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基于二氧化钛修饰的单壁碳纳米角纳米复合材料定制的新型用于蛋白酪氨酸磷酸酶 1B 检测的荧光生物传感器。

Novel fluorescence biosensor custom-made for protein tyrosine phosphatase 1B detection based on titanium dioxide-decorated single-walled carbon nanohorn nanocomposite.

机构信息

College of Traditional Chinese Medicine and Food Engineering, Shanxi University of Chinese Medicine, Jinzhong 030619, China.

College of Traditional Chinese Medicine and Food Engineering, Shanxi University of Chinese Medicine, Jinzhong 030619, China.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2022 Nov 5;280:121548. doi: 10.1016/j.saa.2022.121548. Epub 2022 Jun 24.

DOI:10.1016/j.saa.2022.121548
PMID:35763945
Abstract

This paper presents a new fluorescent approach for the detection of protein tyrosine phosphatase 1B (PTP1B) based on titanium dioxide-decorated single-wall carbon nanohorns (TiO-SWCNHs). The novel TiO-SWCNHs nanocomposite was synthesized and characterized for the first time and the phosphorylated peptide as the substrate of PTP1B was designed. Properties of SWCNHs and TiO were combined by growing nano-sized TiO particles on SWCNHs, resulting in TiO-SWCNHs. TiO provides SWCNHs a large adsorption surface area and can specifically bind to phosphopeptide substrate. TiO-SWCNHs effectively quenched the fluorescence of the phosphorylated peptide substrate labeled by the fluorophore, and the system had a low fluorescence background. In the presence of PTP1B, dephosphorylation of the peptide occurred owing to the reaction between PTP1B and the peptide, causing the separation of the dye-labeled peptide from TiO-SWCNHs, which resulted in fluorescence enhancement of the reaction system. Thus, a simple and rapid strategy for the detection of PTP1B activity was developed, with a detection limit of 0.01 ng/mL and linear range of 0-10 ng/mL. The system can be used to detect PTP1B in serum using the standard addition method. This system provides a new approach for screening PTP1B inhibitors.

摘要

本文提出了一种基于二氧化钛修饰的单壁碳纳米角(TiO-SWCNHs)的新型荧光法检测蛋白酪氨酸磷酸酶 1B(PTP1B)。首次合成并表征了新型 TiO-SWCNHs 纳米复合材料,并设计了作为 PTP1B 底物的磷酸化肽。通过在 SWCNHs 上生长纳米级 TiO 颗粒,将 SWCNHs 和 TiO 的性质结合在一起,得到了 TiO-SWCNHs。TiO 为 SWCNHs 提供了较大的吸附表面积,并能特异性结合磷酸肽底物。TiO-SWCNHs 有效地猝灭了被荧光染料标记的磷酸化肽底物的荧光,且该体系具有较低的荧光背景。在 PTP1B 的存在下,由于 PTP1B 与肽的反应,导致肽从 TiO-SWCNHs 上脱磷酸化,从而使反应体系的荧光增强。因此,建立了一种简单快速检测 PTP1B 活性的方法,检测限为 0.01ng/mL,线性范围为 0-10ng/mL。该体系可采用标准添加法检测血清中的 PTP1B。该体系为筛选 PTP1B 抑制剂提供了一种新方法。

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