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. 2011 May 27;6(5):e20359. doi: 10.1371/journal.pone.0020359

Figure 3. Inhibition of degradation of the doubly-labeled DNA/RNA hybrid in 30% (v/v) HeLa S100 cytosolic cell extract upon addition of DNA aptamers.

Figure 3

(A) Steady-state FRET assays showing attenuation of degradation by RNase H1-specific DNA aptamers VI-2 (red) and V-2 (green) at 500 nM concentration. No such attenuation is observed in the absence of inhibitor (orange) or when 500 nM of the negative control S1-DNA is included (blue). Solid black lines represent single-exponential fits to the data to extract rate constants. (B) Rate constants of DNA/RNA degradation as a function of VI-2 or V-2 aptamer concentration. Solid lines are fits with a hyperbolic binding equation, revealing the nanomolar binding constants for the DNA aptamers reported in the text.