Mg2+-dependent folding of the Azoarcus ribozyme. (a) Native gel assay for folding. Uniformly 32P-labeled RNA was equilibrated 5 min at 50°C in 0–15 mM MgCl2 as described in Materials and Methods. Band I, folding intermediates; N, native RNA. (b) Mg2+ dependence of folding. The fraction native RNA (ƒN) was determined from native gels as above, footprinting, or the observed rate of self-splicing (Fig. 7). The data were fit to the Hill equation. ○, native gels (Cm = 0.22 ± 0.01 mM, nH = 1.9 ± 0.2); ▴, RNase T1 (Cm = 0.093 ± 0.004 mM, nH = 1.8 ± 0.2); ▵, Fe-EDTA (Cm = 1.9 ± 0.08 mM, nH = 1.9 ± 0.1); ⧫, kobs self-splicing (Cm = 2.4 ± 0.6 mM, nH = 1.5 ± 0.2).