A biochemical characterization of the adeno-associated virus Rep40 helicase.

Academic Article

Abstract

  • The human adeno-associated virus (AAV) has generated much enthusiasm as a transfer vector for human gene therapy. Although clinical gene therapy trials have been initiated using AAV vectors, much remains to be learned regarding the basic mechanisms of virus replication, gene expression, and virion assembly. AAV encodes four nonstructural, or replication (Rep), proteins. The Rep78 and Rep68 proteins regulate viral DNA replication, chromosomal integration, and gene expression. The Rep52 and Rep40 proteins mediate virus assembly. To better understand Rep protein function, we have expressed the Rep40 protein in Escherichia coli and purified it to near homogeneity. Like the other Rep proteins, Rep40 possesses helicase and ATPase activity. ATP is the best substrate, and Mg2+ is the most efficient divalent metal ion for helicase activity. A Lys to His mutation in the purine nucleotide-binding site results in a protein that inhibits helicase activity in a dominant negative manner. Rep40 unwinds double-stranded DNA containing a 3' single-stranded end, or blunt end, unlike the Rep68 and Rep52 enzymes, which have a strict requirement for DNA duplexes containing a 3' single-stranded end. Values for KATP in the ATPase assay are 1.1 +/- 0.2 mM and 1.2 +/- 0.2 mM in the absence and presence, respectively, of single-stranded DNA. Values for Vmax are 220 +/- 10 and 1,500 +/- 90 nmol/min/mg in the absence and presence, respectively, of single-stranded DNA. These studies provide the first enzymatic characterization of the AAV Rep40 protein and elucidate important functional differences between the AAV helicases.
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    Keywords

  • Adenosine Triphosphatases, Adenosine Triphosphate, Binding Sites, Cation Transport Proteins, DNA Helicases, DNA, Single-Stranded, DNA-Binding Proteins, Dependovirus, Dose-Response Relationship, Drug, Escherichia coli, Genes, Dominant, Histidine, Kinetics, Lysine, Magnesium, Sodium Chloride, Substrate Specificity, Temperature, Viral Proteins
  • Digital Object Identifier (doi)

    Author List

  • Collaco RF; Kalman-Maltese V; Smith AD; Dignam JD; Trempe JP
  • Start Page

  • 34011
  • End Page

  • 34017
  • Volume

  • 278
  • Issue

  • 36