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1.
EMBO J ; 28(18): 2794-802, 2009 Sep 16.
Article in English | MEDLINE | ID: mdl-19661923

ABSTRACT

Replicative DNA polymerases present an intrinsic proofreading activity during which the DNA primer chain is transferred between the polymerization and exonuclease sites of the protein. The dynamics of this primer transfer reaction during active polymerization remain poorly understood. Here we describe a single-molecule mechanical method to investigate the conformational dynamics of the intramolecular DNA primer transfer during the processive replicative activity of the Phi 29 DNA polymerase and two of its mutants. We find that mechanical tension applied to a single polymerase-DNA complex promotes the intramolecular transfer of the primer in a similar way to the incorporation of a mismatched nucleotide. The primer transfer is achieved through two novel intermediates, one a tension-sensitive and functional polymerization conformation and a second non-active state that may work as a fidelity check point for the proofreading reaction.


Subject(s)
Bacteriophages/genetics , DNA Repair , DNA Replication , DNA-Directed DNA Polymerase/metabolism , Bacteriophages/metabolism , Binding Sites , DNA/chemistry , DNA-Directed DNA Polymerase/physiology , Kinetics , Molecular Conformation , Mutation , Nucleic Acid Conformation , Optical Tweezers , Polymerase Chain Reaction , Polymers/chemistry , Protein Structure, Tertiary , Stress, Mechanical
2.
Proc Natl Acad Sci U S A ; 102(7): 2310-5, 2005 Feb 15.
Article in English | MEDLINE | ID: mdl-15701703

ABSTRACT

Stochastic effects in biomolecular systems have now been recognized as a major physiologically and evolutionarily important factor in the development and function of many living organisms. Nevertheless, they are often thought of as providing only moderate refinements to the behaviors otherwise predicted by the classical deterministic system description. In this work we show by using both analytical and numerical investigation that at least in one ubiquitous class of (bio)chemical-reaction mechanisms, enzymatic futile cycles, the external noise may induce a bistable oscillatory (dynamic switching) behavior that is both quantitatively and qualitatively different from what is predicted or possible deterministically. We further demonstrate that the noise required to produce these distinct properties can itself be caused by a set of auxiliary chemical reactions, making it feasible for biological systems of sufficient complexity to generate such behavior internally. This new stochastic dynamics then serves to confer additional functional modalities on the enzymatic futile cycle mechanism that include stochastic amplification and signaling, the characteristics of which could be controlled by both the type and parameters of the driving noise. Hence, such noise-induced phenomena may, among other roles, potentially offer a novel type of control mechanism in pathways that contain these cycles and the like units. In particular, observations of endogenous or externally driven noise-induced dynamics in regulatory networks may thus provide additional insight into their topology, structure, and kinetics.


Subject(s)
Enzymes/metabolism , Enzyme Stability , Kinetics , Models, Biological , Models, Statistical , Signal Transduction , Stochastic Processes
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