Levashov M Yu, Aisina R B, Gershkovich K B, Varfolomeyev S D
Chemical Faculty, Lomonosov Moscow State University, Moscow, 119992, Russia.
Biochemistry (Mosc). 2007 Jul;72(7):707-15. doi: 10.1134/s0006297907070048.
Stimulation of Lys-plasminogen (Lys-Pg) and Glu-plasminogen (Glu-Pg) activation under the action of staphylokinase and Glu-Pg activation under the action of preformed plasmin-staphylokinase activator complex (Pm-STA) by low concentrations and inhibition by high concentrations of omega-amino acids (>90-140 mM) were found. Maximal stimulation of the activation was observed at concentrations of L-lysine, 6-aminohexanoic acid (6-AHA), and trans-(4-aminomethyl)cyclohexanecarboxylic acid 8.0, 2.0, and 0.8 mM, respectively. In contrast, the Lys-Pg activation rate by Pm-STA complex sharply decreased when concentrations of omega-amino acids exceeded the above-mentioned values. It was found that formation of Pm-STA complex from a mixture of equimolar concentrations of staphylokinase and Glu-Pg or Lys-Pg is stimulated by low concentrations (maximal at 10 mM) of 6-AHA. Negligible increase in the specific activities of plasmin and Pm-STA complex was detected at higher concentrations of 6-AHA (to maximal at 70 and 50 mM, respectively). Inhibitory effects of omega-amino acids on the rate of fibrinolysis induced by staphylokinase, Pm-STA complex, and plasmin were compared. It was found that inhibition of staphylokinase-induced fibrinolysis by omega-amino acids includes blocking of the reactions of Pm-STA complex formation, plasminogen activation by this complex, and lysis of fibrin by forming plasmin as a result of displacement of plasminogen and plasmin from the fibrin surface. Thus, the slow stage of Pm-STA complex formation plays an important role in the mechanism of action of omega-amino acids on Glu-Pg activation and fibrinolysis induced by staphylokinase. In addition to alpha-->beta change of Glu-Pg conformation, stimulation of Pm-STA complex formation leads to increase in Glu-Pg activation rate in the presence of low concentrations of omega-amino acids. Inhibition of Pm-STA complex formation on fibrin surface by omega-amino acids is responsible for appearance of long lag phases on curves of fibrinolysis induced by staphylokinase.
发现在低浓度下,葡萄球菌激酶可刺激赖氨酸纤溶酶原(Lys-Pg)和谷氨酸纤溶酶原(Glu-Pg)的激活,预先形成的纤溶酶 - 葡萄球菌激酶激活复合物(Pm-STA)可刺激Glu-Pg的激活;而高浓度(>90 - 140 mM)的ω-氨基酸则具有抑制作用。在L-赖氨酸、6-氨基己酸(-AHA)和反式-(4-氨甲基)环己烷羧酸的浓度分别为8.0、2.0和0.8 mM时,观察到激活的最大刺激作用。相反,当ω-氨基酸浓度超过上述值时,Pm-STA复合物对Lys-Pg的激活率急剧下降。研究发现,等摩尔浓度的葡萄球菌激酶与Glu-Pg或Lys-Pg混合形成Pm-STA复合物时,低浓度(10 mM时最大)的6-AHA具有刺激作用。在较高浓度的6-AHA(分别在70和50 mM时最大)下,纤溶酶和Pm-STA复合物的比活性仅有可忽略不计的增加。比较了ω-氨基酸对葡萄球菌激酶、Pm-STA复合物和纤溶酶诱导的纤维蛋白溶解速率的抑制作用。发现ω-氨基酸对葡萄球菌激酶诱导的纤维蛋白溶解的抑制作用包括阻断Pm-STA复合物的形成反应、该复合物对纤溶酶原的激活以及由于纤溶酶原和纤溶酶从纤维蛋白表面被置换而形成纤溶酶导致的纤维蛋白溶解。因此,Pm-STA复合物形成的缓慢阶段在ω-氨基酸对Glu-Pg激活和葡萄球菌激酶诱导的纤维蛋白溶解的作用机制中起重要作用。除了Glu-Pg构象的α→β变化外,在低浓度ω-氨基酸存在下,Pm-STA复合物形成的刺激导致Glu-Pg激活率增加。ω-氨基酸对纤维蛋白表面Pm-STA复合物形成的抑制作用是葡萄球菌激酶诱导的纤维蛋白溶解曲线出现长延迟期的原因。