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通过催化非活性金属离子加速 Uio-66-NH 的磷酸酶样活性及其在心肌肌钙蛋白 I 荧光检测中应用的研究

Accelerating the Phosphatase-like Activity of Uio-66-NH by Catalytically Inactive Metal Ions and Its Application for Improved Fluorescence Detection of Cardiac Troponin I.

机构信息

Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, Innovative Drug Research Center, School of Pharmaceutical Sciences, Chongqing University, Chongqing 401331, China.

School of Chemistry and Chemical Engineering, Chongqing Key Laboratory of Theoretical and Computational Chemistry, Chongqing University, Chongqing 401331, China.

出版信息

Anal Chem. 2024 Feb 13;96(6):2684-2691. doi: 10.1021/acs.analchem.3c05499. Epub 2024 Feb 2.

Abstract

Compared with natural enzymes, nanozymes usually exhibit much lower catalytic activities, which limit the sensitivities of nanozyme-based immunoassays. Herein, several metal ions without enzyme-like activities were engineered onto Uio-66-NH nanozyme through postsynthetic modification. The obtained M@Uio-66-NH (M = Zn, Cd, Co, Caand Ni) exhibited improved phosphatase-like catalytic activities. In particular, a 12-fold increase in the catalytic efficiency (/) of Uio-66-NH was observed after the modification with Zn. Mechanism investigations indicate that both the amino groups and oxygen-containing functional groups in Uio-66-NH are the binding sites of Zn, and the modified Zn ions on Uio-66-NH serve as the additional catalytic sites for improving the catalytic performance. Furthermore, the highly active Zn@Uio-66-NH was used as a nanozyme label to develop a fluorescence immunoassay method for the detection of cardiac troponin I (cTnI). Compared with pristine Uio-66-NH, Zn@Uio-66-NH can widen the linear range by 1 order of magnitude (from 10 pg/mL-1 μg/mL to 1 pg/mL-1 μg/mL) and also lower the detection limit by 5 times (from 4.7 pg/mL to 0.9 pg/mL).

摘要

与天然酶相比,纳米酶通常表现出低得多的催化活性,这限制了基于纳米酶的免疫分析的灵敏度。在此,通过后合成修饰将几种没有酶样活性的金属离子工程化到 Uio-66-NH 纳米酶上。所得的 M@Uio-66-NH(M = Zn、Cd、Co、Ca 和 Ni)表现出增强的磷酸酶样催化活性。特别是,在用 Zn 修饰后,Uio-66-NH 的催化效率(/)提高了 12 倍。机理研究表明,Uio-66-NH 中的氨基和含氧官能团都是 Zn 的结合位点,修饰在 Uio-66-NH 上的改性 Zn 离子作为额外的催化位点,以提高催化性能。此外,高活性的 Zn@Uio-66-NH 被用作纳米酶标记物,开发了用于检测心肌肌钙蛋白 I(cTnI)的荧光免疫分析方法。与原始的 Uio-66-NH 相比,Zn@Uio-66-NH 可以将线性范围扩大 1 个数量级(从 10 pg/mL-1 μg/mL 到 1 pg/mL-1 μg/mL),并将检测限降低 5 倍(从 4.7 pg/mL 到 0.9 pg/mL)。

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