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基于酶激活自主运动 DNA zyme 信号放大策略的肿瘤细胞特异性分子成像技术,提高了空间特异性。

Enzymatically Activated Autonomous-Motion DNAzyme Signal Amplification Strategy for Tumor Cell-Specific Molecular Imaging with Improved Spatial Specificity.

机构信息

Key Laboratory of Optic-Electric Sensing and Analytical Chemistry for Life Science, MOE, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, P. R. China.

School of Municipal and Environmental Engineering, Shandong Jianzhu University, Jinan 250101, Shandong, P. R. China.

出版信息

Anal Chem. 2023 Jun 20;95(24):9388-9395. doi: 10.1021/acs.analchem.3c01963. Epub 2023 Jun 6.

Abstract

Strategies for achieving tumor-specific molecular imaging based on signal amplification hold great potential for evaluating the risk of tumor metastasis and progression. However, traditional amplification strategies are still constrained with limited tumor specificity because of the off-tumor signal leakage. Herein, an endogenous enzyme-activated autonomous-motion DNAzyme signal amplification strategy (E-DNAzyme) was rationally designed for tumor-specific molecular imaging with improved spatial specificity. The sensing function of E-DNAzyme can be specifically activated by the overexpressed apurinic/apyrimidinic endonuclease 1 (APE1) in the cytoplasm of tumor cells instead of normal cells, ensuring the tumor cell-specific molecular imaging with improved spatial specificity. Of note, benefiting from the target analogue-triggered autonomous motion of the DNAzyme signal amplification strategy, the detection limit can be decreased by approx. ∼7.8 times. Moreover, the discrimination ratio of tumor/normal cells of the proposed E-DNAzyme was ∼3.44-fold higher than the traditional amplification strategy, indicating the prospect of this universal design for tumor-specific molecular imaging.

摘要

基于信号放大的肿瘤特异性分子成像策略在评估肿瘤转移和进展风险方面具有很大的潜力。然而,由于肿瘤外信号泄漏,传统的放大策略仍然受到肿瘤特异性的限制。在此,设计了一种内源性酶激活自主运动 DNAzyme 信号放大策略 (E-DNAzyme),用于具有改善空间特异性的肿瘤特异性分子成像。E-DNAzyme 的传感功能可以被肿瘤细胞质中过表达的脱嘌呤/脱嘧啶内切酶 1 (APE1) 特异性激活,而不是正常细胞,从而保证了具有改善空间特异性的肿瘤细胞特异性分子成像。值得注意的是,受益于目标类似物触发的 DNAzyme 信号放大策略的自主运动,检测限可降低约 7.8 倍。此外,所提出的 E-DNAzyme 的肿瘤/正常细胞的区分率比传统的放大策略高约 3.44 倍,表明这种通用设计用于肿瘤特异性分子成像的前景。

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