Interaction of Fluorescence Labeled Single-Stranded DNA with

DNA-Helicase RepA: A Photon and Fluorescence Correlation Spectroscopy ... single-stranded DNA (ssDNA) with hexameric RepA DNA-helicase (hRepA) ...
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Biochemistry 2001, 40, 7211-7218

7211

Interaction of Fluorescence Labeled Single-Stranded DNA with Hexameric DNA-Helicase RepA: A Photon and Fluorescence Correlation Spectroscopy Study† Hai Xu,‡ Joachim Frank,*,§ Ulrike Trier,| Stefanie Hammer,| Werner Schro¨der,‡ Joachim Behlke,⊥ Monika Scha¨fer-Korting,| Josef F. Holzwarth,§ and Wolfram Saenger‡ Institut fu¨ r Kristallographie, Freie UniVersita¨ t Berlin, Takustrasse 6, D-14195 Berlin, Germany, Fritz-Haber-Institut der Max-Planck-Gesellschaft, Faradayweg 4-6, D-14195 Berlin, Germany, Institut fu¨ r Pharmazie II, Abteilung fu¨ r Pharmakologie und Toxikologie, Freie UniVersita¨ t Berlin, Ko¨ nigin-Luise-Strasse 2-4, D-14195 Berlin, Germany, and Max-Delbru¨ ck-Zentrum fu¨ r Molekulare Medizin, Robert-Ro¨ ssle-Strasse 10, D-13122 Berlin, Germany ReceiVed July 5, 2000; ReVised Manuscript ReceiVed April 12, 2001

ABSTRACT: Fluorescence correlation spectroscopy (FCS) was used to characterize the interaction of fluorescence labeled single-stranded DNA (ssDNA) with hexameric RepA DNA-helicase (hRepA) encoded by plasmid RSF1010. The apparent dissociation constants, Kd(app), for the equilibrium binding of 12mer, 30mer, and 45mer ssDNA 5′-labeled with BFL to hRepA dimer in the presence of 0.5 mM ATPγS at pH 5.8 and 25 °C were determined to be 0.58 ( 0.12, 0.52 ( 0.07, and 1.66 ( 0.32 µM, respectively. Binding curves are compatible with one binding site for ssDNA present on hRepA dimer, with no indication of cooperativity. At pH 7.6 in the presence of ATPγS and at pH 5.8 in the absence of ATPγS, complex formation between ssDNA and hRepA was too weak for measuring complete binding curves by FCS. Under these conditions, the dissociation constant, Kd(app), is in the range between 10 and 250 µM. The kinetics of complex formation at pH 5.8 are faster than the time resolution (approximately 10-20 s) of FCS experiments under pseudo-first-order conditions, with respect to BFL-ssDNA. Photon correlation spectroscopy (PCS) experiments yielded, within the experimental error range, the same values for the apparent hydrodynamic radii, Rh, of hRepA dimer and its complex with ssDNA as determined by FCS (Rh ) 6.6 ( 1 nm). hRepA starts to aggregate under acidic conditions (