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An Ontology for Facilitating Discussion of Catalytic Strategies of RNA-Cleaving Enzymes

机译:促进RNA切割酶催化策略探讨的本体论

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摘要

A predictive understanding of the mechanisms of RNA cleavage is important for the design of emerging technology built from biological and synthetic molecules that have promise for new biochemical and medicinal applications. Over the past 15 years, RNA cleavage reactions involving 2'-O-transphosphorylation have been discussed using a simplified framework introduced by Breaker that consists of four fundamental catalytic strategies (designated alpha, beta, gamma, and delta) that contribute to rate enhancement. As more detailed mechanistic data emerge, there is need for the framework to evolve and keep pace. We develop an ontology for discussion of strategies of enzymes that catalyze RNA cleavage via 2'-O-transphosphorylation that stratifies Breaker's framework into primary (1 degrees), secondary (2 degrees), and tertiary (3 degrees) contributions to enable more precise interpretation of mechanism in the context of structure and bonding. Further, we point out instances where atomic-level changes give rise to changes in more than one catalytic contribution, a phenomenon we refer to as "functional blurring". We hope that this ontology will help clarify our conversations and pave the path forward toward a consensus view of these fundamental and fascinating mechanisms. The insight gained will deepen our understanding of RNA cleavage reactions catalyzed by natural protein and RNA enzymes, as well as aid in the design of new engineered DNA and synthetic enzymes.
机译:对RNA裂解机制的预测理解对于从生物和合成分子建造的新兴技术设计具有承诺的新兴技术的设计是重要的。在过去的15年中,使用由断路器引入的简化框架讨论了涉及2'-O-转渗磷酸化的RNA切割反应,该骨架由有助于提高速率增强的四种基本催化策略(指定α,β,γ和Δ)。随着更详细的机制数据出现,需要框架来发展并保持速度。我们开发了一种本体论,用于讨论通过2'-O-转磷酸化催化RNA切割的酶的策略,将破碎器的骨架分为原发性(1度),次级(2度)和第三级(3度)贡献,以实现更精确的解释结构与粘接背景下的机制。此外,我们指出了原子水平变化导致多于一个催化贡献的变化的情况,我们称为“功能模糊”的现象。我们希望这种本体论能够帮助澄清我们的谈话,并铺平了对这些基本和迷人机制的共识看法的向前铺平道路。所获得的洞察力将深化我们对天然蛋白质和RNA酶催化的RNA切割反应的理解,以及辅助新工程化DNA和合成酶的设计。

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  • 来源
    《ACS Chemical Biology》 |2019年第6期|共9页
  • 作者单位

    Penn State Univ Dept Chem Ctr RNA Mol Biol University Pk PA 16802 USA;

    Univ Florida Dept Chem Gainesville FL 32611 USA;

    Univ Chicago Dept Chem 5735 S Ellis Ave Chicago IL 60637 USA;

    Rutgers State Univ Lab Biomol Simulat Res Inst Quantitat Biomed Dept Chem &

    Chem Biol Piscataway NJ 08854 USA;

    Rutgers State Univ Lab Biomol Simulat Res Inst Quantitat Biomed Dept Chem &

    Chem Biol Piscataway NJ 08854 USA;

    Rutgers State Univ Lab Biomol Simulat Res Inst Quantitat Biomed Dept Chem &

    Chem Biol Piscataway NJ 08854 USA;

    Rutgers State Univ Lab Biomol Simulat Res Inst Quantitat Biomed Dept Chem &

    Chem Biol Piscataway NJ 08854 USA;

    Rutgers State Univ Lab Biomol Simulat Res Inst Quantitat Biomed Dept Chem &

    Chem Biol Piscataway NJ 08854 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

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