In The journal of physical chemistry. B ; h5-index 0.0
Inspired by methods that utilize chemical-mapping data to guide secondary structure prediction, we sought to develop a framework for using assigned chemical shift data to guide RNA secondary structure prediction. We first used machine learning to develop classifiers which predict the base-pairing status of individual residues in an RNA based on their assigned chemical shifts. Then, we used these base-pairing status predictions as restraints to guide RNA folding algorithms. Our results showed that we could recover the correct secondary fold of most of the 108 RNAs in our data set with remarkable accuracy. Finally, we tested whether we could use the base-pairing status predictions that we obtained from assigned chemical shift data to conditionally predict the secondary structure of RNA. To achieve this, we attempted to model two distinct conformational states of the microRNA-20b (miR-20b) and the fluoride riboswitch using assigned chemical shifts that were available for both conformational states of each of these test RNAs. For both test cases, we found that by using the base-pairing status predictions that we obtained from assigned chemical shift data as folding restraints, we could generate structures that closely resembled the known structure of the two distinct states. A command-line tool for Chemical Shifts to Base-Pairing Status (CS2BPS) predictions in RNA has been incorporated into our CS2Structure Git repository and can be accessed via: https://github.com/atfrank/CS2Structure.
Zhang Kexin, Frank Aaron Terrence