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Molecular crowding effect on metal ion binding properties of the hammerhead ribozyme
Author(s) -
Shuichi Nakano,
Yuichi Kitagawa,
Hisae Karimata,
Naoki Sugimoto
Publication year - 2008
Publication title -
nucleic acids symposium series
Language(s) - English
Resource type - Journals
eISSN - 1746-8272
pISSN - 0261-3166
DOI - 10.1093/nass/nrn263
Subject(s) - hammerhead ribozyme , chemistry , ribozyme , metal , metal ions in aqueous solution , cooperativity , ethylene glycol , divalent , rna , inorganic chemistry , crystallography , biochemistry , organic chemistry , gene
Although metal ion is essential for the DNA and RNA folding, there are a limited number of reports describing the influence of molecular environments on the metal ion binding. Here, we investigated the binding properties of Mg(2+) and Na(+) toward the hammerhead ribozyme in the presence of PEG [poly(ethylene glycol)] as a cosolute that changes the solvent property of the reaction. PEG8000 (PEG with the average molecular weight of 8000) increased the reaction rate at lower Mg(2+) concentrations but not at higher concentrations. We also found that PEG8000 unchanged the number of Mg(2+) bound while the binding cooperativity of Na(+) in the reaction without divalent metal ion was altered. The change of Na(+) condensation by cosolute has also been reported for diffusely bound Na(+) to Watson-Crick base pairs. It is thus supposed that diffusely bound Na(+) stabilizes the ribozyme active form in the absence of divalent metal ion. This study provides insights into the RNA-metal ion interaction and the hammerhead ribozyme activity under the molecular crowding condition occurred in a cell and on biosensor devices.

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