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Constrained Multistate Sequence Design for Nucleic Acid Reaction Pathway Engineering

机译:核酸反应途径工程的约束多态序列设计

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摘要

We describe a framework for designing the sequences of multiple nucleic acid strands intended to hybridize in solution via a prescribed reaction pathway. Sequence design is formulated as a multistate optimization problem using a set of target test tubes to represent reactant, intermediate, and product states of the system, as well as to model crosstalk between components. Each target test tube contains a set of desired "on-target" complexes, each with a target secondary structure and target concentration, and a set of undesired "off-target" complexes, each with vanishing target concentration. Optimization of the equilibrium ensemble properties of the target test tubes implements both a positive design paradigm, explicidy designing for on-pathway elementary steps, and a negative design paradigm, explicidy designing against off-pathway crosstalk Sequence design is performed subject to diverse user-specified sequence constraints including composition constraints, complementarity constraints, pattern prevention constraints, and biological constraints. Constrained multistate sequence design facilitates nucleic acid reaction pathway engineering for diverse applications in molecular programming and synthetic biology. Design jobs can be run online via the NUPACK web application.
机译:我们描述了用于设计旨在通过规定的反应途径在溶液中杂交的多条核酸链的序列的框架。使用一组目标试管来表示系统的反应物,中间物和产物状态,以及对组件之间的串扰进行建模,从而将序列设计表述为多状态优化问题。每个目标试管包含一组所需的“目标上”复合物,每个复合物均具有目标二级结构和目标浓度,以及一组不需要的“目标外”复合物,每个复合物均具有消失的目标浓度。目标试管平衡集合特性的优化既可以实现正向设计范式(针对路途基本步骤的爆炸性设计),也可以实现负向设计范式(针对路径外串扰的爆炸性设计),并根据不同的用户指定进行序列设计序列约束包括组成约束,互补约束,模式预防约束和生物学约束。受限的多态序列设计有助于核酸反应途径的工程设计,以用于分子编程和合成生物学中的各种应用。可以通过NUPACK Web应用程序在线运行设计作业。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2017年第8期|3134-3144|共11页
  • 作者单位

    Division of Biology & Biological Engineering, California Institute of Technology, Pasadena, California 91125, United States;

    Division of Chemistry & Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States;

    Division of Biology & Biological Engineering, California Institute of Technology, Pasadena, California 91125, United States;

    Division of Biology & Biological Engineering, California Institute of Technology, Pasadena, California 91125, United States;

    Division of Biology & Biological Engineering, California Institute of Technology, Pasadena, California 91125, United States,Division of Engineering & Applied Science, California Institute of Technology, Pasadena, California 91125, United States,Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, United Kingdom;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-18 03:07:55

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