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. Author manuscript; available in PMC: 2016 May 1.
Published in final edited form as: DNA Repair (Amst). 2015 Jan 31;29:16–22. doi: 10.1016/j.dnarep.2015.01.008

Fig. 5.

Fig. 5

Excision of matched and mismatched DNA by hPolε at 20 °C. A pre-incubated solution of 100 nM hPolε (●) or p261N (■) and 20 nM 5′-radiolabeled (A) D-1 or (B) M-1 DNA was rapidly mixed with Mg2+ and quenched after various times with 0.37 M EDTA. The data were fit to Eq. (3) to yield kexo. For the matched D-1 DNA (A), the measured kexo values were 0.018 ± 0.002 s−1 and 0.041 ± 0.004 s−1 for hPolε and p261N, respectively. For the mismatched M-1 DNA (B), the measured kexo values were 0.19 ± 0.03 s−1 and 1.4 ± 0.2 s−1 for hPolε and p261N, respectively.