Unbound MEDLINE

Probing minor groove hydrogen bonding interactions between RB69 DNA polymerase and DNA.

Abstract

Minor groove hydrogen bonding (HB) interactions between DNA polymerases (pols) and N3 of purines or O2 of pyrimidines have been proposed to be essential for DNA synthesis from results obtained using various nucleoside analogues lacking the N3 or O2 contacts that interfered with primer extension. Because there has been no direct structural evidence to support this proposal, we decided to evaluate the contribution of minor groove HB interactions with family B pols. We have used RB69 DNA pol and 3-deaza-2'-deoxyadenosine (3DA), an analogue of 2-deoxyadenosine, which has the same HB pattern opposite T but with N3 replaced with a carbon atom. We then determined pre-steady-state kinetic parameters for the insertion of dAMP opposite dT using primer/templates (P/T)-containing 3DA. We also determined three structures of ternary complexes with 3DA at various positions in the duplex DNA substrate. We found that the incorporation efficiency of dAMP opposite dT decreased 10(2)-10(3)-fold even when only one minor groove HB interaction was missing. Our structures show that the HB pattern and base pair geometry of 3DA/dT is exactly the same as those of dA/dT, which makes 3DA an optimal analogue for probing minor groove HB interactions between a DNA polymerase and a nucleobase. In addition, our structures provide a rationale for the observed 10(2)-10(3)-fold decrease in the rate of nucleotide incorporation. The minor groove HB interactions between position n - 2 of the primer strand and RB69pol fix the rotomer conformations of the K706 and D621 side chains, as well as the position of metal ion A and its coordinating ligands, so that they are in the optinal orientation for DNA synthesis.

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  • Publisher Full Text
  • Authors

    Xia S, Christian TD, Wang J, Konigsberg WH

    Institution

    Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520-8114, USA.

    Source

    Biochemistry 51:21 2012 May 29 pg 4343-53

    MeSH

    Amino Acid Substitution
    Bacteriophages
    Base Sequence
    Binding Sites
    DNA
    DNA Replication
    DNA-Directed DNA Polymerase
    Hydrogen Bonding
    Kinetics
    Models, Molecular
    Mutagenesis, Site-Directed
    Nucleic Acid Conformation
    Protein Conformation
    Recombinant Proteins
    Viral Proteins

    Pub Type(s)

    Journal Article
    Research Support, N.I.H., Extramural
    Research Support, Non-U.S. Gov't

    Language

    eng

    PubMed ID

    22571765