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Updated: May 21, 2025

Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay
Published on: May 3, 2018
Mimicking phosphatase function using Ce4+-modified metal-organic frameworks as heterogeneous catalysts for the
Hui Ran1, Yusha Huang2, Qi Wang1
1Chongqing Key Laboratory of Inorganic Functional Materials, College of Chemistry, Chongqing Normal University, Chongqing, 401331, China.
Abstract:
In this study, a general approach to prepare metal-organic framework (MOF)-based heterogeneous catalysts is proposed. The Ce4+-modified MOFs were obtained by the co-precipitation of catalytic active Ce4+ ions and catalytic inactive MOFs (ZIF-67, MOF-5, and ZIF-8). The Ce4+-modified MOFs retained the phosphatase-like activity of Ce4+ ions and were used for the fluorescent detection of phosphorylated amino acids by using o-phospho-L-tyrosine (p-Tyr) as a model target. Using Ce4+-modified ZIF-67 particles as the heterogeneous catalysts, the linear range for p-Tyr detection is 1-10 µM with a detection limit of 0.26 µM. Compared with homogeneous Ce4+ ion catalysts, a significant improvement in the sensitivity was achieved by using Ce4+-modified ZIF-67 particles as heterogeneous catalysts (from 11.21 to 0.26 µM). As the proposed method holds great promise in the fluorescent detection of phosphorylated amino acids, the Ce4+-modified ZIF-67-based catalytic system was further used for the discrimination of normal peptides and phosphorylated peptides with excellent resolution.
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