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无终止子模板独立酶促 DNA 合成用于数字信息存储。

Terminator-free template-independent enzymatic DNA synthesis for digital information storage.

机构信息

Department of Genetics, Harvard Medical School, Boston, 02115, MA, USA.

Wyss Institute for Biologically Inspired Engineering at Harvard University, Boston, 02115, MA, USA.

出版信息

Nat Commun. 2019 Jun 3;10(1):2383. doi: 10.1038/s41467-019-10258-1.

Abstract

DNA is an emerging medium for digital data and its adoption can be accelerated by synthesis processes specialized for storage applications. Here, we describe a de novo enzymatic synthesis strategy designed for data storage which harnesses the template-independent polymerase terminal deoxynucleotidyl transferase (TdT) in kinetically controlled conditions. Information is stored in transitions between non-identical nucleotides of DNA strands. To produce strands representing user-defined content, nucleotide substrates are added iteratively, yielding short homopolymeric extensions whose lengths are controlled by apyrase-mediated substrate degradation. With this scheme, we synthesize DNA strands carrying 144 bits, including addressing, and demonstrate retrieval with streaming nanopore sequencing. We further devise a digital codec to reduce requirements for synthesis accuracy and sequencing coverage, and experimentally show robust data retrieval from imperfectly synthesized strands. This work provides distributive enzymatic synthesis and information-theoretic approaches to advance digital information storage in DNA.

摘要

DNA 是一种新兴的数字数据介质,通过专门用于存储应用的合成工艺可以加速其采用。在这里,我们描述了一种新的酶促合成策略,该策略专为数据存储而设计,利用无模板依赖性的聚合酶末端脱氧核苷酸转移酶(TdT)在动力学控制条件下进行。信息存储在 DNA 链中不同核苷酸之间的转换中。为了生成代表用户定义内容的链,我们迭代地添加核苷酸底物,产生短的均聚物延伸,其长度由无三磷酸腺苷酶介导的底物降解控制。通过这种方案,我们合成了携带 144 位的 DNA 链,包括寻址,并通过流式纳孔测序进行了检索。我们进一步设计了一种数字编码解码器,以降低对合成精度和测序覆盖率的要求,并通过实验证明了从合成不完全的链中稳健地检索数据。这项工作提供了分布式酶促合成和信息论方法,以推进 DNA 中的数字信息存储。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85a8/6546792/dfb5113dfbc5/41467_2019_10258_Fig1_HTML.jpg

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