Plasminogen activation by pro-urokinase in complex with its receptor - Dependence on a tripeptide (spectrozyme plasmin)

被引:15
作者
Wang, JY
Mazar, A
Quan, N
Schneider, A
Henkin, J
机构
[1] Abbott Laboratories, Abbott Park, IL
[2] D48 R. AP9-2124, Abbott Laboratories, Abbott Park, IL 60064-3500
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1997年 / 247卷 / 01期
关键词
urokinase; urokinase receptor; plasminogen; zymogen activation; extracellular proteolysis;
D O I
10.1111/j.1432-1033.1997.00256.x
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
The intrinsic activity of single-chain pro-urinary-type plasminogen activator (pro-uPA) and whether its receptor (uPAR) potentiates this activity remains controversial. In this report. the pro-uPAR/uPAR-(1-281)-peptide complex in solution is shown to have equivalent plasminogen-activator activity to that of active two-chain uPA (tc-uPA). However, the activity of the complex was dependent on a synthetic tripeptide, Spectrozyme plasmin (Sp1, H-D-2-aminohexanoic acid(Ahx)-hexatyrosyl-lysine-p-nitroanilide), which can also be used as a chromogenic substrate for plasmin. Furthermore, this activity could be completely suppressed by commonly used carrier proteins anti detergents. The pro-uPA/uPAR-(1-281)-peptide complex at 1 nM displayed similar activity to that of tc-uPA for either [Glu 1]plasminogen or [Lys77]plasminogen in chromogenic assays with Sp1 present as the plasmin substrate, When assayed with another plasmin substrate, S2251, the pro-uPA/uPAR-(1-281)-peptide complex was unable to activate plasminogen. The pro-uPA/uPAR-(1-281)-peptide complex and tc-uPA also showed a similar extent of plasminogen activation as measured by SDS/PAGE, when incubated with plasminogen and Spl in the presence of 100 mu M aprotinin, and plasminogen activation by pro-uPA alone was also stimulated in the presence of Spl in this assay. Activation of plasminogen by the pro-uPA/uPAR-(1-281)-peptide: strictly required the presence of Sp1, and pro-uPA remained in single-chain form during these assays. This activity of the pro-uPA/uPAR-(1-281)-peptide complex but not that of tc-uPA was completely inhibited by human serum albumin, bovine serum albumin, Tween-80, Triton X-100, and Pluronic-F68. Taken together, the data indicates that uPAR-(1-281)-peptide itself is not sufficient to augment pro-uPA activity and the presence of an effector molecule (e.g. Sp1) is required to elicit the full plasminogen-activator activity of the pro-uPA/uPAR-(1-781)-peptide complex. It remains to be seen whether there is a physiological counterpart to this phenomenon.
引用
收藏
页码:256 / 261
页数:6
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