A hydrophobic patch (PLVIVG; 1481-1486) in the B-domain of factor V-short is crucial for its synergistic TFPIα-cofactor activity with protein S and for the formation of the FXa-inhibitory complex comprising FV-short, TFPIα, and protein S

被引:14
作者
Dahlback, Bjorn [1 ]
Tran, Sinh [1 ]
机构
[1] Lund Univ, Univ Hosp, Dept Translat Med, Malmo, Sweden
关键词
blood coagulation; factor V; factor Xa; protein S; tissue factor pathway inhibitor; TISSUE FACTOR PATHWAY; PROTHROMBINASE; COAGULATION; PROTEOLYSIS; INITIATION; REGION;
D O I
10.1111/jth.15690
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Factor V-short (FV756-1458) is a natural splice variant functioning in synergy with protein S as tissue factor pathway inhibitor alpha (TFPI alpha)-cofactor in inhibition of factor Xa (FXa). An exposed acid region (AR2; 1493-1537) in the B domain binds TFPI alpha. The preAR2 (1458-1492) is crucial for the synergistic TFPI alpha-cofactor activity between FV-short and protein S and for assembly of a trimolecular FXa-inhibitory complex among FV-short, protein S, and TFPI alpha. Objective To identify which part of preAR2 is required for the synergistic TFPI alpha-cofactor activity between FV-short and protein S. Methods A FXa-inhibition assay was used to test the synergistic TFPI alpha cofactor activity between protein S and new FV-short variants FV709-1476, FV712-1478, FV712-1481, FV712-1484, FV712-1487, and FV712-1490. A microtiter-based assay analyzed binding among FV-short variants, protein S, and TFPI alpha. Results FV709-1476, FV712-1478, and FV712-1481 were fully active as synergistic TFPI alpha cofactors with protein S; FV712-1484 showed intermediate activity; and FV712-1487 and FV712-1490 were inactive. TFPI alpha interacted with all variants in the absence of protein S but FV712-1478 and FV712-1481 bound TFPI alpha with highest affinity. None of the FV-short variants bound directly to protein S in the absence of TFPI alpha. In the presence of TFPI alpha, efficient cooperative binding was demonstrated between protein S, TFPI alpha, and FV709-1476, FV712-1478, or FV712-1481. In contrast, no cooperativity among TFPI alpha, protein S, and FV712-1484, FV712-1487, or FV712-1490 was seen. Conclusion A short hydrophobic patch in preAR2 (PLVIVG, 1481-1486) in FV-short is crucial for the synergistic TFPI alpha-cofactor activity between FV-short and protein S and for the assembly of a trimolecular FXa-inhibitory complex among FV-short, protein S, and TFPI alpha.
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页码:1146 / 1157
页数:12
相关论文
共 36 条
[1]   Identification of functionally important residues in TFPI Kunitz domain 3 required for the enhancement of its activity by protein S [J].
Ahnstroem, Josefin ;
Andersson, Helena M. ;
Hockey, Verity ;
Meng, Yiran ;
McKinnon, Thomas A. J. ;
Hamuro, Tsutomu ;
Crawley, James T. B. ;
Lane, David A. .
BLOOD, 2012, 120 (25) :5059-5062
[2]   A Bipartite Autoinhibitory Region within the B-domain Suppresses Function in Factor V [J].
Bos, Mettine H. A. ;
Camire, Rodney M. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (31) :26342-26351
[3]   Tissue factor pathway inhibitor: structure-function [J].
Broze, George J., Jr. ;
Girard, Thomas J. .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2012, 17 :262-280
[4]   Restoring the Procofactor State of Factor Va-like Variants by Complementation with B-domain Peptides [J].
Bunce, Matthew W. ;
Bos, Mettine H. A. ;
Krishnaswamy, Sriram ;
Camire, Rodney M. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2013, 288 (42) :30151-30160
[5]   Rethinking events in the haemostatic process: role of factor V and TFPI [J].
Camire, R. M. .
HAEMOPHILIA, 2016, 22 :3-8
[6]   The molecular basis of factor V and VIII procofactor activation [J].
Camire, R. M. ;
Bos, M. H. A. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2009, 7 (12) :1951-1961
[7]   A novel mutation in the F5 gene (factor V Amsterdam) associated with bleeding independent of factor V procoagulant function [J].
Cunha, Marisa L. R. ;
Bakhtiari, Kamran ;
Peter, Jorge ;
Marquart, J. Arnoud ;
Meijers, Joost C. M. ;
Middeldorp, Saskia .
BLOOD, 2015, 125 (11) :1822-1825
[8]   PURIFICATION OF HUMAN VITAMIN-K-DEPENDENT PROTEIN-S AND ITS LIMITED PROTEOLYSIS BY THROMBIN [J].
DAHLBACK, B .
BIOCHEMICAL JOURNAL, 1983, 209 (03) :837-846
[9]   Blood coagulation [J].
Dahlback, B .
LANCET, 2000, 355 (9215) :1627-1632
[10]   Novel insights into the regulation of coagulation by factor V isoforms, tissue factor pathway inhibitorα, and protein S [J].
Dahlback, B. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2017, 15 (07) :1241-1250