Prothrombin clamart : prothrombin variant with defective arg 320-IIe cleavage by factor xa

An abnormal prothrombin has been detected in a 23 yr-old healthy female and her mother. Both patients appeared to be heterozygous for the abnormality, plasma prothrombin being 50 % of normal using the usual one stage assay, but normal when measured either by using Echis carinatus venom or by immunoa...

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Veröffentlicht in:Thrombosis research 1986-10, Vol.44 (1), p.11-21
Hauptverfasser: Huisse, Marie-Geneviéve, Dreyfus, Marie, Guillin, Marie-Claude
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creator Huisse, Marie-Geneviéve
Dreyfus, Marie
Guillin, Marie-Claude
description An abnormal prothrombin has been detected in a 23 yr-old healthy female and her mother. Both patients appeared to be heterozygous for the abnormality, plasma prothrombin being 50 % of normal using the usual one stage assay, but normal when measured either by using Echis carinatus venom or by immunoassay. No abnormality in the immunoelectrophoretic pattern was observed. Prothrombin isolation on DEAE Sephadex failed to separate the abnormal population (prothrombin Clamart) from the normal one. The rates of prothrombin activation by factor Xa, in the presence or absence of phospholipids and/ or factor Va, were determined by measuring the production of both clotting and amidolytic activities. The thrombin generation rate from prothrombin isolated from the propositus plasma was 50 % slower than normal whatever the method of measurement and the composition of the activation mixture. Analysis of the final activation products by SDS polyacrylamide gel electrophoresis revealed that equal amounts of prethrombin 2 and thrombin had been formed. Prethrombin 2 Clamart was shown to be resistant to proteolysis upon further incubation with factor Xa, whereas it was readily converted to thrombin by Echis carinatus venom. Prothrombin Clamart appears to be characterized by an impairment of Arg 320-IIe cleavage by factor Xa.
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Both patients appeared to be heterozygous for the abnormality, plasma prothrombin being 50 % of normal using the usual one stage assay, but normal when measured either by using Echis carinatus venom or by immunoassay. No abnormality in the immunoelectrophoretic pattern was observed. Prothrombin isolation on DEAE Sephadex failed to separate the abnormal population (prothrombin Clamart) from the normal one. The rates of prothrombin activation by factor Xa, in the presence or absence of phospholipids and/ or factor Va, were determined by measuring the production of both clotting and amidolytic activities. The thrombin generation rate from prothrombin isolated from the propositus plasma was 50 % slower than normal whatever the method of measurement and the composition of the activation mixture. Analysis of the final activation products by SDS polyacrylamide gel electrophoresis revealed that equal amounts of prethrombin 2 and thrombin had been formed. Prethrombin 2 Clamart was shown to be resistant to proteolysis upon further incubation with factor Xa, whereas it was readily converted to thrombin by Echis carinatus venom. 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Both patients appeared to be heterozygous for the abnormality, plasma prothrombin being 50 % of normal using the usual one stage assay, but normal when measured either by using Echis carinatus venom or by immunoassay. No abnormality in the immunoelectrophoretic pattern was observed. Prothrombin isolation on DEAE Sephadex failed to separate the abnormal population (prothrombin Clamart) from the normal one. The rates of prothrombin activation by factor Xa, in the presence or absence of phospholipids and/ or factor Va, were determined by measuring the production of both clotting and amidolytic activities. The thrombin generation rate from prothrombin isolated from the propositus plasma was 50 % slower than normal whatever the method of measurement and the composition of the activation mixture. Analysis of the final activation products by SDS polyacrylamide gel electrophoresis revealed that equal amounts of prethrombin 2 and thrombin had been formed. Prethrombin 2 Clamart was shown to be resistant to proteolysis upon further incubation with factor Xa, whereas it was readily converted to thrombin by Echis carinatus venom. 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Both patients appeared to be heterozygous for the abnormality, plasma prothrombin being 50 % of normal using the usual one stage assay, but normal when measured either by using Echis carinatus venom or by immunoassay. No abnormality in the immunoelectrophoretic pattern was observed. Prothrombin isolation on DEAE Sephadex failed to separate the abnormal population (prothrombin Clamart) from the normal one. The rates of prothrombin activation by factor Xa, in the presence or absence of phospholipids and/ or factor Va, were determined by measuring the production of both clotting and amidolytic activities. The thrombin generation rate from prothrombin isolated from the propositus plasma was 50 % slower than normal whatever the method of measurement and the composition of the activation mixture. Analysis of the final activation products by SDS polyacrylamide gel electrophoresis revealed that equal amounts of prethrombin 2 and thrombin had been formed. Prethrombin 2 Clamart was shown to be resistant to proteolysis upon further incubation with factor Xa, whereas it was readily converted to thrombin by Echis carinatus venom. Prothrombin Clamart appears to be characterized by an impairment of Arg 320-IIe cleavage by factor Xa.</abstract><cop>New York, NY</cop><pub>Elsevier Ltd</pub><pmid>3787558</pmid><doi>10.1016/0049-3848(86)90176-3</doi><tpages>11</tpages></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Adult
Arginine - metabolism
Biological and medical sciences
Blood Coagulation Disorders - genetics
dysprothrombinemia
Factor X - physiology
Factor Xa
Female
Genetic Variation
Hematologic and hematopoietic diseases
Heterozygote
Humans
Immunoelectrophoresis, Two-Dimensional
Medical sciences
Platelet diseases and coagulopathies
Prothrombin
Prothrombin - genetics
Prothrombin - isolation & purification
Prothrombin - metabolism
prothrombin activation
Prothrombin Time
Structure-Activity Relationship
Thrombin - analysis
Thrombin - metabolism
title Prothrombin clamart : prothrombin variant with defective arg 320-IIe cleavage by factor xa
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