Calcium binding to the first EGF-like module of human factor IX in a recombinant fragment containing residues 1-85. Mutations V46E and Q50E each manifest a negligible increase in calcium affinity

Summary, in English

The first EGF-like module of human coagulation factor IX contains a single functionally important calcium ion binding site. We have now shown the dissociation constant for this site to be approximately 160 microM in a recombinant protein fragment consisting of residues 1-85 in human fIX. This represents a approximately 10-fold increase in affinity as compared with the isolated EGF module (residues 46-85). The Gla module (here with Glu instead of Gla) thus increases the affinity of the EGF module calcium ion binding site. Each of two mutations, V46E and Q50E, made to investigate whether the extra negative charge would increase the affinity of the calcium binding site manifested a negligible increase in affinity.

• Författare: Kristina Persson; Jan Astermark; I Bjork; Johan Stenflo
• Avdelning/ar: Klinisk kemi, Malmö; Institutionen för kliniska vetenskaper, Malmö
• Publiceringsår: 1998
• Språk: Engelska
• Sidor: 100-104
• Publikation/Tidskrift/Serie: FEBS Letters
• Volym: 421
• Issue: 2
• Länkar: http://dx.doi.org/10.1016/S0014-5793(97)01546-9
• Dokumenttyp: Artikel i tidskrift
• Förlag: Wiley-Blackwell
• Ämne: Biological Sciences
• Nyckelord: Site-directed mutagenesis; Human factor IX; Dissociation constant; Calcium binding; EGF-like module
• Status: Published
• Forskningsgrupp: Clinical Chemistry, Malmö
• ISBN/ISSN/Övrigt: ISSN: 1873-3468