ARE DIPROTIN-A (ILE-PRO-ILE) AND DIPROTIN-B (VAL-PRO-LEU) INHIBITORS OR SUBSTRATES OF DIPEPTIDYL PEPTIDASE-IV

被引:124
作者
RAHFELD, J
SCHIERHORN, M
HARTRODT, B
NEUBERT, K
HEINS, J
机构
[1] MARTIN LUTHER UNIV,BIOTECHNIKUM HALLE,WEINBERGWEG 16A,O-4010 HALLE,GERMANY
[2] MARTIN LUTHER UNIV,DEPT CHEM,O-4010 HALLE,GERMANY
关键词
DIPEPTIDYL PEPTIDASE-IV; SUBSTRATE SPECIFICITY INHIBITION;
D O I
10.1016/0167-4838(91)90284-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dipeptidyl peptidase IV preferably hydrolyzes peptides and proteins with a penultimate proline residue. Umezawa and co-workers (Umezawa et al. (1984) J. Antibiotics 37, 422-425) reported that diprotin A (Ile-Pro-Ile) and diprotin B (Val-Pro-Leu) are inhibitors for dipeptidyl peptidase IV. We could show that both compounds as well as other tripeptides with a penultimate proline residue are substrates for dipeptidyl peptidase IV. An apparent competitive inhibition by those compounds is a kinetic artifact due to the substrate-like structure of such tripeptides.
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页码:314 / 316
页数:3
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