Clamp subunit dissociation dictates bacteriophage T4 DNA polymerase holoenzyme disassembly

Patrice Soumillion, Daniel J. Sexton, Stephen Benkovic

Research output: Contribution to journalArticle

31 Citations (Scopus)

Abstract

Clamp proteins confer processivity to the DNA polymerase during DNA replication. These oligomeric proteins are loaded onto DNA by clamp loader protein complexes in an ATP-dependent manner. The mechanism by which the trimeric bacteriophage T4 clamp protein (the 45 protein) loads and dissociates from DNA was investigated as a function of its intersubunit protein-protein interactions. These interactions were continuously monitored using a fluorescence resonance energy transfer (FRET) based assay. A cysteine mutant of the 45 protein was constructed to facilitate site-specific incorporation of a fluorescent probe at the subunit interface. This site was chosen such that FRET was observed between the introduced fluorescent probe and a tryptophan residue located on the opposing subunit. By use of this fluorescently labeled 45 protein, it was possible to obtain an estimate of an apparent trimer dissociation constant from either a cooperative (0.08 ± 0.04 μM2 at 25 °C) or a noncooperative (0.51 μM and 0.17 μM at 25 °C) model. Upon mixing the fluorescently labeled 45 protein with a 45 protein containing 4-fluorotryptophan, a nonfluorescent tryptophan analogue, subunit exchange between the two variants of the 45 protein was observed according to a reduction in intersubunit FRET. Subunit exchange rate constants measured in the presence or absence of the clamp loader (44/62 complex), the polymerase (43 protein), and/or a primer template DNA substrate demonstrate (a) that the 45 protein is not loaded onto DNA by subunit exchange and (b) that the disassembly dissociation of a stalled holoenzyme from DNA is dictated by 45 protein subunit dissociation.

Original languageEnglish (US)
Pages (from-to)1819-1827
Number of pages9
JournalBiochemistry
Volume37
Issue number7
DOIs
StatePublished - Feb 17 1998

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Bacteriophage T4
Holoenzymes
Bacteriophages
Clamping devices
DNA-Directed DNA Polymerase
Proteins
Fluorescence Resonance Energy Transfer
DNA
Loaders
Fluorescent Dyes
Tryptophan
Ion exchange
DNA Primers
Protein Subunits
Mutant Proteins
DNA Replication
Cysteine

All Science Journal Classification (ASJC) codes

  • Biochemistry

Cite this

Soumillion, Patrice ; Sexton, Daniel J. ; Benkovic, Stephen. / Clamp subunit dissociation dictates bacteriophage T4 DNA polymerase holoenzyme disassembly. In: Biochemistry. 1998 ; Vol. 37, No. 7. pp. 1819-1827.
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Clamp subunit dissociation dictates bacteriophage T4 DNA polymerase holoenzyme disassembly. / Soumillion, Patrice; Sexton, Daniel J.; Benkovic, Stephen.

In: Biochemistry, Vol. 37, No. 7, 17.02.1998, p. 1819-1827.

Research output: Contribution to journalArticle

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