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双信号放大策略用于可视化癌症生物标志物蛋白的双分析物荧光适体传感器。

Double Signal Amplification Strategy for Dual-Analyte Fluorescent Aptasensors for Visualizing Cancer Biomarker Proteins.

机构信息

School of Resources and Environment, Hunan University of Technology and Business, Changsha, 410205 Hunan, P. R. China.

Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, Institute of Pharmacy & Pharmacology, Hengyang Medical School, University of South China, Hengyang, Hunan 421001, P. R. China.

出版信息

Anal Chem. 2022 Jul 26;94(29):10451-10461. doi: 10.1021/acs.analchem.2c01649. Epub 2022 Jul 13.

Abstract

The simultaneous analysis of diversified biomarkers with high sensitivity and in a point-of-care (POC) manner is of great significance for facile and early cancer diagnosis. Herein, we develop a target amplification-assisted ratiometric fluorescence assay (TARFA) platform integrating the dual-amplification strategy and colorimetric readout technology for sensitive and specific detection of two malignancy-associated biomarkers. Meanwhile, the NIR-excited alkaline-earth sulfide nanodots (ASNDs) with an ultrasmall (<10 nm) diameter and tunable emission wavelength are employed to replace commonly UV/visible light-excited fluorescent labels to minimize background interference from the sample matrix. Unique advantages of the ASNDs, together with superiority of consecutive signal amplification of enzymatic target recycling (ETR) and hybridization chain reaction (HCR), realize the pg/mL-range detection limit in specifically recognizing the vascular endothelial growth factor (VEGF) and soluble interleukin-6 receptors (sIL-6R). The combination detection of the dual analyte exhibits an improved sensitivity for cancer diagnosis. The addition of the target biomarkers leads to an increasingly ratiometric RGB signal, and quantification based on the ratio-dependent signal is more reliable rather than measuring the absolute RGB signals. Moreover, perceptible color transformation makes the TARFA platform competent for visual analysis of the target analytes as convenient as reading the pH indicator strip, and hue-based image analysis also improves the method with fine precision by quantitatively identifying the visual color. This work provides a new kind of NIR-excited aptasensing platform with a low detection limit, high throughput, and great portability, which also highlights the potential of the ASNDs in biomolecular fluorescent labeling.

摘要

同时分析具有高灵敏度和即时检测(POC)特点的多种生物标志物对于简便、早期癌症诊断具有重要意义。在此,我们开发了一种基于靶标扩增辅助比率荧光分析(TARFA)平台,整合了双重扩增策略和比色读取技术,用于灵敏和特异性检测两种与恶性肿瘤相关的生物标志物。同时,采用具有超小(<10nm)直径和可调发射波长的近红外激发的碱土硫化物纳米点(ASNDs)代替通常的紫外/可见光激发荧光标记物,以最小化来自样品基质的背景干扰。ASNDs 的独特优势,加上酶靶循环(ETR)和杂交链式反应(HCR)的连续信号放大的优势,实现了在特异性识别血管内皮生长因子(VEGF)和可溶性白细胞介素-6 受体(sIL-6R)时达到 pg/mL 级别的检测限。双分析物的组合检测提高了癌症诊断的灵敏度。加入靶标生物标志物会导致越来越多的比率比色信号,并且基于比率相关信号的定量比测量绝对 RGB 信号更可靠。此外,可感知的颜色转变使 TARFA 平台能够像读取 pH 指示剂条一样方便地进行目标分析物的可视化分析,并且基于色调的图像分析通过定量识别视觉颜色也提高了方法的精度。这项工作提供了一种具有低检测限、高通量和便携性的新型近红外激发适体传感平台,同时也突出了 ASNDs 在生物分子荧光标记中的潜力。

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