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一种用于序列选择性结合、下拉和释放 DNA 靶标的智能聚合物。

A smart polymer for sequence-selective binding, pulldown, and release of DNA targets.

机构信息

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA, USA.

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

出版信息

Commun Biol. 2020 Jul 10;3(1):369. doi: 10.1038/s42003-020-1082-2.


DOI:10.1038/s42003-020-1082-2
PMID:32651444
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7351716/
Abstract

Selective isolation of DNA is crucial for applications in biology, bionanotechnology, clinical diagnostics and forensics. We herein report a smart methanol-responsive polymer (MeRPy) that can be programmed to bind and separate single- as well as double-stranded DNA targets. Captured targets are quickly isolated and released back into solution by denaturation (sequence-agnostic) or toehold-mediated strand displacement (sequence-selective). The latter mode allows 99.8% efficient removal of unwanted sequences and 79% recovery of highly pure target sequences. We applied MeRPy for the depletion of insulin, glucagon, and transthyretin cDNA from clinical next-generation sequencing (NGS) libraries. This step improved the data quality for low-abundance transcripts in expression profiles of pancreatic tissues. Its low cost, scalability, high stability and ease of use make MeRPy suitable for diverse applications in research and clinical laboratories, including enhancement of NGS libraries, extraction of DNA from biological samples, preparative-scale DNA isolations, and sorting of DNA-labeled non-nucleic acid targets.

摘要

DNA 的选择性分离对于生物学、生物纳米技术、临床诊断和法医学等领域的应用至关重要。本文报道了一种智能甲醇响应聚合物(MeRPy),它可以被编程用于结合和分离单链和双链 DNA 靶标。通过变性(序列无关)或引发链置换(序列选择性),捕获的靶标可以快速分离并重新释放到溶液中。后一种模式可以高效地去除不需要的序列,而 79%的高纯度靶序列可以被回收。我们将 MeRPy 应用于从临床下一代测序(NGS)文库中去除胰岛素、胰高血糖素和转甲状腺素 cDNA。这一步骤提高了胰腺组织表达谱中低丰度转录本的数据质量。MeRPy 具有成本低、可扩展性、高稳定性和易于使用等特点,适用于研究和临床实验室的多种应用,包括增强 NGS 文库、从生物样本中提取 DNA、制备规模的 DNA 分离以及 DNA 标记的非核酸靶标的分选。

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引用本文的文献

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Y-switch: a spring-loaded synthetic gene switch for robust DNA/RNA signal amplification and detection.

Nucleic Acids Res. 2024-9-23

[2]
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[3]
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[4]
Mini review: Enzyme-based DNA synthesis and selective retrieval for data storage.

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[5]
Rapid in vitro production of single-stranded DNA.

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本文引用的文献

[1]
Rapid in vitro production of single-stranded DNA.

Nucleic Acids Res. 2019-12-16

[2]
Evaluation of protocols for rRNA depletion-based RNA sequencing of nanogram inputs of mammalian total RNA.

PLoS One. 2019-10-31

[3]
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Nucleic Acids Res. 2019-2-28

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Simultaneous and stoichiometric purification of hundreds of oligonucleotides.

Nat Commun. 2018-6-25

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Nucleic Acids Res. 2018-4-6

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Nat Cell Biol. 2018-2-19

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Nature. 2017-12-6

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Selective Nascent Polymer Catch-and-Release Enables Scalable Isolation of Multi-Kilobase Single-Stranded DNA.

Angew Chem Int Ed Engl. 2017-12-18

[9]
Systems biology of the IMIDIA biobank from organ donors and pancreatectomised patients defines a novel transcriptomic signature of islets from individuals with type 2 diabetes.

Diabetologia. 2017-11-28

[10]
Is the $1000 Genome as Near as We Think? A Cost Analysis of Next-Generation Sequencing.

Clin Chem. 2016-9-14

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