
Substrate for Hairpin ribozyme cleavage studies
This 32-nucleotide RNA oligonucleotide is a synthetic substrate designed for trans-cleavage by the tobacco ringspot virus satellite RNA hairpin ribozyme. The substrate contains the conserved GUC trinucleotide cleavage motif embedded within an internal loop A context, which docks with loop B of the ribozyme to form the catalytically active loop–loop interface. Upon ribozyme recognition, cleavage occurs at the A↓GUC site, producing a 5′-hydroxyl and a 2′,3′-cyclic phosphate terminus.
Note: This is a substrate RNA for the Tobacco ringspot virus satellite RNA Hairpin Ribozyme (Cisterna catalog: CR92). It is intended to be used in conjunction with the ribozyme for cleavage analysis.
1) Hegg, L.A. & Fedor, M.J. (1995). Kinetics and thermodynamics of intermolecular catalysis by hairpin ribozymes. Biochemistry 34(48):15813–15828
2) Fedor, M.J. (2000). Structure and function of the hairpin ribozyme. J Mol Biol 297(2):269–291
3) Cai, Z. & Tinoco, I. (1996). Solution structure of loop A from the hairpin ribozyme from tobacco ringspot virus satellite. Biochemistry 35(19):6026–6036
4) Zhuang, X. et al. (2002). Correlating structural dynamics and function in single ribozyme molecules. Science 296(5572):1473–1476
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