• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于滤膜的比色法用于基于 CRISPR-Cas12a 的即时检测生物标志物

Filter Membrane-Based Colorimetric Approach for Point-of-Care Detection of Biomarkers Using CRISPR-Cas12a.

机构信息

College of Chemistry, Chemical Engineering and Materials Science, Key Laboratory of Molecular and Nano Probes, Ministry of Education, Collaborative Innovation Center of Functionalized Probes for Chemical Imaging in Universities of Shandong, Institute of Molecular and Nano Science, Shandong Normal University, Jinan 250014, P. R. China.

Laoshan Laboratory, Qingdao 266237, P. R. China.

出版信息

Anal Chem. 2024 Oct 1;96(39):15789-15796. doi: 10.1021/acs.analchem.4c03959. Epub 2024 Sep 23.

DOI:10.1021/acs.analchem.4c03959
PMID:39308213
Abstract

CRISPR-Cas-based point-of-care testing (POCT) strategies have been widely explored for the detection of diverse biomarkers. However, these methods often require complicated operations, such as careful solution transfer steps, to achieve high sensitivity and accuracy. In this study, we combine a filter membrane-based POCT method with CRISPR-Cas12a for colorimetric detection of biomarkers. For the nucleic acid target, the trans-cleavage activity of CRISPR-Cas12a is directly triggered, cutting the single-stranded DNA linkers on glucose oxidase (GOx)-modified polymer nanoparticles. Due to the size difference between GOx and the polymer nanoparticles, GOx can be separated using a filter membrane. The filtrate containing GOx reacts with the substrate to generate a colorimetric signal. For the non-nucleic acid target, the non-nucleic acid signal is converted into a nucleic acid signal that activates CRISPR-Cas12a, resulting in a colorimetric signal. The entire operation is easy to perform, and the signal can be directly observed via the naked eye, which circumvents the use of costly instruments. The developed strategy holds great promise for accurate and accessible POCT detection of disease biomarkers in resource-limited settings.

摘要

基于 CRISPR-Cas 的即时检测 (POCT) 策略已被广泛用于检测多种生物标志物。然而,这些方法通常需要复杂的操作,例如仔细的溶液转移步骤,以实现高灵敏度和准确性。在本研究中,我们将基于膜的 POCT 方法与 CRISPR-Cas12a 相结合,用于生物标志物的比色检测。对于核酸靶标,CRISPR-Cas12a 的转切割活性被直接触发,切割葡萄糖氧化酶 (GOx) 修饰的聚合物纳米颗粒上的单链 DNA 连接物。由于 GOx 和聚合物纳米颗粒的大小差异,GOx 可以用滤膜分离。含有 GOx 的滤液与底物反应生成比色信号。对于非核酸靶标,非核酸信号被转化为激活 CRISPR-Cas12a 的核酸信号,产生比色信号。整个操作易于进行,并且可以通过肉眼直接观察到信号,从而避免了使用昂贵的仪器。该开发策略有望在资源有限的环境中实现疾病生物标志物的准确、便捷的 POCT 检测。

相似文献

1
Filter Membrane-Based Colorimetric Approach for Point-of-Care Detection of Biomarkers Using CRISPR-Cas12a.基于滤膜的比色法用于基于 CRISPR-Cas12a 的即时检测生物标志物
Anal Chem. 2024 Oct 1;96(39):15789-15796. doi: 10.1021/acs.analchem.4c03959. Epub 2024 Sep 23.
2
AND Logic-Gate-Based CRISPR/Cas12a Biosensing Platform for the Sensitive Colorimetric Detection of Dual miRNAs.基于 AND 逻辑门的 CRISPR/Cas12a 生物传感平台用于双重 miRNA 的灵敏比色检测。
Anal Chem. 2022 Nov 15;94(45):15839-15846. doi: 10.1021/acs.analchem.2c03666. Epub 2022 Nov 1.
3
Strand Displacement Amplification Assisted CRISPR-Cas12a Strategy for Colorimetric Analysis of Viral Nucleic Acid.基于链替代扩增辅助 CRISPR-Cas12a 策略的病毒核酸比色分析方法
Anal Chem. 2021 Nov 16;93(45):15216-15223. doi: 10.1021/acs.analchem.1c04133. Epub 2021 Nov 4.
4
CRISPR/Cas12a-Enabled Amplification-Free Colorimetric Visual Sensing Strategy for Point-of-Care Diagnostics of Biomarkers.用于生物标志物即时诊断的基于CRISPR/Cas12a的无扩增比色视觉传感策略
Anal Chem. 2025 Jan 14;97(1):1019-1027. doi: 10.1021/acs.analchem.4c06196. Epub 2024 Dec 19.
5
CRISPR-Cas12a-mediated dual-enzyme cascade amplification for sensitive colorimetric detection of HPV-16 target and ATP.CRISPR-Cas12a 介导的双酶级联扩增用于 HPV-16 靶标和 ATP 的灵敏比色检测。
Talanta. 2024 Jan 1;266(Pt 2):125050. doi: 10.1016/j.talanta.2023.125050. Epub 2023 Aug 7.
6
High-efficiency detection of APE1 using a defective PAM-driven CRISPR-Cas12a self-catalytic biosensor.使用有缺陷的PAM驱动的CRISPR-Cas12a自催化生物传感器高效检测APE1
Biosens Bioelectron. 2025 Jul 1;279:117410. doi: 10.1016/j.bios.2025.117410. Epub 2025 Mar 24.
7
The development of a fluorescence/colorimetric biosensor based on the cleavage activity of CRISPR-Cas12a for the detection of non-nucleic acid targets.基于 CRISPR-Cas12a 的核酸酶活性开发用于检测非核酸靶标的荧光/比色生物传感器。
J Hazard Mater. 2023 May 5;449:131044. doi: 10.1016/j.jhazmat.2023.131044. Epub 2023 Feb 20.
8
Visual and colorimetric detection of microRNA in clinical samples based on strand displacement amplification and nanozyme-mediated CRISPR-Cas12a system.基于链置换扩增和纳米酶介导的CRISPR-Cas12a系统对临床样本中的微小RNA进行可视化和比色检测。
Talanta. 2024 Sep 1;277:126310. doi: 10.1016/j.talanta.2024.126310. Epub 2024 May 21.
9
A CRISPR-Cas12a-mediated dual-mode luminescence and colorimetric nucleic acid biosensing platform based on upconversion nanozyme.一种基于上转换纳米酶的CRISPR-Cas12a介导的双模式发光和比色核酸生物传感平台。
Biosens Bioelectron. 2025 Feb 15;270:116963. doi: 10.1016/j.bios.2024.116963. Epub 2024 Nov 19.
10
Structure-switching G-quadruplex: An efficient CRISPR/Cas12a signal reporter for label-free colorimetric biosensing.结构转换型G-四链体:一种用于无标记比色生物传感的高效CRISPR/Cas12a信号报告分子。
Int J Biol Macromol. 2025 May;307(Pt 4):142410. doi: 10.1016/j.ijbiomac.2025.142410. Epub 2025 Mar 21.

引用本文的文献

1
Dual Detection of Glucose Using Commercial Potassium Permanganate and Glucose Oxidase: Colorimetric and Absorbance-Based Approaches.使用市售高锰酸钾和葡萄糖氧化酶对葡萄糖进行双检测:比色法和基于吸光度的方法。
ACS Omega. 2025 Aug 15;10(33):37514-37523. doi: 10.1021/acsomega.5c03564. eCollection 2025 Aug 26.