Role of metal ions in the tetraloop–receptor complex as analyzed by NMR
- 21 November 2006
- journal article
- Published by Cold Spring Harbor Laboratory in RNA
- Vol. 13 (1) , 76-86
- https://doi.org/10.1261/rna.268307
Abstract
Metal ions are critical for the proper folding of RNA, and the GAAA tetraloop–receptor is necessary for the optimal folding and function of many RNAs. We have used NMR to investigate the role of metal ions in the structure of the tetraloop–receptor in solution. The NMR data indicate native tertiary structure is formed under a wide range of ionic conditions. The lack of conformational adaptation in response to very different ionic conditions argues against a structural role for divalent ions. Nuclear Overhauser effects to cobalt hexammine and paramagnetic relaxation enhancement induced by manganese ions were used to determine the NMR structures of the tetraloop receptor in association with metal ions, providing the first atomic-level view of these interactions in the solution state. Five manganese and two cobalt hexammine ions could be localized to the RNA surface. The locations of the associated metal ions are similar, but not identical to, those of previously determined crystal structures. The sites of association are in general agreement with nonlinear Poisson–Boltzmann calculations of the electrostatic surface, emphasizing the general importance of diffusely associated ions in RNA tertiary structure.Keywords
This publication has 51 references indexed in Scilit:
- Site-directed Spin Labeling Studies Reveal Solution Conformational Changes in a GAAA Tetraloop Receptor upon Mg2+-dependent Docking of a GAAA TetraloopJournal of Molecular Biology, 2005
- RNA Helical Packing in Solution: NMR Structure of a 30kDa GAAA Tetraloop–Receptor ComplexJournal of Molecular Biology, 2005
- Electrostatics of nanosystems: Application to microtubules and the ribosomeProceedings of the National Academy of Sciences, 2001
- Prediction of Sterically Induced Alignment in a Dilute Liquid Crystalline Phase: Aid to Protein Structure Determination by NMRJournal of the American Chemical Society, 2000
- Multiple tertiary interactions involving domain II of group II self-splicing introns 1 1Edited by M. YanivJournal of Molecular Biology, 1997
- Control of Memory Formation Through Regulated Expression of a CaMKII TransgeneScience, 1996
- MOLMOL: A program for display and analysis of macromolecular structuresJournal of Molecular Graphics, 1996
- NMRPipe: A multidimensional spectral processing system based on UNIX pipesJournal of Biomolecular NMR, 1995
- Involvement of a GNRA tetraloop in long-range RNA tertiary interactionsJournal of Molecular Biology, 1994
- Role of Divalent Ions in Folding of tRNAEuropean Journal of Biochemistry, 1977