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Recording Temporal Signals with Minutes Resolution Using Enzymatic DNA Synthesis

机译:使用酶DNA合成用分钟分辨率录制时间信号

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摘要

Employing DNA as a high-density data storage medium has paved the way for next-generation digital storage and biosensing technologies. However, the multipart architecture of current DNA-based recording techniques renders them inherently slow and incapable of recording fluctuating signals with subhour frequencies. To address this limitation, we developed a simplified system employing a single enzyme, terminal deoxynucleotidyl transferase (TdT), to transduce environmental signals into DNA. TdT adds nucleotides to the 3'-ends of single-stranded DNA (ssDNA) in a template-independent manner, selecting bases according to inherent preferences and environmental conditions. By characterizing TdT nucleotide selectivity under different conditions, we show that TdT can encode various physiologically relevant signals such as Co~(2+), Ca~(2+), and Zn~(2+) concentrations and temperature changes in vitro. Further, by considering the average rate of nucleotide incorporation, we show that the resulting ssDNA functions as a molecular ticker tape. With this method we accurately encode a temporal record of fluctuations in Co~(2+) concentration to within 1 min over a 60 min period. Finally, we engineer TdT to allosterically turn off in the presence of a physiologically relevant concentration of calcium. We use this engineered TdT in concert with a reference TdT to develop a two-polymerase system capable of recording a single-step change in the Ca~(2+) signal to within 1 min over a 60 min period. This work expands the repertoire of DNA-based recording techniques by developing a novel DNA synthesis-based system that can record temporal environmental signals into DNA with a resolution of minutes.
机译:使用DNA作为高密度数据存储介质已经为下一代数字存储和生物传感技术铺平了道路。然而,当前基于DNA的记录技术的多部分架构使它们具有固有的慢速且无法与子频率记录波动信号。为了解决这些限制,我们开发了一种使用单一酶,末端脱氧核苷酸转移酶(TDT)的简化系统,以将环境信号转化为DNA。 TDT以与模板 - 独立的方式将核苷酸添加到单链DNA(SSDNA)的3末端,根据固有的偏好和环境条件选择碱基。通过在不同条件下表征TDT核苷酸选择性,我们表明TDT可以编码各种生理学相关信号,例如CO〜(2+),Ca〜(2+)和Zn〜(2+)浓度和温度变化。此外,通过考虑核苷酸掺入的平均速率,我们表明所得的SSDNA作为分子胶带。通过这种方法,我们将Co〜(2+)浓度的颞记录精确地编码在60分钟内1分钟内。最后,我们在生理相关的钙的存在下,在存在生理相关的浓度的情况下,我们将TDT设计成变色。我们在音乐会中使用该工程TDT与参考TDT一起开发一种能够在60分钟内在1分钟内记录CA〜(2+)信号的单步变化的两种聚合酶系统。这项工作通过开发基于新型DNA合成的系统,扩展了基于DNA的记录技术的再购,该系统可以通过分辨率将时间环境信号记录到DNA中。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2021年第40期|16630-16640|共11页
  • 作者单位

    Department of Chemical and Biological Engineering Northwestern University Evanston Illinois 60208 United States Mitolab Cambridge Massachusetts 02139 United States;

    Department of Chemical and Biological Engineering Northwestern University Evanston Illinois 60208 United States;

    Department of Chemical and Biological Engineering Northwestern University Evanston Illinois 60208 United States;

    Center for Theoretical Neuroscience Columbia University New York New York 10027 United States;

    Department of Biomedical Engineering Center for Epigenetics Johns Hopkins School of Medicine Baltimore Maryland 21205 United States;

    Department of Brain and Cognitive Sciences Massachusetts Institute of Technology Cambridge Massachusetts 02139 United States McGovern Institute Massachusetts Institute of Technology Cambridge Massachusetts 02139 United States Howard Hughes Medical Institute Department of Neurobiology Harvard Medical School Boston Massachusetts 02115 United States;

    Department of Biomedical Engineering Center for Epigenetics Johns Hopkins School of Medicine Baltimore Maryland 21205 United States;

    Department of Neuroscience University of Pennsylvania Philadelphia Pennsylvania 19104 United States;

    Department of Chemical and Biological Engineering Northwestern University Evanston Illinois 60208 United States;

  • 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);
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  • 正文语种 eng
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