Melting of a DNA Helix Terminus within the Active Site of a DNA Polymerase

Remo A. Hochstrasser, Theodore E. Carver, Lawrence Sowers, David P. Millar

Research output: Contribution to journalArticle

111 Citations (Scopus)

Abstract

Accurate synthesis of DNA by polymerases is due in part to the selective removal of misincorporated nucleotides by a 3′-5′ exonuclease activity (proofreading). Proofreading by an exonuclease domain containing a single-stranded DNA binding site may involve local melting of a duplex DNA substrate. Here we use time-resolved fluorescence spectroscopy to analyze the local melting of a DNA duplex terminus induced by the Klenow fragment of DNA polymerase I. Four oligodeoxynucleotide primer/templates were prepared, each containing the fluorescent adenine analog 2-aminopurine (A*) at the primer 3′ terminus, and one of the common DNA bases opposite the A* residue. Fluorescence decays of the duplex DNAs and the single primer oligonucleotide were jointly analyzed using global analysis procedures. Four lifetime components were resolved in the duplex DNAs, representing distinct conformational states of the terminal A* residue: paired A* bases, partially stacked A* bases, and extended A* bases. The variation of the apparent fraction of paired A* bases with temperature was in accord with optical melting data, and the extent of base pairing observed in each duplex was consistent with the base-pairing preferences of A* established in other studies. These results establish that the fluorescence decay characteristics of A* can be used to examine base-pairing interactions at a DNA duplex terminus. Since the fluorescence of A* can be observed without interference from protein amino acid residues, unlike existing methods for monitoring DNA melting transitions, this method was used to examine the extent to which Klenow fragment could induce fraying at each duplex terminus. Addition of D424A mutant Klenow fragment to the primer/template DNAs decreased the fraction of paired terminal bases and increased the fraction of extended terminal bases. These results demonstrate that Klenow fragment can melt a DNA duplex terminus, resulting in a population of DNA molecules in which the primer terminus is bound in an extended single-stranded conformation. The results of this study also establish a new method for examining base-pairing interactions within DNA molecules bound to proteins.

Original languageEnglish (US)
Pages (from-to)11971-11979
Number of pages9
JournalBiochemistry
Volume33
Issue number39
DOIs
StatePublished - Oct 1 1994
Externally publishedYes

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Nucleic Acid Denaturation
DNA-Directed DNA Polymerase
DNA Polymerase I
Catalytic Domain
Melting
DNA
Base Pairing
Exonucleases
DNA Primers
Fluorescence
Freezing
2-Aminopurine
Oligodeoxyribonucleotides
Single-Stranded DNA
Fluorescence Spectrometry
Adenine
Oligonucleotides
Proteins
Nucleotides
Molecules

ASJC Scopus subject areas

  • Biochemistry

Cite this

Melting of a DNA Helix Terminus within the Active Site of a DNA Polymerase. / Hochstrasser, Remo A.; Carver, Theodore E.; Sowers, Lawrence; Millar, David P.

In: Biochemistry, Vol. 33, No. 39, 01.10.1994, p. 11971-11979.

Research output: Contribution to journalArticle

Hochstrasser, RA, Carver, TE, Sowers, L & Millar, DP 1994, 'Melting of a DNA Helix Terminus within the Active Site of a DNA Polymerase', Biochemistry, vol. 33, no. 39, pp. 11971-11979. https://doi.org/10.1021/bi00205a036
Hochstrasser, Remo A. ; Carver, Theodore E. ; Sowers, Lawrence ; Millar, David P. / Melting of a DNA Helix Terminus within the Active Site of a DNA Polymerase. In: Biochemistry. 1994 ; Vol. 33, No. 39. pp. 11971-11979.
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