Billy D, Willems G M, Hemker H C, Lindhout T
Department of Biochemistry, Cardiovascular Research Institute Maastricht, University of Limburg, The Netherlands.
J Biol Chem. 1995 Nov 10;270(45):26883-9. doi: 10.1074/jbc.270.45.26883.
The activation of prothrombin is catalyzed by prothrombinase, a complex of factor Xa and factor Va assembled on a negatively charged phospholipid membrane. We used a tubular flow reactor to identify the relative contributions of factor Va, prothrombin, and the negatively charged phosphatidylserine to the assembly of prothrombinase. Perfusion of phospholipid-coated capillaries with a mixture of factor Xa, factor Va, and prothrombin resulted in a steady-state rate of thrombin production that increased with (i) the phosphatidylserine content of the phospholipid bilayer, (ii) the factor Va concentration, and, most interestingly, (iii) the prothrombin concentration of the perfusion solution. Incorporation of 20 mol % phosphoatidylethanolamine, a phospholipid with poor ability to promote prothrombinase activity, into a 5 mol % phosphatidylserine membrane also increased the steady-state rate of thrombin production. Direct measurements of the amount of prothrombinase in the flow reactor demonstrated that increased catalytic activities were the result of an increased steady-state amount of membrane-associated prothrombinase. Thus, similar turnover numbers of prothrombin activation (3100 min-1) were calculated, irrespective of the phosphatidylserine content of the membrane. We established for membranes with low phosphatidylserine content (< 10 mol%) a linear relationship between the prothrombinase activity and the arithematical product of the factor Va concentration in the perfusion solution and the prothrombin concentration near the catalytic surface. Our results indicate that, in addition to factor Va, prothrombin also is essential to the assembly of prothrombinase at macroscopic surfaces with low phosphatidylserine content. The data further suggest that the prothrombin concentration near the surface, controlled by the prothrombinase activity and mass transfer, is an important regulator of the prothrombinase surface density.
凝血酶原的激活由凝血酶原酶催化,凝血酶原酶是由Xa因子和Va因子在带负电荷的磷脂膜上组装而成的复合物。我们使用管式流动反应器来确定Va因子、凝血酶原和带负电荷的磷脂酰丝氨酸对凝血酶原酶组装的相对贡献。用Xa因子、Va因子和凝血酶的混合物灌注磷脂包被的毛细血管,导致凝血酶产生的稳态速率随着以下因素增加:(i)磷脂双层的磷脂酰丝氨酸含量;(ii)Va因子浓度,最有趣的是,(iii)灌注溶液中的凝血酶原浓度。将20 mol%的磷脂酰乙醇胺(一种促进凝血酶原酶活性能力较差的磷脂)掺入5 mol%的磷脂酰丝氨酸膜中,也增加了凝血酶产生的稳态速率。对流动反应器中凝血酶原酶量的直接测量表明,催化活性的增加是膜结合凝血酶原酶稳态量增加的结果。因此,无论膜的磷脂酰丝氨酸含量如何,计算出的凝血酶原激活的周转数相似(3100 min-1)。我们发现,对于磷脂酰丝氨酸含量低(<10 mol%)的膜,凝血酶原酶活性与灌注溶液中Va因子浓度和催化表面附近凝血酶原浓度的算术乘积之间存在线性关系。我们的结果表明,除了Va因子外,凝血酶原对于在磷脂酰丝氨酸含量低的宏观表面上凝血酶原酶的组装也至关重要。数据进一步表明,由凝血酶原酶活性和传质控制的表面附近凝血酶原浓度是凝血酶原酶表面密度的重要调节因子。