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Evaluation of enzyme kinetic characteristics of dipeptidyl peptidase 4 probe
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Ya-di ZHU1, 2, Jiang-hui LEI1, 3, Zi-yuan LI1, 3, Xing-kai QIAN1, *
Acta Pharmaceutica Sinica | 2026, 61(2) : 586 - 592
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Acta Pharmaceutica Sinica | 2026, 61(2): 586-592
• Original Articles •
Evaluation of enzyme kinetic characteristics of dipeptidyl peptidase 4 probe
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Ya-di ZHU1, 2, Jiang-hui LEI1, 3, Zi-yuan LI1, 3, Xing-kai QIAN1, *
Affiliations
  • 1Translational Medicine Research Center, Guizhou Medical University, Guiyang 561113, China
  • 2Guizhou Provincial Key Laboratory of Pathogenesis and Drug Research on Common Chronic Diseases, Guizhou Medical University, Guiyang 561113, China
  • 3School of Pharmaceutical Sciences, Guizhou Medical University, Guiyang 561113, China
Published: 2026-02-12 doi: 10.16438/j.0513-4870.2025-0401
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Dipeptidyl peptidase 4 (DPP4) is a serine protease widely present in human body, which can specifically catalyze the hydrolysis of proline (Pro) or alanine (Ala) peptide bond at the second N-terminal position of polypeptide chain. It is involved in the activation, partial or complete inactivation of a variety of bioactive polypeptides in vivo. In this study, the kinetic parameters of different probe substrates GP-PNA, GP-AMC and GP-BAN catalyzation by DPP4 were compared, and the inhibitory kinetic differences between DPP4 and its inhibitor sitagliptin/vildagliptin under different probe systems were studied. By means of molecular docking technology, the interaction mechanism between DPP4 and different substrates was revealed from the perspective of small molecules, and the key factors affecting the activity of DPP4 catalytic substrates were discussed. The results show that DPP4 has the best binding property to probe GP-BAN, and its affinity is higher than that of GP-AMC and GP-PNA, which proves that the carbon structure of probe is the key factor affecting the binding. Sitagliptin has better inhibitory activity on DPP4 than vildagliptin. The molecular docking results suggest that the halogenation characteristic of sitagliptin may be the key factor to enhance its binding ability. This study can provide an important basis for the selection of DPP4 probes under different research purposes, and also provide experimental data and research basis for rational design and development of highly selective DPP4 ligand tool molecules and personalized rational drug use in clinic.

dipeptidyl peptidase 4  /  probe  /  ligand  /  inhibitor  /  enzyme kinetics
朱雅迪, 雷江辉, 李梓媛, 钱星凯. 二肽基肽酶4探针酶动力学特征评价. 药学学报, 2026 , 61 (2) : 586 -592 . DOI: 10.16438/j.0513-4870.2025-0401
Ya-di ZHU, Jiang-hui LEI, Zi-yuan LI, Xing-kai QIAN. Evaluation of enzyme kinetic characteristics of dipeptidyl peptidase 4 probe[J]. Acta Pharmaceutica Sinica, 2026 , 61 (2) : 586 -592 . DOI: 10.16438/j.0513-4870.2025-0401
Year 2026 volume 61 Issue 2
217
106
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Article Info
doi: 10.16438/j.0513-4870.2025-0401
  • Receive Date:2025-04-10
  • Online Date:2026-09-21
  • Published:2026-02-12
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History
  • Received:2025-04-10
  • Revised:2025-06-05
Affiliations
    1Translational Medicine Research Center, Guizhou Medical University, Guiyang 561113, China
    2Guizhou Provincial Key Laboratory of Pathogenesis and Drug Research on Common Chronic Diseases, Guizhou Medical University, Guiyang 561113, China
    3School of Pharmaceutical Sciences, Guizhou Medical University, Guiyang 561113, China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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