Charge density of divalent metal cations determines RNA stability

被引:135
作者
Koculi, Eda
Hyeon, Changbong
Thirumalai, D. [1 ]
Woodson, Sarah A.
机构
[1] Univ Maryland, Inst Phys Sci & Technol, Biophys Program, College Pk, MD 20742 USA
[2] Univ Maryland, Dept Biochem & Chem, College Pk, MD 20742 USA
[3] Johns Hopkins Univ, TC Jenkins Dept Biophys, Baltimore, MD 21218 USA
关键词
D O I
10.1021/ja068027r
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
RNA molecules are exquisitely sensitive to the properties of counterions. The folding equilibrium of the Tetrahymena ribozyme is measured by nondenaturing gel electrophoresis in the presence of divalent group IIA metal cations. The stability of the folded ribozyme increases with the charge density (zeta) of the cation. Similar scaling is found when the free energy of the RNA folded in small and large metal cations is measured by urea denaturation. Brownian dynamics simulations of a polyelectrolyte show that the experimental observations can be explained by nonspecific ion-RNA interactions in the absence of site-specific metal chelation. The experimental and simulation results establish that RNA stability is largely determined by a combination of counterion charge and the packing efficiency of condensed cations that depends on the excluded volume of the cations.
引用
收藏
页码:2676 / 2682
页数:7
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