Nucleic acids undergo structural
transitions to access sparsely populated and transiently lived conformational
statesor excited conformational statesthat play important
roles in diverse biological processes. Despite ever-increasing detection
of these functionally essential states, 3D structure determination
of excited states (ESs) of RNA remains elusive. This is largely due
to challenges in obtaining high-resolution structural constraints
in these ESs by conventional structural biology approaches. Here,
we present nucleic-acid-optimized chemical exchange saturation transfer
(CEST) NMR spectroscopy for measuring residual dipolar couplings (RDCs),
which provide unique long-range angular constraints in ESs of nucleic
acids. We demonstrate these approaches on a fluoride riboswitch, where
one-bond <sup>13</sup>C-<sup>1</sup>H RDCs from both base and sugar
moieties provide direct structural probes into an ES of the ligand-free
riboswitch