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A Synthetic Light-Driven Substrate Channeling System for Precise Regulation of Enzyme Cascade Activity Based on DNA Origami

机译:基于DNA折纸的精确调控酶级联反应的合成光驱动底物通道系统

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摘要

Substrate channeling, in which a metabolic intermediate is directly passed from one enzyme to the next enzyme in an enzyme cascade, accelerates the processing of metabolites and improves substrate selectivity. Synthetic design and precise control of channeling outside the cellular environment are of significance in areas such as synthetic biology, synthetic chemistry, and biomedicine. In particular, the precise control of synthetic substrate channeling in response to light is highly important, but remains a major challenge. Herein, we develop a photoresponsive molecule-based synthetic substrate channeling system on DNA origami to regulate enzyme cascade activity. The photoresponsive azobenzene molecules introduced into DNA strands enable reversible switching of the position of substrate channeling to selectively activate or inhibit the enzyme cascade activity. Moreover, DNA origami allows precise control of interenzyme distance and swinging range of the swing arm to optimize the regulation efficiency. By combining the accurate and addressable assembly ability of DNA origami and the clean, rapid, and reversible regulation of photoresponsive molecules, this light-driven substrate channeling system is expected to find important applications in synthetic biology and biomedicine.
机译:底物通道化,其中代谢中间体在一个酶级联中直接从一种酶传递到另一种酶,加速了代谢物的加工并提高了底物选择性。在诸如合成生物学,合成化学和生物医学等领域,合成设计和精确控制细胞环境之外的通道非常重要。特别地,对光响应的合成底物通道的精确控制非常重要,但是仍然是主要挑战。在本文中,我们在DNA折纸上开发了基于光响应分子的合成底物通道系统,以调节酶的级联活性。引入DNA链的光响应性偶氮苯分子可实现底物通道位置的可逆转换,从而选择性激活或抑制酶的级联活性。此外,DNA折纸可精确控制酶之间的距离和摆臂的摆动范围,从而优化调节效率。通过将DNA折纸的准确和可寻址的组装能力与对光敏分子的清洁,快速和可逆调节相结合,这种光驱动的底物通道系统有望在合成生物学和生物医学中找到重要的应用。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2018年第28期|8990-8996|共7页
  • 作者单位

    Collaborative Innovation Center of Chemistry for Energy Materials, The MOE Key Laboratory of Spectrochemical Analysis and Instrumentation, State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Chemical Biology, College of Chemistry and Chemical Engineering, Xiamen University;

    Molecular Sciences and Biomedicine Laboratory, State Key Laboratory for Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University;

    Collaborative Innovation Center of Chemistry for Energy Materials, The MOE Key Laboratory of Spectrochemical Analysis and Instrumentation, State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Chemical Biology, College of Chemistry and Chemical Engineering, Xiamen University;

    Collaborative Innovation Center of Chemistry for Energy Materials, The MOE Key Laboratory of Spectrochemical Analysis and Instrumentation, State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Chemical Biology, College of Chemistry and Chemical Engineering, Xiamen University;

    Center for Molecular Design and Biomimetics, Biodesign Institute and School of Molecular Sciences at Arizona State University;

    Center for Molecular Design and Biomimetics, Biodesign Institute and School of Molecular Sciences at Arizona State University;

    Center for Molecular Design and Biomimetics, Biodesign Institute and School of Molecular Sciences at Arizona State University;

    Collaborative Innovation Center of Chemistry for Energy Materials, The MOE Key Laboratory of Spectrochemical Analysis and Instrumentation, State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Chemical Biology, College of Chemistry and Chemical Engineering, Xiamen University,Institute of Molecular Medicine, Renji Hospital, Shanghai Jiao Tong University;

  • 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
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  • 入库时间 2022-08-18 03:07:22

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