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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0008109,
umls-concept:C0015491,
umls-concept:C0017262,
umls-concept:C0018270,
umls-concept:C0033621,
umls-concept:C0086418,
umls-concept:C0185117,
umls-concept:C0441513,
umls-concept:C0559956,
umls-concept:C0871161,
umls-concept:C1514562,
umls-concept:C1527177,
umls-concept:C1880389,
umls-concept:C1883204,
umls-concept:C1883221,
umls-concept:C2911684
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pubmed:issue |
3
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pubmed:dateCreated |
1994-2-28
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pubmed:abstractText |
The cDNA encoding a chimeric human protein C (PC), in which its epidermal growth factor-(EGF) like regions have been replaced with equivalent structures from human factor IX (fIX), was constructed and the gene product was expressed in human 293 cells. A molecular subpopulation of the recombinant chimeric protein (r-[PC/delta EGF-1,2/delta fIXEGF-1,2]) was purified that contained the full complement (9 residues/mol) of gamma-carboxyglutamic acid (Gla). After conversion by thrombin to its activated form (r-[APC/delta EGF-1,2/delta fIXEGF-1,2]), this latter enzyme was found to possess approximately 10% of the activity of wild-type recombinant APC (wtr-APC) in an APTT assay. In assay systems employing purified components, the activity of the mutant enzyme toward prothrombinase cofactor Va (fVa) and tenase cofactor VIII (fVIII) was approximately 30% and < 10%, respectively, of that of wtr-APC. The chimeric protein displayed full reactivity with a Ca(2+)-dependent monoclonal antibody to the Gla domain of PC, yielding a C50 for Ca2+ that was very similar to that obtained with wtr-PC (ca. 3.7 mM). Titrations of the dependency on Ca2+ of the intrinsic fluorescence of r-[PC/delta EGF-1,2/delta fIXEGF-1,2] allowed calculation of a C50 value of 0.34 mM, again very similar to that of wtr-PC. As with wtr-PC, Ca2+ inhibited the thrombin-catalyzed activation of r-[PC/delta EGF-1,2/delta fIXEGF-1,2] with aKi of 148 microM, as compared to a Ki of 125 microM for wtr-PC. At a saturating level of Ca2+, activation of r-[PC/delta EGF-1,2/delta fIXEGF-1,2/] by the thrombin/thrombomodulin (thrombin/TM) complex occurred at approximately 70% of the rate of that of wtr-PC.(ABSTRACT TRUNCATED AT 250 WORDS)
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Precursors,
http://linkedlifedata.com/resource/pubmed/chemical/Epidermal Growth Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Factor IX,
http://linkedlifedata.com/resource/pubmed/chemical/Factor VIII,
http://linkedlifedata.com/resource/pubmed/chemical/Factor Va,
http://linkedlifedata.com/resource/pubmed/chemical/Protein C,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0006-2960
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
25
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pubmed:volume |
33
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
823-31
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:8292611-Amino Acid Sequence,
pubmed-meshheading:8292611-Base Sequence,
pubmed-meshheading:8292611-Calcium,
pubmed-meshheading:8292611-Cells, Cultured,
pubmed-meshheading:8292611-Enzyme Activation,
pubmed-meshheading:8292611-Enzyme Precursors,
pubmed-meshheading:8292611-Epidermal Growth Factor,
pubmed-meshheading:8292611-Factor IX,
pubmed-meshheading:8292611-Factor VIII,
pubmed-meshheading:8292611-Factor Va,
pubmed-meshheading:8292611-Humans,
pubmed-meshheading:8292611-Kidney,
pubmed-meshheading:8292611-Molecular Sequence Data,
pubmed-meshheading:8292611-Protein C,
pubmed-meshheading:8292611-Recombinant Fusion Proteins,
pubmed-meshheading:8292611-Structure-Activity Relationship
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pubmed:year |
1994
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pubmed:articleTitle |
Construction, expression, and properties of a recombinant chimeric human protein C with replacement of its growth factor-like domains by those of human coagulation factor IX.
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pubmed:affiliation |
Department of Chemistry and Biochemistry, University of Notre Dame, Indiana 46556.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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