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基于氧化石墨烯荧光开关的多功能 G-四链体发夹探针的无标记和无酶转录因子检测。

Label-free and enzyme-free detection of transcription factors with graphene oxide fluorescence switch-based multifunctional G-quadruplex-hairpin probe.

机构信息

Key Laboratory for Colloid and Interface Chemistry of Education Ministry, School of Chemistry and Chemical Engineering, Shandong University, 250100 Jinan, PR China.

School of Pharmaceutical Sciences, Shandong University, 250012 Jinan, PR China.

出版信息

Biosens Bioelectron. 2016 Jan 15;75:155-60. doi: 10.1016/j.bios.2015.08.034. Epub 2015 Aug 19.

DOI:10.1016/j.bios.2015.08.034
PMID:26318784
Abstract

Transcription factors (TFs) play pivotal roles in the regulation of a variety of essential cellular processes and some of them have been recognized as potential diagnostic markers and therapeutic targets of some diseases. Sensitive and accurate detection of TFs is of great importance to better understanding their roles in gene regulation and evaluation of disease state. Here, we developed a simple, label-free and enzyme-free new fluorescent strategy for the detection of TFs by graphene oxide (GO) fluorescence switch-based multifunctional G-quadruplex-hairpin probe (MGHP). The MGHP possessed of three functions simultaneously, adsorbing onto GO with the loop part, binding to target with the stem part and serving as signal carrier with the terminal G-quadruplex. First, the MGHP was adsorbed quickly to GO. Next, the TF bound to the stem part of MGHP to form a huge target-MGHP complex, which led to desorption of the complex from GO. Finally, NMM was inserted into G-quadruplex in the complex to yield an enhanced fluorescence response. The GO used here, as a fluorescence switch, could quickly and efficiently quench the fluorescence of NMM inserted into the MGHP absorbed on the GO, guaranteeing a high signal-to-noise ratio. Sensitive detection of purified NF-κB p50 and HeLa cell nuclear extracts were achieved with detection limits of 0.2nM and 7.8ng/µL, respectively. Moreover, this proposed strategy could be used to screen inhibitors of NF-κB p50 activity. The strategy proposed here might offer a new potential approach for reliable quantification of TFs in clinical diagnostics and treatment research of some diseases.

摘要

转录因子 (TFs) 在调节多种重要细胞过程中发挥着关键作用,其中一些已被认为是某些疾病的潜在诊断标志物和治疗靶点。TFs 的灵敏和准确检测对于更好地理解它们在基因调控中的作用以及评估疾病状态非常重要。在这里,我们开发了一种简单、无标记和无酶的新荧光策略,基于石墨烯氧化物 (GO) 荧光开关的多功能 G-四链体发夹探针 (MGHP) 用于检测 TFs。MGHP 同时具有三种功能,通过环部分吸附在 GO 上,通过茎部分与靶标结合,并作为带有末端 G-四链体的信号载体。首先,MGHP 快速吸附到 GO 上。接下来,TF 与 MGHP 的茎部结合形成巨大的靶标-MGHP 复合物,导致复合物从 GO 上解吸。最后,NMM 插入到复合物中的 G-四链体中,产生增强的荧光响应。这里使用的 GO 作为荧光开关,可以快速有效地猝灭插入到吸附在 GO 上的 MGHP 中的 NMM 的荧光,保证了高的信噪比。通过该方法可实现对纯化 NF-κB p50 和 HeLa 细胞核提取物的灵敏检测,检测限分别为 0.2nM 和 7.8ng/µL。此外,该策略还可用于筛选 NF-κB p50 活性抑制剂。本研究提出的策略为临床诊断中 TFs 的可靠定量以及某些疾病的治疗研究提供了一种新的潜在方法。

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