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模块化 CRISPR/Cas12a 协同激活平台,用于检测和逻辑运算。

Modular CRISPR/Cas12a synergistic activation platform for detection and logic operations.

机构信息

School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.

Department of Oncology, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.

出版信息

Nucleic Acids Res. 2024 Jul 8;52(12):7384-7396. doi: 10.1093/nar/gkae470.

DOI:10.1093/nar/gkae470
PMID:38828769
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11229313/
Abstract

The revolutionary technology of CRISPR/Cas has reshaped the landscape of molecular biology and molecular engineering. This tool is of interest to researchers in multiple fields, including molecular diagnostics, molecular biochemistry circuits, and information storage. As CRISPR/Cas spreads to more niche areas, new application scenarios and requirements emerge. Developing programmability and compatibility of CRISPR/Cas becomes a critical issue in the new phase. Here, we report a redundancy-based modular CRISPR/Cas12a synergistic activation platform (MCSAP). The position, length, and concentration of the redundancy in the split DNA activators can finely regulate the activity of Cas12a. With the redundant structure as an interface, MCSAP serves as a modular plug-in to seamlessly integrate with the upstream molecular network. MCSAP successfully performs three different tasks: nucleic acid detection, enzyme detection, and logic operation. MCSAP can work as an effector for different molecular networks because of its compatibility and programmability. Our platform provides powerful yet easy-to-use tools and strategies for the fields of DNA nanotechnology, molecular engineering, and molecular biology.

摘要

CRISPR/Cas 的革命性技术改变了分子生物学和分子工程的格局。这一工具引起了包括分子诊断、分子生化电路和信息存储在内的多个领域研究人员的兴趣。随着 CRISPR/Cas 技术扩展到更多的专业领域,新的应用场景和需求不断涌现。开发 CRISPR/Cas 的可编程性和兼容性成为新阶段的关键问题。在这里,我们报告了一种基于冗余的模块化 CRISPR/Cas12a 协同激活平台(MCSAP)。在分割 DNA 激活子中的冗余位置、长度和浓度可以精细调节 Cas12a 的活性。MCSAP 以冗余结构作为接口,作为一个模块化插件,可以与上游分子网络无缝集成。MCSAP 成功执行了三种不同的任务:核酸检测、酶检测和逻辑运算。由于其兼容性和可编程性,MCSAP 可以作为不同分子网络的效应器。我们的平台为 DNA 纳米技术、分子工程和分子生物学领域提供了强大而易用的工具和策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d8/11229313/a7aa94b2faa7/gkae470fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d8/11229313/119fecba599b/gkae470figgra1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d8/11229313/54e7037ecfac/gkae470fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d8/11229313/d9747826515e/gkae470fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d8/11229313/8a3a28dca09a/gkae470fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d8/11229313/5d49b037f244/gkae470fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d8/11229313/4e55cd56062d/gkae470fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d8/11229313/a7aa94b2faa7/gkae470fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d8/11229313/119fecba599b/gkae470figgra1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d8/11229313/54e7037ecfac/gkae470fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d8/11229313/d9747826515e/gkae470fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d8/11229313/8a3a28dca09a/gkae470fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d8/11229313/5d49b037f244/gkae470fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d8/11229313/4e55cd56062d/gkae470fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d8/11229313/a7aa94b2faa7/gkae470fig6.jpg

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ACS Nano. 2024 Jan 23;18(3):2184-2194. doi: 10.1021/acsnano.3c09506. Epub 2024 Jan 9.
3
Gene point mutation information translation and detection: Leveraging single base extension and CRISPR/Cas12a.
Adv Sci (Weinh). 2025 Aug;12(32):e05793. doi: 10.1002/advs.202505793. Epub 2025 Jun 19.
4
Exploring the effect of activator topology on CRISPR-Cas12a trans-cleavage activity.探索激活剂拓扑结构对CRISPR-Cas12a反式切割活性的影响。
Nucleic Acids Res. 2025 Apr 22;53(8). doi: 10.1093/nar/gkaf311.
5
Regulation of CRISPR trans-cleavage activity by an overhanging activator.通过突出的激活剂对CRISPR反式切割活性的调控
Nucleic Acids Res. 2025 Feb 8;53(4). doi: 10.1093/nar/gkaf117.
6
Direct repeat region 3' end modifications regulate Cas12a activity and expand its applications.直接重复序列区域3'末端修饰调控Cas12a活性并拓展其应用。
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7
Engineering stimuli-responsive CRISPR-Cas systems for versatile biosensing.构建用于多功能生物传感的刺激响应型CRISPR-Cas系统。
Anal Bioanal Chem. 2025 Apr;417(9):1699-1711. doi: 10.1007/s00216-024-05678-y. Epub 2024 Nov 27.
基因点突变信息的翻译和检测:利用单碱基延伸和 CRISPR/Cas12a。
Biosens Bioelectron. 2024 Mar 1;247:115936. doi: 10.1016/j.bios.2023.115936. Epub 2023 Dec 20.
4
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Angew Chem Int Ed Engl. 2023 Dec 4;62(49):e202314386. doi: 10.1002/anie.202314386. Epub 2023 Oct 31.
5
Molecular tumour boards - current and future considerations for precision oncology.分子肿瘤委员会——精准肿瘤学的当前和未来考量。
Nat Rev Clin Oncol. 2023 Dec;20(12):843-863. doi: 10.1038/s41571-023-00824-4. Epub 2023 Oct 16.
6
Digital data storage on DNA tape using CRISPR base editors.基于 CRISPR 碱基编辑器的 DNA 带数字数据存储。
Nat Commun. 2023 Oct 13;14(1):6472. doi: 10.1038/s41467-023-42223-4.
7
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Nucleic Acids Res. 2023 Oct 27;51(19):10795-10807. doi: 10.1093/nar/gkad748.
8
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Nat Commun. 2023 Sep 5;14(1):5409. doi: 10.1038/s41467-023-41006-1.
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J Am Chem Soc. 2023 Sep 20;145(37):20412-20421. doi: 10.1021/jacs.3c05879. Epub 2023 Aug 31.
10
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Anal Chem. 2023 Aug 15;95(32):12169-12176. doi: 10.1021/acs.analchem.3c02471. Epub 2023 Aug 2.