Unknotting RNA: A method to resolve computational artifacts.

IF 3.6 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS PLoS Computational Biology Pub Date : 2025-03-20 eCollection Date: 2025-03-01 DOI:10.1371/journal.pcbi.1012843
Simón Poblete, Mikolaj Mlynarczyk, Marta Szachniuk
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Abstract

RNA 3D structure prediction often encounters entanglements, computational artifacts that complicate structural models, resulting in their exclusion from further studies despite the potentially accurate prediction of regions outside the entanglement. This study presents a protocol aimed at resolving such issues in RNA models while preserving the overall 3D fold and structural integrity. By employing the SPQR coarse-grained model and short Molecular Dynamics simulations, the protocol imposes energy terms that enable selective modifications to disentangle structures without causing significant distortions. The method was validated on 195 entangled RNA models from CASP15 and RNA-Puzzles, successfully resolving over 70% of interlaces and approximately 40% of lassos, with minimal impact on the original geometry but notable improvement in ClashScore. The efficiency of untangling conformations that are unequivocally classified as artifacts is 81%. Certain cases, particularly those involving dense packing of atoms or complex secondary structures, posed challenges that limited the efficiency of the method. In this paper, we present quantitative results from the application of the protocol and discuss examples of both successfully disentangled and unresolved structures. We show a viable approach for refining models previously deemed unsuitable due to topological artifacts.

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解开RNA:一种解决计算伪影的方法。
RNA 3D结构预测经常会遇到纠缠,使结构模型复杂化的计算伪影,导致它们被排除在进一步的研究之外,尽管可能准确预测纠缠之外的区域。本研究提出了一种方案,旨在解决RNA模型中的此类问题,同时保持整体3D折叠和结构完整性。通过采用SPQR粗粒度模型和短分子动力学模拟,该协议施加了能量条款,使选择性修改能够在不造成明显扭曲的情况下解开结构。该方法在来自CASP15和RNA- puzzles的195个纠缠RNA模型上进行了验证,成功地解决了超过70%的交错和大约40%的套索,对原始几何形状的影响最小,但在ClashScore上有显著改善。明确归类为人工制品的构象的解结效率为81%。某些情况下,特别是那些涉及原子密集堆积或复杂二级结构的情况,提出了限制该方法效率的挑战。在本文中,我们给出了该协议应用的定量结果,并讨论了成功解缠和未解缠结构的例子。我们展示了一种可行的方法来细化以前由于拓扑工件而被认为不合适的模型。
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来源期刊
PLoS Computational Biology
PLoS Computational Biology BIOCHEMICAL RESEARCH METHODS-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.10
自引率
4.70%
发文量
820
审稿时长
2.5 months
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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