Relationship between the binding sites for von Willebrand factor, phospholipid, and human factor VIII C2 inhibitor alloantibodies within the factor VIII C2 domain

• Published in: International journal of hematology 2007-05, Vol.85 (4), p.317-322
• Main Authors: NOGAMI, Keiji, SHIMA, Midori, GIDDINGS, John C, TAKEYAMA, Masahiro, TANAKA, Ichiro, YOSHIOKA, Akira
• Format: Article
• Language: English
• Subjects: Amino Acid Substitution - immunology; Binding Sites - genetics; Binding Sites - immunology; Biological and medical sciences; Blood Coagulation Factor Inhibitors - immunology; Epitope Mapping; Factor VIII - genetics; Factor VIII - immunology; Hematologic and hematopoietic diseases; Humans; Isoantibodies - immunology; Medical sciences; Mutation, Missense - immunology; Phospholipids - immunology; Protein Structure, Tertiary - genetics; von Willebrand Factor - immunology
• ISSN: 0925-5710; 1865-3774
• DOI: 10.1532/ijh97.06192

Some factor VIII (FVIII) inhibitor alloantibodies block FVIII binding to von Willebrand factor (VWF) and phospholipid (PL) and recognize a C2 domain epitope that overlaps both binding sites. We previously showed that FVIII peptide 2315-2330 neutralized FVIII inhibitors and that Cys2326 and Glu2327 contributed to the maximum neutralizing effect. In the present study, we investigated the relationship between the essential binding sites for VWF, PL, and anti-C2 inhibitors by means of competitive-inhibition assays with overlapping synthetic peptides that span the C terminus of the C2 domain (residues 2288-2332). We identified 2 peptides (residues 2303-2317 and 2315-2330) that specifically blocked FVIII binding to VWF or PL by approximately 80% (50%-inhibitory concentration [IC50], 9.0 microM) and 95% (IC50, 0.12 microM), respectively. To examine in detail the residues responsible for PL binding, we prepared mutants of peptide 2315-2330 in which we sequentially substituted each residue with Gly. Two residues, Ile2317 and Met2321, were shown to be essential for PL binding. Their substitution with Gly reduced the inhibitory effect by >90%. The data suggest that the binding sites for VWF, PL, and anti-C2 inhibitors in the C2 domain are in very close proximity but are not identical.