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使用基于手性反转L-DNA的逻辑器件增强复杂环境中细胞识别的灵敏度。

Enhanced Sensitivity of Cell Identification in Complex Environments Using Chirally Inverted L-DNA-Based Logic Devices.

作者信息

Lai Zixi, Jin Di, Tian Yuan, Chen Xiaoxing, Han Da, Chen Haige, Wang Junyan, Yang Yang

机构信息

Shanghai Pulmonary Hospital, School of Medicine, Tongji University, Shanghai, 200092, China.

Institute of Molecular Medicine (IMM) and Department of Urology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, China.

出版信息

Adv Sci (Weinh). 2024 Dec;11(45):e2410642. doi: 10.1002/advs.202410642. Epub 2024 Oct 14.

DOI:10.1002/advs.202410642
PMID:39401418
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11615743/
Abstract

Accurate identification and isolation of target cells are crucial for precision diagnosis and treatment. DNA aptamer-based logic devices provide a distinct advantage in this context, as they can logically analyze multiple cell surface markers with high efficiency. However, the susceptibility of natural DNA (D-DNA) to degradation can compromise the sensitivity and specificity of these devices, potentially leading to false-positive and false-negative results, particularly in complex biological environments. To address this issue, dual- and triple-aptamer-based cell-surface logic devices are designed and developed using mirror-image L-DNA, a chiral molecule of D-DNA with high biostability. These devices allow for simultaneous analysis of multiple cell surface proteins, achieving greater specificity in cell identification and isolation than D-DNA-based logic devices. The L-DNA probes realized 98.7% and 70.5% sensitivities in FBS buffer with dual- and triple-aptamer-based logic devices for target cell identification, while D-DNA probes only showed 27.9% and 0.1%. It is believed that the high stability of L-DNA and the high efficiency of the devices for labeling cell subpopulations will have broad applications in the life sciences, biomedical engineering, and personalized medicine.

摘要

准确识别和分离靶细胞对于精确诊断和治疗至关重要。基于DNA适配体的逻辑器件在这方面具有显著优势,因为它们能够高效地对多种细胞表面标志物进行逻辑分析。然而,天然DNA(D-DNA)易降解的特性可能会影响这些器件的灵敏度和特异性,从而可能导致假阳性和假阴性结果,尤其是在复杂的生物环境中。为了解决这个问题,人们利用镜像L-DNA(D-DNA的一种具有高生物稳定性的手性分子)设计并开发了基于双适配体和三适配体的细胞表面逻辑器件。这些器件能够同时分析多种细胞表面蛋白,在细胞识别和分离方面比基于D-DNA的逻辑器件具有更高的特异性。在含胎牛血清的缓冲液中,用于靶细胞识别的基于双适配体和三适配体的逻辑器件中的L-DNA探针实现了98.7%和70.5%的灵敏度,而D-DNA探针仅显示出27.9%和0.1%的灵敏度。人们认为,L-DNA的高稳定性以及这些器件标记细胞亚群的高效率将在生命科学、生物医学工程和个性化医疗中具有广泛的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6f4/11615743/43c6c3f92d7e/ADVS-11-2410642-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6f4/11615743/4cf996035d3b/ADVS-11-2410642-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6f4/11615743/aa850efe4972/ADVS-11-2410642-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6f4/11615743/054a08863dc6/ADVS-11-2410642-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6f4/11615743/43c6c3f92d7e/ADVS-11-2410642-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6f4/11615743/4cf996035d3b/ADVS-11-2410642-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6f4/11615743/aa850efe4972/ADVS-11-2410642-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6f4/11615743/054a08863dc6/ADVS-11-2410642-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6f4/11615743/43c6c3f92d7e/ADVS-11-2410642-g001.jpg

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本文引用的文献

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FINDER: A Fluidly Confined CRISPR-Based DNA Reporter on Living Cell Membranes for Rapid and Sensitive Cancer Cell Identification.FINDER:一种在活细胞膜上的基于 CRISPR 的流体限制型 DNA 报告基因,用于快速灵敏的癌细胞鉴定。
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