Literature DB >> 7592932

Prothrombin contributes to the assembly of the factor Va-factor Xa complex at phosphatidylserine-containing phospholipid membranes.

D Billy1, G M Willems, H C Hemker, T Lindhout.   

Abstract

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.

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Year:  1995        PMID: 7592932     DOI: 10.1074/jbc.270.45.26883

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  6 in total

1.  Prothrombin kringle 1 domain interacts with factor Va during the assembly of prothrombinase complex.

Authors:  H Deguchi; H Takeya; E C Gabazza; J Nishioka; K Suzuki
Journal:  Biochem J       Date:  1997-02-01       Impact factor: 3.857

2.  Notecarin D binds human factor V and factor Va with high affinity in the absence of membranes.

Authors:  Jennifer L Newell-Caito; Malabika Laha; Anthony C Tharp; Jonathan I Creamer; Hong Xu; Ashoka A Maddur; Guido Tans; Paul E Bock
Journal:  J Biol Chem       Date:  2011-09-12       Impact factor: 5.157

3.  Modulation of prothrombinase assembly and activity by phosphatidylethanolamine.

Authors:  Rinku Majumder; Xiaoe Liang; Mary Ann Quinn-Allen; William H Kane; Barry R Lentz
Journal:  J Biol Chem       Date:  2011-08-22       Impact factor: 5.157

4.  Crystal structure of the bovine lactadherin C2 domain, a membrane binding motif, shows similarity to the C2 domains of factor V and factor VIII.

Authors:  Lin Lin; Qing Huai; Mingdong Huang; Bruce Furie; Barbara C Furie
Journal:  J Mol Biol       Date:  2007-05-25       Impact factor: 5.469

5.  Identification and characterization of a factor Va-binding site on human prothrombin fragment 2.

Authors:  Alexander P Friedmann; Anatoli Koutychenko; Chengliang Wu; James C Fredenburgh; Jeffrey I Weitz; Peter L Gross; Ping Xu; Feng Ni; Paul Y Kim
Journal:  Sci Rep       Date:  2019-02-21       Impact factor: 4.379

6.  Phosphatidylethanolamine critically supports internalization of cell-penetrating protein C inhibitor.

Authors:  Petra Baumgärtner; Margarethe Geiger; Susanne Zieseniss; Julia Malleier; James A Huntington; Karin Hochrainer; Edith Bielek; Mechthild Stoeckelhuber; Kirsten Lauber; Dag Scherfeld; Petra Schwille; Katja Wäldele; Klaus Beyer; Bernd Engelmann
Journal:  J Cell Biol       Date:  2007-11-19       Impact factor: 10.539

  6 in total

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