Nakano Shu-ichi, Kitagawa Yuichi, Karimata Hisae Tateishi, Sugimoto Naoki
Frontier Institute for Biomolecular Engineering Research (FIBER), Konan University, Higashinada-ku, Kobe 658-8501, Japan.
Nucleic Acids Symp Ser (Oxf). 2008(52):519-20. doi: 10.1093/nass/nrn263.
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.
尽管金属离子对于DNA和RNA折叠至关重要,但描述分子环境对金属离子结合影响的报道数量有限。在此,我们研究了在聚乙二醇(PEG)作为共溶质存在的情况下,Mg(2+)和Na(+)与锤头状核酶的结合特性,PEG会改变反应的溶剂性质。聚乙二醇8000(平均分子量为8000的PEG)在较低Mg(2+)浓度下提高了反应速率,但在较高浓度下则没有。我们还发现,聚乙二醇8000在不改变结合的Mg(2+)数量的情况下,却改变了无二价金属离子反应中Na(+)的结合协同性。对于扩散结合到沃森-克里克碱基对的Na(+),也有报道称共溶质会改变其缩合情况。因此推测,在无二价金属离子的情况下,扩散结合的Na(+)会稳定核酶的活性形式。本研究为细胞和生物传感器装置中发生的分子拥挤条件下的RNA-金属离子相互作用及锤头状核酶活性提供了见解。