Suggested functions for prolyl oligopeptidase:: A puzzling paradox

被引:75
作者
Brandt, Inger [1 ]
Scharpe, Simon [1 ]
Lambeir, Anne-Marie [1 ]
机构
[1] Univ Antwerp VIB, Dept Pharmaceut Sci, Med Biochem Lab, B-2610 Antwerp, Wilrijk, Belgium
关键词
prolyl oligopeptidase; serine protease; inositolphosphate; brain; neuropeptide;
D O I
10.1016/j.cca.2006.09.001
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Prolyl oligopeptidase (PO, E.C. 3.4.21.26) is a post-proline cleaving enzyme with endopeptidase activity towards peptides not longer than 30 amino acids. It has been purified and characterized from various mammalian and bacterial sources, but despite its thorough enzymological and structural characterization, the exact function of PO remains obscure. Many investigations have addressed the physiological role of this enzyme, mainly by the use of specific PO inhibitors, activity measurements in clinical samples and (neuro)peptide degradation studies. From the combined results emerges a puzzling paradox: how can an intracellular, cytoplasmatic oligopeptidase affect not only the amount of extracellular neuropeptides but also signal transduction and secretion? This report provides a review of the literature on the suggested functions for PO, highlighting possible pitfalls and contradictions. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:50 / 61
页数:12
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