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一种基于温和还原激活的 CRISPR/Cas12a 系统的电化学生物传感器,用于灵敏检测循环肿瘤细胞。

An electrochemical biosensor based on mild reduction-activated CRISPR/Cas12a system for sensitive detection of circulating tumor cells.

机构信息

State Key Laboratory of Analytical Chemistry for Life Science, School of Life Sciences, Nanjing University, Nanjing, 210023, PR China.

State Key Laboratory of Analytical Chemistry for Life Science, School of Life Sciences, Nanjing University, Nanjing, 210023, PR China; Center for Molecular Recognition and Biosensing, Shanghai Engineering Research Center of Organ Repair, School of Life Sciences, Shanghai University, Shanghai, 200444, PR China.

出版信息

Biosens Bioelectron. 2024 Oct 15;262:116550. doi: 10.1016/j.bios.2024.116550. Epub 2024 Jul 6.

DOI:10.1016/j.bios.2024.116550
PMID:38976958
Abstract

Circulating tumor cell (CTC) has been a valuable biomarker for the diagnosis of breast cancer, while folate receptor is a kind of cell surface receptor glycoprotein which is overexpressed in breast cancer. In this work, we have designed and fabricated an electrochemical biosensor for sensitive detection of folate receptor-positive CTCs based on mild reduction assisted CRISPR/Cas system. Specifically, folate functionalized magnetic beads are firstly prepared to capture CTCs owing to the strong affinity between folate and the folate receptors on the surface of cells. Then, the cell membranes are treated by mild reduction so as to expose a large number of free sulfhydryl groups, which can be coupled with maleimide-DNA to introduce the signal amplified CRISPR/Cas12a system. After the trans-cleavage activity of CRISPR/Cas12a is activated, the long chain DNA modified with electroactive molecules methylene blue can be randomly cleaved into short DNA fragments, which are then captured on the graphite electrode through the host-guest recognition with cucurbit [7]uril, generating highly amplified electrochemical signal corresponding to the number of CTCs. The electrochemical biosensor not only demonstrates the sensitivity with a low detection limit of 2 cells/mL, but also highlights its excellent selectivity and stability in complex environment. Therefore, our biosensor may provide an alternative tool for the analysis of CTCs.

摘要

循环肿瘤细胞 (CTC) 一直是乳腺癌诊断的有价值的生物标志物,而叶酸受体是一种细胞表面受体糖蛋白,在乳腺癌中过度表达。在这项工作中,我们设计并制造了一种基于温和还原辅助 CRISPR/Cas 系统的用于灵敏检测叶酸受体阳性 CTC 的电化学生物传感器。具体来说,叶酸功能化的磁性珠首先被制备以捕获 CTC,因为叶酸与细胞表面上的叶酸受体之间存在很强的亲和力。然后,通过温和还原处理细胞膜,以暴露出大量游离的巯基,这些巯基可以与马来酰亚胺-DNA 偶联,引入信号放大的 CRISPR/Cas12a 系统。在 CRISPR/Cas12a 的转切割活性被激活后,带有电化学活性分子亚甲基蓝的长链 DNA 可以随机切割成短的 DNA 片段,然后通过与瓜环 [7] 脲的主客体识别被捕获在石墨电极上,产生与 CTC 数量相对应的高度放大的电化学信号。电化学生物传感器不仅具有低至 2 个细胞/mL 的检测限的灵敏度,而且在复杂环境中表现出优异的选择性和稳定性。因此,我们的生物传感器可为 CTC 的分析提供一种替代工具。

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