Literature DB >> 3113477

Acceleration of surface-dependent autocatalytic activation of blood coagulation factor XII by divalent metal ions.

J D Shore, D E Day, P E Bock, S T Olson.   

Abstract

The effect of divalent metal ions on the rate of dextran sulfate dependent autocatalytic activation of human blood coagulation factor XII was studied at pH 7.4 and 25 degrees C. Zn2+ and Cu2+, but not Co2+, increased the rate of factor XII activation induced by dextran sulfate with optimum effects at approximately 5 and 1 microM, respectively, while Ca2+ acceleration required much higher concentrations (millimolar). Further investigation of the effect of Zn2+ on factor XII activation demonstrated a complete dependence on the presence of dextran sulfate, lack of inhibition by soybean trypsin inhibitor, the appearance of alpha-XIIa as the primary reaction product, and reaction kinetics characteristic of an autocatalytic process. These results were consistent with Zn2+ affecting only the rate of surface-mediated factor XII autoactivation. The initial turnover velocity of dextran sulfate induced factor XII autoactivation increased linearly with factor XII concentration in the absence of Zn2+ up to 0.9 microM factor XII but showed saturation behavior over this same concentration range in the presence of 5 microM Zn2+, indicating that Zn2+ increased the reaction rate primarily by lowering the apparent Km. Comparison of the kinetics of autoactivation at mu = 0.15 and 0.24 revealed that the enhancement in the apparent kcat/Km brought about by Zn2+ increased from 19-fold to 520-fold, respectively, due to a differential dependence of the Zn2+-stimulated and unstimulated reactions on ionic strength.(ABSTRACT TRUNCATED AT 250 WORDS)

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3113477     DOI: 10.1021/bi00382a027

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  6 in total

1.  Binding of Zn2+ to a Ca2+ loop allosterically attenuates the activity of factor VIIa and reduces its affinity for tissue factor.

Authors:  L C Petersen; O H Olsen; L S Nielsen; P O Freskgård; E Persson
Journal:  Protein Sci       Date:  2000-05       Impact factor: 6.725

2.  Zinc chelation promotes streptokinase-induced thrombolysis in vitro.

Authors:  Zihui Wang; Xinge Yu; Yang V Li
Journal:  Int J Physiol Pathophysiol Pharmacol       Date:  2017-11-01

3.  Zinc modulates the interaction of protein C and activated protein C with endothelial cell protein C receptor.

Authors:  Prosenjit Sen; Sanghamitra Sahoo; Usha R Pendurthi; L Vijaya Mohan Rao
Journal:  J Biol Chem       Date:  2010-04-22       Impact factor: 5.157

4.  Polyphosphate colocalizes with factor XII on platelet-bound fibrin and augments its plasminogen activator activity.

Authors:  Joanne L Mitchell; Ausra S Lionikiene; Georgi Georgiev; Anja Klemmer; Chelsea Brain; Paul Y Kim; Nicola J Mutch
Journal:  Blood       Date:  2016-09-30       Impact factor: 22.113

5.  Dietary zinc depletion and repletion affects plasma proteins: an analysis of the plasma proteome.

Authors:  Arthur Grider; Kathie Wickwire; Emily Ho; Carolyn S Chung; Janet King
Journal:  Biometals       Date:  2012-12-20       Impact factor: 2.949

6.  Immobilized transition metal ions stimulate contact activation and drive factor XII-mediated coagulation.

Authors:  N J Mutch; E K Waters; J H Morrissey
Journal:  J Thromb Haemost       Date:  2012-10       Impact factor: 5.824

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.