Kozlov L V, Rostovtseva L I, Lomaka T S, Sutovskaia N S
Bioorg Khim. 1985 Jun;11(6):762-8.
Various nucleophilic agents (acceptors) react with thiolester group of nascent activated fragment (C3b) of the third complement component. The C3b-acceptors binding prevents transformation of C3 convertase to C5 convertase and results in inhibition of the cell-target lysis. A convenient method of monitoring the EAC142 to EAC1423 transformation was elaborated. Character of the inhibition suggests that the covalent binding follows a stage of the reversible C3b-acceptor complex formation. The method allows to determine the maximum of inhibition of the C5 convertase formation and the dissociation constant of the reversible C3b-acceptor complex, which reflects the C3b affinity to this acceptor.
各种亲核试剂(受体)与第三补体成分新生活化片段(C3b)的硫酯基团发生反应。C3b与受体的结合可阻止C3转化酶转变为C5转化酶,并导致细胞靶裂解受到抑制。一种监测EAC142向EAC1423转化的简便方法得以完善。抑制作用的特点表明,共价结合发生在可逆的C3b-受体复合物形成阶段之后。该方法能够确定C5转化酶形成的最大抑制程度以及可逆C3b-受体复合物的解离常数,后者反映了C3b对该受体的亲和力。