Matches in SemOpenAlex for { <https://semopenalex.org/work/W2028213166> ?p ?o ?g. }
- W2028213166 endingPage "138" @default.
- W2028213166 startingPage "131" @default.
- W2028213166 abstract "Factor-Xa-catalyzed prothrombin activation is greatly accelerated by negatively charged phospholipids plus calcium ions. In 1990, we reported that neutral phosphatidylcholine membranes also stimulated prothrombin activation [Gerads, I., Govers-Riemslag, J.W.P., Tans, G., Zwaal, R. F. A. & Rosing, J. (1990) Biochemistry 29, 7967-7974]. In the present study, we have performed a detailed analysis of the prothrombin-converting activity of phosphatidylcholine membranes. Stimulation of prothrombin activation by phosphatidylcholine vesicles was particularly observed (a) with phosphatidylcholine molecules that contained unsaturated hydrocarbon side chains, (b) in the presence of factor Va, (c) at low ionic strength and (d) when Ca2+ were present in the reaction medium. It is unlikely that the prothrombinase activity of phosphatidylcholine preparations was due to contaminating anionic phospholipids. This is concluded from the fact that thin-layer chromatographic analysis showed that dioleoylphosphatidylcholine [(Ole)2GroPCho] contained less than 0.1 mol/100 mol anionic phospholipid, and that incorporation of such amounts of anionic lipids in (Ole)2-GroPCho membranes hardly increased their prothrombin-converting activity. At low ionic strength and in the presence of factor Va and Ca2+ (Ole)2GroPCho membranes accelerated prothrombin activation about 100-fold. At ionic strength (I) 0.06, prothrombin activation on 100 microM (Ole)2-GroPCho was characterized by a Km for prothrombin of 2 microM, a Vmax of 3020 IIa min-1.Xa-1 and a Kd for factor XaVa complex formation at the membrane surface of 7.5 nM. Prothrombin activation on (Ole)2GroPCho membranes was drastically reduced when the ionic strength was increased. The inhibition at high ionic strength could be explained by an effect on the Kd for XaVa complex formation which increased from 7.5 nM at I = 0.06 to 100 nM at I = 0.22. Prothrombin activation on (Ole)2GroPCho required Ca2+ and was dependent on the presence of gamma-carboxyglutamic acid domains in prothrombin and factor Xa. This indicates that similar interactions may account for the assembly of prothrombinase complexes on phosphatidylcholine and an anionic lipid-containing membranes." @default.
- W2028213166 created "2016-06-24" @default.
- W2028213166 creator A5026953664 @default.
- W2028213166 creator A5053372098 @default.
- W2028213166 creator A5069031083 @default.
- W2028213166 creator A5087919219 @default.
- W2028213166 date "1994-02-01" @default.
- W2028213166 modified "2023-10-17" @default.
- W2028213166 title "Prothrombin activation on dioleoylphosphatidylcholine membranes" @default.
- W2028213166 cites W123355458 @default.
- W2028213166 cites W1480892540 @default.
- W2028213166 cites W1490507833 @default.
- W2028213166 cites W1505723334 @default.
- W2028213166 cites W1508750197 @default.
- W2028213166 cites W1514670886 @default.
- W2028213166 cites W1516041101 @default.
- W2028213166 cites W1531765158 @default.
- W2028213166 cites W1545184091 @default.
- W2028213166 cites W1547867352 @default.
- W2028213166 cites W1581065702 @default.
- W2028213166 cites W1603919509 @default.
- W2028213166 cites W1782728159 @default.
- W2028213166 cites W1961597147 @default.
- W2028213166 cites W1972594540 @default.
- W2028213166 cites W1975525211 @default.
- W2028213166 cites W1991651684 @default.
- W2028213166 cites W2001859902 @default.
- W2028213166 cites W2011105427 @default.
- W2028213166 cites W2016445477 @default.
- W2028213166 cites W2026360066 @default.
- W2028213166 cites W2049506738 @default.
- W2028213166 cites W2050332662 @default.
- W2028213166 cites W2051441143 @default.
- W2028213166 cites W2065156100 @default.
- W2028213166 cites W2072395307 @default.
- W2028213166 cites W2076876900 @default.
- W2028213166 cites W2079454393 @default.
- W2028213166 cites W2091317550 @default.
- W2028213166 cites W2093111323 @default.
- W2028213166 cites W2097993282 @default.
- W2028213166 cites W2105944387 @default.
- W2028213166 cites W2126206535 @default.
- W2028213166 cites W2170055916 @default.
- W2028213166 cites W62994428 @default.
- W2028213166 doi "https://doi.org/10.1111/j.1432-1033.1994.tb18607.x" @default.
- W2028213166 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/8119280" @default.
- W2028213166 hasPublicationYear "1994" @default.
- W2028213166 type Work @default.
- W2028213166 sameAs 2028213166 @default.
- W2028213166 citedByCount "18" @default.
- W2028213166 crossrefType "journal-article" @default.
- W2028213166 hasAuthorship W2028213166A5026953664 @default.
- W2028213166 hasAuthorship W2028213166A5053372098 @default.
- W2028213166 hasAuthorship W2028213166A5069031083 @default.
- W2028213166 hasAuthorship W2028213166A5087919219 @default.
- W2028213166 hasConcept C112516734 @default.
- W2028213166 hasConcept C12554922 @default.
- W2028213166 hasConcept C130316041 @default.
- W2028213166 hasConcept C178790620 @default.
- W2028213166 hasConcept C184651966 @default.
- W2028213166 hasConcept C185592680 @default.
- W2028213166 hasConcept C187428577 @default.
- W2028213166 hasConcept C203014093 @default.
- W2028213166 hasConcept C2776330855 @default.
- W2028213166 hasConcept C2777292125 @default.
- W2028213166 hasConcept C2778918659 @default.
- W2028213166 hasConcept C41625074 @default.
- W2028213166 hasConcept C43617362 @default.
- W2028213166 hasConcept C55493867 @default.
- W2028213166 hasConcept C86803240 @default.
- W2028213166 hasConcept C89560881 @default.
- W2028213166 hasConceptScore W2028213166C112516734 @default.
- W2028213166 hasConceptScore W2028213166C12554922 @default.
- W2028213166 hasConceptScore W2028213166C130316041 @default.
- W2028213166 hasConceptScore W2028213166C178790620 @default.
- W2028213166 hasConceptScore W2028213166C184651966 @default.
- W2028213166 hasConceptScore W2028213166C185592680 @default.
- W2028213166 hasConceptScore W2028213166C187428577 @default.
- W2028213166 hasConceptScore W2028213166C203014093 @default.
- W2028213166 hasConceptScore W2028213166C2776330855 @default.
- W2028213166 hasConceptScore W2028213166C2777292125 @default.
- W2028213166 hasConceptScore W2028213166C2778918659 @default.
- W2028213166 hasConceptScore W2028213166C41625074 @default.
- W2028213166 hasConceptScore W2028213166C43617362 @default.
- W2028213166 hasConceptScore W2028213166C55493867 @default.
- W2028213166 hasConceptScore W2028213166C86803240 @default.
- W2028213166 hasConceptScore W2028213166C89560881 @default.
- W2028213166 hasIssue "1" @default.
- W2028213166 hasLocation W20282131661 @default.
- W2028213166 hasLocation W20282131662 @default.
- W2028213166 hasOpenAccess W2028213166 @default.
- W2028213166 hasPrimaryLocation W20282131661 @default.
- W2028213166 hasRelatedWork W1876125771 @default.
- W2028213166 hasRelatedWork W1965990791 @default.
- W2028213166 hasRelatedWork W1971257644 @default.
- W2028213166 hasRelatedWork W1979035221 @default.
- W2028213166 hasRelatedWork W2060060915 @default.
- W2028213166 hasRelatedWork W2063810897 @default.