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Structural parameters affecting the kinetics of RNA hairpin formation

机译:影响RNA发夹形成动力学的结构参数

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There is little experimental knowledge on the sequence dependent rate of hairpin formation in RNA. We have therefore designed RNA sequences that can fold into either of two mutually exclusive hairpins and have determined the ratio of folding of the two conformations, using structure probing. This folding ratio reflects their respective folding rates. Changing one of the two loop sequences from a purine- to a pyrimidine-rich loop did increase its folding rate, which corresponds well with similar observations in DNA hairpins. However, neither changing one of the loops from a regular non-GNRA tetra-loop into a stable GNRA tetra-loop, nor increasing the loop size from 4 to 6 nt did affect the folding rate. The folding kinetics of these RNAs have also been simulated with the program 'Kinfold'. These simulations were in agreement with the experimental results if the additional stabilization energies for stable tetra-loops were not taken into account. Despite the high stability of the stable tetra-loops, they apparently do not affect folding kinetics of these RNA hairpins. These results show that it is possible to experimentally determine relative folding rates of hairpins and to use these data to improve the computer-assisted simulation of the folding kinetics of stem-loop structures.
机译:关于RNA中发夹形成的序列依赖性速率的实验知识很少。因此,我们设计了可折叠成两个互斥的发夹中任一个的RNA序列,并使用结构探测法确定了两个构象的折叠比例。该折叠率反映了它们各自的折叠率。将两个环序列之一从富含嘌呤的环变为富含嘧啶的环确实增加了其折叠率,这与DNA发夹中的类似观察结果非常吻合。但是,将环中的一个从常规非GNRA四环更改为稳定的GNRA四环,或者将环大小从4 nt增加到6 nt都不会影响折叠率。这些RNA的折叠动力学也已经用程序“ Kinfold”进行了模拟。如果不考虑稳定四环的附加稳定能,则这些仿真与实验结果相符。尽管稳定的四环具有很高的稳定性,但它们显然不影响这些RNA发夹的折叠动力学。这些结果表明,可以通过实验确定发夹的相对折叠速率,并使用这些数据来改进茎环结构折叠动力学的计算机辅助模拟。

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