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集成模拟:一种高效移码RNA假结的折叠、解折叠和错误折叠

Ensemble simulations: folding, unfolding and misfolding of a high-efficiency frameshifting RNA pseudoknot.

作者信息

Q Nguyen Khai K, Gomez Yessica K, Bakhom Mona, Radcliffe Amethyst, La Phuc, Rochelle Dakota, Lee Ji Won, Sorin Eric J

机构信息

Department of Chemistry & Biochemistry, California State University Long Beach, Long Beach, CA 90840, USA.

Department of Computer Engineering & Computer Science, California State University Long Beach, Long Beach, CA 90840, USA.

出版信息

Nucleic Acids Res. 2017 May 5;45(8):4893-4904. doi: 10.1093/nar/gkx012.

Abstract

Massive all-atom molecular dynamics simulations were conducted across a distributed computing network to study the folding, unfolding, misfolding and conformational plasticity of the high-efficiency frameshifting double mutant of the 26 nt potato leaf roll virus RNA pseudoknot. Our robust sampling, which included over 40 starting structures spanning the spectrum from the extended unfolded state to the native fold, yielded nearly 120 μs of cumulative sampling time. Conformational microstate transitions on the 1.0 ns to 10.0 μs timescales were observed, with post-equilibration sampling providing detailed representations of the conformational free energy landscape and the complex folding mechanism inherent to the pseudoknot motif. Herein, we identify and characterize two alternative native structures, three intermediate states, and numerous misfolded states, the latter of which have not previously been characterized via atomistic simulation techniques. While in line with previous thermodynamics-based models of a general RNA folding mechanism, our observations indicate that stem-strand-sequence-separation may serve as an alternative predictor of the order of stem formation during pseudoknot folding. Our results contradict a model of frameshifting based on structural rigidity and resistance to mechanical unfolding, and instead strongly support more recent studies in which conformational plasticity is identified as a determining factor in frameshifting efficiency.

摘要

通过分布式计算网络进行了大规模全原子分子动力学模拟,以研究26个核苷酸的马铃薯卷叶病毒RNA假结高效移码双突变体的折叠、解折叠、错误折叠和构象可塑性。我们强大的采样包括40多个起始结构,涵盖从伸展未折叠状态到天然折叠状态的范围,累积采样时间接近120微秒。观察到了1.0纳秒到10.0微秒时间尺度上的构象微态转变,平衡后采样提供了构象自由能景观以及假结基序固有的复杂折叠机制的详细表示。在此,我们识别并表征了两种替代天然结构、三种中间状态和许多错误折叠状态,后者以前尚未通过原子模拟技术进行表征。虽然与先前基于热力学的一般RNA折叠机制模型一致,但我们的观察结果表明,茎-链-序列分离可能作为假结折叠过程中茎形成顺序的替代预测指标。我们的结果与基于结构刚性和抗机械解折叠的移码模型相矛盾,反而有力地支持了最近的研究,其中构象可塑性被确定为移码效率的决定因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24b7/5416846/01fb14f68406/gkx012fig1.jpg

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