期刊论文详细信息
JOURNAL OF MOLECULAR BIOLOGY 卷:393
Metal Ion Dependence of Cooperative Collapse Transitions in RNA
Article
Moghaddam, Sarvin1  Caliskan, Gokhan2  Chauhan, Seema3  Hyeon, Changbong4  Briber, R. M.1  Thirumalai, D.5  Woodson, Sarah A.2 
[1] Univ Maryland, Dept Mat Sci & Engn, College Pk, MD 20472 USA
[2] Johns Hopkins Univ, TC Jenkins Dept Biophys, Baltimore, MD 21218 USA
[3] Johns Hopkins Univ, Dept Chem, Baltimore, MD 21218 USA
[4] Chung Ang Univ, Dept Chem, Seoul 156756, South Korea
[5] Univ Maryland, Biophys Program, Inst Phys Sci & Technol, College Pk, MD 20472 USA
关键词: RNA folding;    SAXS;    counterion;    ribozyme;    singular value decomposition;   
DOI  :  10.1016/j.jmb.2009.08.044
来源: Elsevier
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【 摘 要 】

Positively charged counterions drive RNA molecules into compact configurations that lead to their biologically active structures. To understand how the valence and size of the cations influences the collapse transition in RNA, small-angle X-ray scattering was used to follow the decrease in the radius of gyration (R-g) of the Azoarcus and Tetrahymena ribozymes in different cations. Small, multivalent cations induced the collapse of both ribozymes more efficiently than did monovalent ions. Thus, the cooperativity of the collapse transition depends on the counterion charge density. Singular value decomposition of the scattering curves showed that folding of the smaller and more thermostable Azoarcus ribozyme is well described by two components, whereas collapse of the larger Tetrahymena ribozyme involves at least one intermediate. The ion-dependent persistence length, extracted from the distance distribution of the scattering vectors, shows that the Azoarcus ribozyme is less flexible at the midpoint of transition in low-charge-density ions than in high-charge-density ions. We conclude that the formation of sequence-specific tertiary interactions in the Azoarcus ribozyme overlaps with neutralization of the phosphate charge, while tertiary folding of the Tetrahymena ribozyme requires additional counterions. Thus, the stability of the RNA structure determines its sensitivity to the valence and size of the counterions. (c) 2009 Elsevier Ltd. All rights reserved.

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