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A Signal-On Fluorosensor Based on Quench-Release Principle for Sensitive Detection of Antibiotic Rapamycin

机译:基于淬灭释放原理的信号荧光传感器对雷帕霉素的灵敏检测

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摘要

An antibiotic rapamycin is one of the most commonly used immunosuppressive drugs, and also implicated for its anti-cancer activity. Hence, the determination of its blood level after organ transplantation or tumor treatment is of great concern in medicine. Although there are several rapamycin detection methods, many of them have limited sensitivity, and/or need complicated procedures and long assay time. As a novel fluorescent biosensor for rapamycin, here we propose “Q’-body”, which works on the fluorescence quench-release principle inspired by the antibody-based quenchbody (Q-body) technology. We constructed rapamycin Q’-bodies by linking the two interacting domains FKBP12 and FRB, whose association is triggered by rapamycin. The fusion proteins were each incorporated position-specifically with one of fluorescence dyes ATTO520, tetramethylrhodamine, or ATTO590 using a cell-free translation system. As a result, rapid rapamycin dose-dependent fluorescence increase derived of Q’-bodies was observed, especially for those with ATTO520 with a lowest detection limit of 0.65 nM, which indicates its utility as a novel fluorescent biosensor for rapamycin.
机译:雷帕霉素抗生素是最常用的免疫抑制药物之一,还涉及其抗癌活性。因此,在器官移植或肿瘤治疗后确定其血液水平是医学上非常关注的问题。尽管有几种雷帕霉素检测方法,但是它们中的许多方法灵敏度有限,并且/或者需要复杂的程序和较长的测定时间。作为雷帕霉素的新型荧光生物传感器,我们在此提出“ Q’-body”,其基于基于抗体的猝灭抗体(Q-body)技术启发的荧光猝灭释放原理。我们将雷帕霉素触发的两个相互作用域FKBP12和FRB连接在一起,从而构建了雷帕霉素Q'体。使用无细胞翻译系统,将融合蛋白各自与荧光染料ATTO520,四甲基罗丹明或ATTO590之一位置特异性地结合。结果,观察到了雷帕霉素从Q’-体衍生的剂量依赖性荧光的快速增加,特别是对于那些最低检出限为0.65 nM的ATTO520的雷帕霉素,这表明其可用作雷帕霉素的新型荧光生物传感器。

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