The fastest global events in RNA folding: Electrostatic relaxation and tertiary collapse of the tetrahymena ribozyme

被引:111
作者
Das, R
Kwok, LW
Millett, IS
Bai, Y
Mills, TT
Jacob, J
Maskel, GS
Seifert, S
Mochrie, SGJ
Thiyagarajan, P
Doniach, S
Pollack, L
Herschlag, D
机构
[1] Argonne Natl Lab, Div Chem, Argonne, IL 60439 USA
[2] Stanford Univ, Dept Phys, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Biochem, Sch Med, Beckman Ctr, Stanford, CA 94305 USA
[4] Cornell Univ, Sch Appl & Engn Phys, Ithaca, NY 14853 USA
[5] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[6] Stanford Univ, Biophys Program, Stanford, CA 94305 USA
[7] Univ Chicago, Dept Biochem & Mol Biol, Chicago, IL 60637 USA
[8] Yale Univ, Dept Phys, New Haven, CT 06520 USA
关键词
RNA folding; time-resolved small-angle X-ray scattering; molten globule; electrostatic relaxation; burst phase;
D O I
10.1016/S0022-2836(03)00854-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Large RNAs can collapse into compact conformations well before the stable formation of the tertiary contacts that define their final folds. This study identifies likely physical mechanisms driving these early compaction events in RNA folding. We have employed time-resolved small-angle X-ray scattering to monitor the fastest global shape changes of the Tetrahymena ribozyme under different ionic conditions and with RNA mutations that remove long-range tertiary contacts. A partial collapse in each of the folding time-courses occurs within tens of milliseconds with either monovalent or divalent cations. Combined with comparison to predictions from structural models, this observation suggests a relaxation of the RNA to a more compact but denatured conformational ensemble in response to enhanced electrostatic screening at higher ionic concentrations. Further, the results provide evidence against counterion-correlation-mediated attraction between RNA double helices, a recently proposed model for early collapse. A previous study revealed a second 100 ms phase of collapse to a globular state. Surprisingly, we find that progression to this second early folding intermediate requires RNA sequence motifs that eventually mediate native long-range tertiary interactions, even though these regions of the RNA were observed to be solvent-accessible in previous footprinting studies under similar conditions. These results help delineate an analogy between the early conformational changes in RNA folding and the "burst phase" changes and molten globule formation in protein folding. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:311 / 319
页数:9
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