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[Preprint]. 2024 Sep 9:2024.09.09.612093. [Version 1] doi: 10.1101/2024.09.09.612093

Figure 3. Contrast matching conditions and labeling scheme to probe individual DIS RNAs in complex.

Figure 3.

(A) Calculated scattering length densities (ρ) of protiated RNA (yellow), 2H(42%) RNA (teal), and perdeuterated RNA (pink). Contrast between the chosen labeling schemes are denoted as Δρ. The contrast match points (Δρ=0) between the RNAs and appropriate H2O:D2O buffer are denoted by vertical dotted lines. (B) Labeling schemes used in our SANS experiments. The protiated RNA is matched out in 65% D2O (left) and the 2H (42%) RNAs are matched out in 90% D2O (right).