Solution structure of psi32-modified anticodon stem-loop of Escherichia coli tRNAPhe |
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Authors: | Cabello-Villegas Javier Nikonowicz Edward P |
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Affiliation: | Department of Biochemistry and Cell Biology, Rice University, Houston, TX 77251-1892, USA. |
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Abstract: | Nucleoside base modifications can alter the structures and dynamics of RNA molecules and are important in tRNAs for maintaining translational fidelity and efficiency. The unmodified anticodon stem–loop from Escherichia coli tRNAPhe forms a trinucleotide loop in solution, but Mg2+ and dimethylallyl modification of A37 N6 destabilize the loop-proximal base pairs and increase the mobility of the loop nucleotides. The anticodon arm has three additional modifications, ψ32, ψ39, and A37 C2-thiomethyl. We have used NMR spectroscopy to investigate the structural and dynamical effects of ψ32 on the anticodon stem-loop from E.coli tRNAPhe. The ψ32 modification does not significantly alter the structure of the anticodon stem–loop relative to the unmodified parent molecule. The stem of the RNA molecule includes base pairs ψ32-A38 and U33–A37 and the base of ψ32 stacks between U33 and A31. The glycosidic bond of ψ32 is in the anti configuration and is paired with A38 in a Watson–Crick geometry, unlike residue 32 in most crystal structures of tRNA. The ψ32 modification increases the melting temperature of the stem by ~3.5°C, although the ψ32 and U33 imino resonances are exchange broadened. The results suggest that ψ32 functions to preserve the stem integrity in the presence of additional loop modifications or after reorganization of the loop into a translationally functional conformation. |
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