Establishing the catalytic and regulatory mechanism of RNA-based machineries

IF 16.8 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Jure Bori?ek, Jana Aupi?, Alessandra Magistrato
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引用次数: 5

Abstract

Ribonucleoprotein (RNP)-machineries are comprised of intricate networks of long noncoding RNAs and proteins that allow them to actively participate in transcription, RNA processing, and translation. RNP-machineries thus play vital roles in gene expression and regulation. Recent advances in cryo-EM techniques provided a wealth of near-atomic-level resolution structures setting the basis for understanding how these fascinating multiscale complexes exert their diverse roles. However, these structures represent only isolated snapshots of the plastic and highly dynamic RNP-machineries and are thus insufficient to comprehensively assess their multifaceted mechanisms. In this review, we discuss the role and merit of all-atom simulations in disentangling the mechanism of eukaryotic RNA-based machineries responsible for RNA processing. We showcase how all-atom simulations can capture their large-scale functional movements, trace the signaling pathways that are at the root of their massive conformational remodeling, explain recognition mechanisms of specific RNA sequences, and, lastly, unravel the chemical mechanisms underlying the formation of functional RNA strands. Finally, we review the methodological pitfalls and outline future challenges in modeling key functional aspects of these large molecular engines with all-atom simulations. In addition to providing insights into the most basic processes that govern all forms of life, in-depth mechanistic comprehension of RNP-machineries offers a foundation for developing innovative therapeutic strategies against the variety of human diseases linked to deregulated RNA metabolism.

This article is categorized under:

Abstract Image

建立基于rna的机制的催化调控机制
核糖核蛋白(RNP)机制由长链非编码RNA和蛋白质的复杂网络组成,这些网络允许它们积极参与转录、RNA加工和翻译。因此,rnp机制在基因表达和调控中起着至关重要的作用。低温电镜技术的最新进展提供了丰富的近原子水平分辨率结构,为理解这些迷人的多尺度复合物如何发挥其不同作用奠定了基础。然而,这些结构仅代表了塑性和高动态rnp机制的孤立快照,因此不足以全面评估其多方面机制。在这篇综述中,我们讨论了全原子模拟在解开真核生物RNA加工机制中的作用和优点。我们展示了全原子模拟如何捕获它们的大规模功能运动,追踪它们大规模构象重塑的根本信号通路,解释特定RNA序列的识别机制,最后揭示功能性RNA链形成的化学机制。最后,我们回顾了方法上的缺陷,并概述了用全原子模拟模拟这些大分子发动机的关键功能方面的未来挑战。除了提供对支配所有生命形式的最基本过程的见解之外,对rnp机制的深入机制理解为开发针对与RNA代谢失调相关的各种人类疾病的创新治疗策略提供了基础。本文分类如下:
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来源期刊
Wiley Interdisciplinary Reviews: Computational Molecular Science
Wiley Interdisciplinary Reviews: Computational Molecular Science CHEMISTRY, MULTIDISCIPLINARY-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
28.90
自引率
1.80%
发文量
52
审稿时长
6-12 weeks
期刊介绍: Computational molecular sciences harness the power of rigorous chemical and physical theories, employing computer-based modeling, specialized hardware, software development, algorithm design, and database management to explore and illuminate every facet of molecular sciences. These interdisciplinary approaches form a bridge between chemistry, biology, and materials sciences, establishing connections with adjacent application-driven fields in both chemistry and biology. WIREs Computational Molecular Science stands as a platform to comprehensively review and spotlight research from these dynamic and interconnected fields.
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