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Updated: Apr 26, 2026

Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells
Published on: December 9, 2022
Enzymatic combinatorial nucleoside deletion scanning mutagenesis of functional RNA
Katarzyna Wawrzyniak-Turek1, Claudia Höbartner
1Research Group Nucleic Acid Chemistry, Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, 37077 Göttingen, Germany. claudia.hoebartner@mpibpc.mpg.de.
Abstract:
We describe a general and simple method to identify catalytically and structurally important nucleotides in functional RNAs. Our approach is based on statistical replacement of each nucleoside with a non-nucleosidic spacer (C3 linker, Δ), followed by separation of active library variants and readout of interference effects by analysis of enzymatic primer extension reactions.
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