Co-crystal structures of the fluorogenic aptamer Beetroot show that close homology may not predict similar RNA architecture.

Publication Type:

Journal Article

Source:

Nat Commun, Volume 14, Issue 1, p.2969 (2023)

Keywords:

Dimerization, Engineering, Fluorescence, Fluorescent Dyes, Ionophores, Oligonucleotides, RNA, Vegetables, Zea mays

Abstract:

<p>Beetroot is a homodimeric in vitro selected RNA that binds and activates DFAME, a conditional fluorophore derived from GFP. It is 70% sequence-identical to the previously characterized homodimeric aptamer Corn, which binds one molecule of its cognate fluorophore DFHO at its interprotomer interface. We have now determined the Beetroot-DFAME co-crystal structure at 1.95&thinsp;Å resolution, discovering that this RNA homodimer binds two molecules of the fluorophore, at sites separated by ~30&thinsp;Å. In addition to this overall architectural difference, the local structures of the non-canonical, complex quadruplex cores of Beetroot and Corn are distinctly different, underscoring how subtle RNA sequence differences can give rise to unexpected structural divergence. Through structure-guided engineering, we generated a variant that has a 12-fold fluorescence activation selectivity switch toward DFHO. Beetroot and this variant form heterodimers and constitute the starting point for engineered tags whose through-space inter-fluorophore interaction could be used to monitor RNA dimerization.</p>

PDB: 
8EYU (Beetroot–DFAME), 8EYV (Beetroot–DFHO), 8EYW (Beetroot–ThT), and 8F0N (Beetroot A16U,U38G–DFHO)
Detector: 
EIGER2
Beamline: 
24-ID-C
24-ID-E