Lenting P J, van de Loo J W, Donath M J, van Mourik J A, Mertens K
Department of Blood Coagulation, Central Laboratory of the Netherlands Red Cross Blood Transfusion Service, Amsterdam, The Netherlands.
J Biol Chem. 1996 Jan 26;271(4):1935-40. doi: 10.1074/jbc.271.4.1935.
In previous studies have shown that the interaction between factor IXa and VIII involves the light chain of factor VIII and that this interaction inhibited by the monoclonal antibody CLB-CAg A against the factor VIII region Gln1778-Asp1840 (Lenting, P.J., Donath, M.J.S.H., van Mourik, J.A., and Mertens, K. (1994) J. Biol. Chem. 269, 7150-7155). Employing distinct recombinant factor VIII fragments, we now have localized the epitope of this antibody more precisely between the A3 domain residues Glu1801 and Met1823. Hydropathy analysis indicated that this region is part of a major hydrophilic exosite within the A3 domain. The interaction of factor IXa with this exosite was studied by employing overlapping synthetic peptides encompassing the factor VII region Tyr1786-Ala1834. Factor IXa binding was found to be particularly efficient to peptide corresponding to the factor VIII sequences Lys1804-Lys1818 and Glu1811-Gln1820. The same peptides proved effective in binding antibody CLB-CAg A. Further analysis revealed that peptides Lys1804-Lys1818 and Glu1811-Gln1820 interfere with binding of factor IXa to immobilized factor VIII light chain (Ki approximately 0.2 mM and 0.3 mM, respectively). Moreover, these peptides inhibit factor X activation by factor IXa in the presence of factor VIIIa (Ki approximately 0.2 mM and 0.3 mM, respectively) but not in its absence. Equilibrium binding studies revealed that these two peptides bind to the factor IX zymogen and its activated form, factor IXa, with the same affinity (apparent Kd approximately 0.2 mM), whereas the complete factor VIII light chain displays preferential binding to factor IXa. In conclusion, our results demonstrate that peptides consisting of the factor VIII light chain residues Lys1804-Lys1818 and Glu1811-Gln1820 share a factor IXa binding site that is essential for the assembly of the factor X-activating factor IXa-factor VIIIa complex. We propose that the overlapping sequence Glu1811-Lys1818 comprises the minimal requirements for binding to activated factor IX.
先前的研究表明,因子IXa与因子VIII之间的相互作用涉及因子VIII的轻链,并且这种相互作用被针对因子VIII区域Gln1778 - Asp1840的单克隆抗体CLB - CAg A所抑制(Lenting, P.J., Donath, M.J.S.H., van Mourik, J.A., and Mertens, K. (1994) J. Biol. Chem. 269, 7150 - 7155)。利用不同的重组因子VIII片段,我们现在更精确地将该抗体的表位定位在A3结构域残基Glu1801和Met1823之间。亲水性分析表明,该区域是A3结构域内一个主要亲水性外部位点的一部分。通过使用涵盖因子VIII区域Tyr1786 - Ala1834的重叠合成肽来研究因子IXa与该外部位点的相互作用。发现因子IXa与对应于因子VIII序列Lys1804 - Lys1818和Glu1811 - Gln1820的肽结合特别有效。相同的肽被证明能有效结合抗体CLB - CAg A。进一步分析表明,肽Lys1804 - Lys1818和Glu1811 - Gln1820干扰因子IXa与固定化因子VIII轻链的结合(Ki分别约为0.2 mM和0.3 mM)。此外,在因子VIIIa存在的情况下,这些肽抑制因子IXa对因子X的激活(Ki分别约为0.2 mM和0.3 mM),但在其不存在时则不然。平衡结合研究表明,这两种肽以相同的亲和力(表观Kd约为0.2 mM)结合因子IX酶原及其活化形式因子IXa,而完整的因子VIII轻链则优先结合因子IXa。总之,我们的结果表明,由因子VIII轻链残基Lys1804 - Lys1818和Glu1811 - Gln1820组成的肽共享一个因子IXa结合位点,该位点对于因子X激活因子IXa - 因子VIIIa复合物的组装至关重要。我们提出,重叠序列Glu1811 - Lys1818包含与活化因子IX结合的最低要求。