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Integrating Highly Efficient Recognition and Signal Transition of g-C3N4 Embellished Ti3C2 MXene Hybrid Nanosheets for Electrogenerated Chemiluminescence Analysis of Protein Kinase Activity

机译:基于蛋白激酶活性的高效识别和信号过渡G-C3N4缀饰Ti3C2 mxOne型纳米液相色谱分析

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摘要

Herein, a novel electrogenerated chemiluminescence (ECL) method for highly sensitive kinase activity and inhibitors screening was developed based on graphitic carbon nitride nanosheet (g-C3N4) nanoparticle embellished titanium carbide (Ti3C2) MXene nanosheets, integrating the highly efficient recognition and signal amplification activity. In this strategy, kemptide was first immobilized onto a gold electrode, and it was phosphorylated by the protein kinase A which was used as a model. The g-C3N4-MXene probe can adsorb explicitly onto the electrode based on chelation between the phosphate group and Ti defect sites enriched in MXenes. Besides the abundant active sites on MXene for the highly efficient binding with phosphate groups, the Ti3C2 MXene not only provides a unique conductive platform to accommodate more g-C3N4 nanoparticles but also facilitates the electron transfer on the electrode interface and suppresses the passivation of g-C3N4 that explores their highly efficient ECL emission with high stability. The obtained ECL signals were closely related to the kinase activity and can be applied for protein kinase A (PKA) activity detection. Under the optimal conditions, the proposed ECL biosensor provided a quantitative readout to PKA concentration in the range 0.015-40 U mL(-1) with the detection limit of 1.0 mU mL(-1). The ECL biosensor was also successfully applied to monitor drug-triggered kinase activation and quantitative analysis of the kinase inhibitors in MCF-7 cell lysates. This work shows that the proposed ECL biosensor has the potential to be a powerful tool for PKA study and clinical diagnostics as well as the discovery of new targeted drugs.
机译:在此,基于石墨碳氮化物纳米片(G-C3N4)纳米颗粒缀饰钛碳化物(Ti3C2)MXENE纳米晶片(Ti3C2)乳腺纳米液(Ti3C2)纳米粒子的抑制剂筛选的一种新型电化学化学发光(ECL)方法。集成了高效识别和信号放大活性。在该策略中,首先将刺酮固定在金电极上,并且通过用作模型的蛋白激酶A磷酸化。 G-C3N4-偏烯探针可以基于富含MxENES富集的磷酸盐基团和Ti缺陷位点之间的螯合来明确地吸附到电极上。除了与磷酸基团高效结合的MXEN上的丰富活性位点之外,Ti3c2 mxene不仅提供了独特的导电平台,以适应更多G-C3N4纳米颗粒,还可以促进电极接口上的电子转移并抑制G-的钝化C3N4探讨了具有高稳定性的高效ECL排放。所获得的ECL信号与激酶活性密切相关,可用于蛋白激酶A(PKA)活性检测。在最佳条件下,所提出的ECOR生物传感器在0.015-40uml(-1)范围内提供定量读出在0.015-40uml(-1)的范围内,检测限为1.0μm1(-1)。 ECL生物传感器还成功地应用于监测MCF-7细胞裂解物中激酶抑制剂的药物触发激酶活化和定量分析。这项工作表明,拟议的ECL生物传感器有可能成为PKA学习和临床诊断的强大工具,以及对新的目标药物的发现。

著录项

  • 来源
    《Analytical chemistry》 |2020年第15期|共9页
  • 作者单位

    Hunan Normal Univ Coll Chem &

    Chem Engn Key Lab Chem Biol &

    Tradit Chinese Med Res Minist Educ Changsha 410081 Peoples R China;

    Tsinghua Univ Dept Chem Beijing Key Lab Analyt Methods &

    Instrumentat Key Lab Bioorgan Phosphorus Chem &

    Chem Biol Mini Beijing 100084 Peoples R China;

    Tsinghua Univ Dept Chem Beijing Key Lab Analyt Methods &

    Instrumentat Key Lab Bioorgan Phosphorus Chem &

    Chem Biol Mini Beijing 100084 Peoples R China;

    Hunan Normal Univ Coll Chem &

    Chem Engn Key Lab Chem Biol &

    Tradit Chinese Med Res Minist Educ Changsha 410081 Peoples R China;

    Tsinghua Univ Dept Chem Beijing Key Lab Analyt Methods &

    Instrumentat Key Lab Bioorgan Phosphorus Chem &

    Chem Biol Mini Beijing 100084 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
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