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. 2021 Feb 4;12:793. doi: 10.1038/s41467-021-21039-0

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© The Author(s) 2021

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 4 — a Regions identified as either being bound (green) or destabilized (red) by Zα (referring to Fig. 3) are overlayed onto the predicted base-pair free energy (RNAeval⁴⁶). b Imino peak height for proton signals in AluSx1Jo, H66* (extended duplex), h43, and H25 RNAs which are destabilized due to Zα-binding are shown versus Zα concentration. c The inverse of the Zα concentration at which 90% of the imino signals disappear into the noise is shown. Peak heights in b are from 1D NMR titrations (one measurement for each RNA).