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Trapped water molecules are essential to structural dynamics and function of a ribozyme
- Source :
- Proceedings of the National Academy of Sciences. 103:13380-13385
- Publication Year :
- 2006
- Publisher :
- Proceedings of the National Academy of Sciences, 2006.
-
Abstract
- Ribozymes are catalytically competent examples of highly structured noncoding RNAs, which are ubiquitous in the processing and regulation of genetic information. Combining explicit-solvent molecular dynamics simulation and single molecule fluorescence spectroscopy approaches, we find that a ribozyme from a subviral plant pathogen exhibits a coupled hydrogen bonding network that communicates dynamic structural rearrangements throughout the catalytic core in response to site-specific chemical modification. Trapped long-residency water molecules are critical for this network and only occasionally exchange with bulk solvent as they pass through a breathing interdomain base stack. These highly structured water molecules line up in a string that may potentially also be involved in specific base catalysis. Our observations suggest important, still underappreciated roles for specifically bound water molecules in the structural dynamics and function of noncoding RNAs.
- Subjects :
- Models, Molecular
Cations, Divalent
Base pair
Static Electricity
Catalysis
Molecular dynamics
Catalytic Domain
Fluorescence Resonance Energy Transfer
RNA Precursors
Molecule
Bound water
Computer Simulation
Magnesium
RNA, Catalytic
Base Pairing
Multidisciplinary
Base Sequence
biology
Chemistry
Ribozyme
Water
Hydrogen Bonding
Biological Sciences
Models, Theoretical
Single-molecule experiment
Kinetics
Spectrometry, Fluorescence
Förster resonance energy transfer
Biochemistry
Mutation
Solvents
biology.protein
Biophysics
Nucleic Acid Conformation
RNA, Viral
Protons
Hairpin ribozyme
Subjects
Details
- ISSN :
- 10916490 and 00278424
- Volume :
- 103
- Database :
- OpenAIRE
- Journal :
- Proceedings of the National Academy of Sciences
- Accession number :
- edsair.doi.dedup.....a5508c181ab7d6c2c148a1eb213b4f88
- Full Text :
- https://doi.org/10.1073/pnas.0605090103