We show that alterations of polymerase residues that engage the tail lead to defects in viral replication. In the structure, we also observe dTTP bound in the exonuclease active site and stacked against tryptophan 160. Using both primer/extension assays and high-throughput sequencing, we show how mutations in the exonuclease active site lead to defects in mismatch repair and an increase in the level of mutagenesis of the T7 genome. Finally, using small-angle X-ray scattering, we provide the first solution structures of a complex between the single-stranded DNA binding protein and the DNA polymerase and show how a single-stranded DNA binding protein dimer engages both one and two copies of DNA polymerase.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Virales / Bacteriófago T7 / ADN Polimerasa Dirigida por ADN Idioma: En Revista: Biochemistry Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Virales / Bacteriófago T7 / ADN Polimerasa Dirigida por ADN Idioma: En Revista: Biochemistry Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos