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Exploring the Complex Folding Kinetics of RNA Hairpins: I. General Folding Kinetics Analysis

机译:探索RNA发夹的复杂折叠动力学:I.通用折叠动力学分析

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摘要

Depending on the nucleotide sequence, the temperature, and other conditions, RNA hairpin-folding kinetics can be very complex. The complexity with a wide range of cooperative and noncooperative kinetic behaviors arises from the interplay between the formation of the loops, the disruption of the misfolded states, and the formation of the rate-limiting base stacks. With a rate constant model and a kinetic-cluster theory, we explore the broad landscape for RNA hairpin-folding kinetics. The model is validated through direct tests against several experimental measurements. The general kinetic folding mechanisms and the predicted great variety of folding kinetics are directly applicable and quantitatively testable in experiments. The results from this study suggest that 1), previous experimental findings based on the individual hairpins revealed only a small fraction of much broader and more complex RNA hairpin-folding landscapes; 2), even for structures as simple as hairpins, universal folding timescales and pathways do not exist; and 3), to treat the loop size as the sole factor to determine the hairpin-folding rate is an oversimplification.
机译:根据核苷酸序列,温度和其他条件,RNA发夹折叠动力学可能非常复杂。具有广泛的合作和非合作动力学行为的复杂性是由环的形成,错折叠状态的破坏和限速基堆的形成之间的相互作用引起的。借助速率常数模型和动力学簇理论,我们探索了RNA发夹折叠动力学的广阔前景。该模型通过针对多个实验测量值的直接测试进行了验证。一般的动力学折叠机理和所预测的多种多样的折叠动力学可直接用于实验中并进行定量测试。这项研究的结果表明:1)先前基于单个发夹的实验结果仅显示了小得多的更广泛且更复杂的RNA发夹折叠态势的一小部分; 2)即使对于像发夹这样简单的结构,也不存在通用的折叠时间尺度和路径;和3),将环的大小视为唯一确定发夹折叠速率的因素过于简单。

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