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利用别构 DNA 发夹编程 DNA 反应网络。

Programming DNA Reaction Networks Using Allosteric DNA Hairpins.

机构信息

Key Laboratory of Advanced Design and Intelligent Computing, Ministry of Education, School of Software Engineering, Dalian University, Dalian 116622, China.

School of Computer Science and Technology, Dalian University of Technology, Dalian 116024, China.

出版信息

Biomolecules. 2023 Mar 5;13(3):481. doi: 10.3390/biom13030481.

DOI:10.3390/biom13030481
PMID:36979416
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10046357/
Abstract

The construction of DNA reaction networks with complex functions using various methods has been an important research topic in recent years. Whether the DNA reaction network can perform complex tasks and be recycled directly affects the performance of the reaction network. Therefore, it is very important to design and implement a DNA reaction network capable of multiple tasks and reversible regulation. In this paper, the hairpin allosteric method was used to complete the assembly task of different functional nucleic acids. In addition, information conversion of the network was realized. In this network, multiple hairpins were assembled into nucleic acid structures with different functions to achieve different output information through the cyclic use of trigger strands. A method of single-input dual-output information conversion was proposed. Finally, the network with signal amplification and reversible regulation was constructed. In this study, the reversible regulation of different functional nucleic acids in the same network was realized, which shows the potential of this network in terms of programmability and provides new ideas for constructing complex and multifunctional DNA reaction networks.

摘要

近年来,使用各种方法构建具有复杂功能的 DNA 反应网络一直是一个重要的研究课题。DNA 反应网络是否能够执行复杂任务并直接回收,直接影响反应网络的性能。因此,设计和实现能够进行多项任务和可逆调控的 DNA 反应网络非常重要。在本文中,我们使用发夹变构的方法完成了不同功能的核酸的组装任务。此外,我们还实现了网络的信息转换。在这个网络中,多个发夹通过循环使用触发链组装成具有不同功能的核酸结构,从而通过不同的触发链实现不同的输出信息。提出了一种单输入双输出的信息转换方法。最后,构建了具有信号放大和可逆调控功能的网络。在这项研究中,我们在同一个网络中实现了不同功能的核酸的可逆调控,这表明该网络在可编程性方面具有潜力,为构建复杂多功能的 DNA 反应网络提供了新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c33/10046357/1e62241f39de/biomolecules-13-00481-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c33/10046357/7b47a0ace34b/biomolecules-13-00481-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c33/10046357/5bfecb63072e/biomolecules-13-00481-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c33/10046357/a13f2b43cec5/biomolecules-13-00481-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c33/10046357/f0791cb5ed5b/biomolecules-13-00481-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c33/10046357/8925ce691857/biomolecules-13-00481-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c33/10046357/1e62241f39de/biomolecules-13-00481-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c33/10046357/7b47a0ace34b/biomolecules-13-00481-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c33/10046357/5bfecb63072e/biomolecules-13-00481-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c33/10046357/a13f2b43cec5/biomolecules-13-00481-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c33/10046357/f0791cb5ed5b/biomolecules-13-00481-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c33/10046357/8925ce691857/biomolecules-13-00481-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c33/10046357/1e62241f39de/biomolecules-13-00481-g006.jpg

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Brief Bioinform. 2023 Jan 19;24(1). doi: 10.1093/bib/bbac524.
2
FMG: An observable DNA storage coding method based on frequency matrix game graphs.FMG:基于频域矩阵博弈图的可观察 DNA 存储编码方法。
Comput Biol Med. 2022 Dec;151(Pt A):106269. doi: 10.1016/j.compbiomed.2022.106269. Epub 2022 Nov 3.
3
Improved Bare Bones Particle Swarm Optimization for DNA Sequence Design.
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IEEE Trans Nanobioscience. 2023 Jul;22(3):603-613. doi: 10.1109/TNB.2022.3220795. Epub 2023 Jun 29.
4
TripDesign: A DNA Triplex Design Approach Based on Interaction Forces.基于相互作用力的 DNA 三链体设计方法(TripDesign)
J Phys Chem B. 2022 Nov 3;126(43):8708-8719. doi: 10.1021/acs.jpcb.2c05611. Epub 2022 Oct 19.
5
Cationic Copolymer-Augmented DNA Hybridization Chain Reaction.阳离子共聚物增强的 DNA 杂交链式反应。
ACS Appl Mater Interfaces. 2022 Aug 31;14(34):39396-39403. doi: 10.1021/acsami.2c11548. Epub 2022 Aug 16.
6
Simultaneous Visualization of Dual Intercellular Signal Transductions via SERS Imaging of Membrane Proteins Dimerization on Single Cells.通过对单个细胞上膜蛋白二聚化的 SERS 成像实现双重细胞内信号转导的同时可视化。
ACS Nano. 2022 Sep 27;16(9):14055-14065. doi: 10.1021/acsnano.2c03914. Epub 2022 Aug 15.
7
On-Site Non-enzymatic Orthogonal Activation of a Catalytic DNA Circuit for Self-Reinforced In Vivo MicroRNA Imaging.现场非酶正交激活催化 DNA 电路用于自我增强的体内 microRNA 成像。
Angew Chem Int Ed Engl. 2022 Nov 7;61(45):e202206529. doi: 10.1002/anie.202206529. Epub 2022 Aug 29.
8
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9
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Langmuir. 2022 Apr 26;38(16):4870-4878. doi: 10.1021/acs.langmuir.2c00043. Epub 2022 Apr 14.
10
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Nanoscale. 2022 May 5;14(17):6585-6599. doi: 10.1039/d1nr06861j.