Amino-terminal truncation of procalcitonin, a marker for systemic bacterial infections, by dipeptidyl peptidase IV (DP IV)

被引:81
作者
Wrenger, S
Kähne, T
Bohuon, C
Weglöhner, W
Ansorge, S
Reinhold, D
机构
[1] Univ Magdeburg, Inst Expt Internal Med, D-39120 Magdeburg, Germany
[2] Inst Gustave Roussy, Dept Biol Clin, F-94805 Villejuif, France
[3] INVIVO Diagnost Entwicklungsgesell MnH, D-16761 Hennigsdorf, Germany
关键词
procalcitonin; dipeptidyl peptidase IV;
D O I
10.1016/S0014-5793(99)01779-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Increased concentrations of procalcitonin (PCT) are found in the plasma of patients with thermal injury and in patients with sepsis and severe infection, making this molecule important as a diagnostic and prognostic marker in these diseases. Interestingly, only the truncated form of PCT, PCT(3-116), is present in the plasma of these patients. The enzyme responsible for this truncation is unknown as yet. Here, using capillary zone electrophoresis, mass spectrometry and Edman sequence analysis, we demonstrate that dipeptidyl peptidase IV (DP IV, EC 3.4.14.5) is capable of catalyzing the hydrolysis of PCT(1-116), releasing the N-terminal dipeptide Ale-Pro. We hypothesize that PCT(3-116) is the result of the hydrolysis of PCT(1-116) by soluble DP IV of the blood plasma or by DP IV expressed on the surface of cells. (C) 2000 Federation of European Biochemical Societies.
引用
收藏
页码:155 / 159
页数:5
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