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. 2020 Apr 30;48(10):5639–5655. doi: 10.1093/nar/gkaa284

Table 1.

The equilibrium dissociation constants (Kd) of SA1, SA2 and EWSR1 for different RNA-containing substrates measured from fluorescence anisotropy experiments

RNA containing substrates SA1 Kd [nM] (mean ± SEM) SA2 Kd [nM] (mean ± SEM) EWSR1 [nM] (mean ± SEM)
ssRNA 25 nt (R-loop oligo) 163.7 ± 37.4 251.1 ± 3.2 134.2 ± 0.04
45 nt 6.0 ± 0.6 11.4 ± 1.2
66 nt-1 3.2 ± 0.3 7.2 ± 2.5 35.1 ± 1.8
66 nt-2 3.0 ± 0.1 5.1 ± 0.6
dsRNA substrates dsRNA (66 bp) 61.5 ± 9.3 31.2 ± 1.8 34.6 ± 6.9
dsRNA + an overhang 95.8 ± 6.1 56.8 ± 0.5 44.0 ± 1.7
Substrates related to the model R-loop RNA:DNA hybrid + overhangs 25.8 ± 3.4 23.4 ± 1.3 94.7 ± 10.7
RNA:DNA hybrid (25 bp) 58.6 ±1.5 43.3 ± 5.6
RNA:DNA hybrid (45 bp) 44.0 ± 5.9 31.7 ± 1.5 27.7 ± 4.1
Model R-loop 38.4 ± 8.7 36.0 ± 4.0 28.6 ± 0.8

K d was calculated from two to three independent experiments.