Kilchherr E, Fuchs H, Tschopp J, Engel J
Mol Immunol. 1982 May;19(5):683-91. doi: 10.1016/0161-5890(82)90370-4.
The activation of the zymogen C1s to the enzyme C1s in the human C1 complex [C1q(c1rC1s)2] was studied as a function of the concentrations of (C1rC1s)2 and C1q which were saturated with oligomers of rabbit IgG. A large concentration dependence of the sigmoidal kinetics was observed in the 2-180 nM concentration range. This was explained by association-dissociation equilibria between the antibody-saturated C1q and various forms of the (C1rC1s)2 complex (unactivated to activated). The establishment of these equilibria (binding constant 2 x 10(7) M-1) was assumed to be fast as compared to the rates of the activation steps (rate constants 10(-3) and 10(-2) sec-1 at 30 degrees C). The fast re-equilibration of the C1 complex explains the finding that small amounts of antibody-saturated C1q catalysed the activation of large amounts of C1s. The interpretation of the kinetic results was supported by a direct demonstration of the dissociation of C1 into C1q and (C1rC1s)2 by analytical and density gradient centrifugation. No difference was found between the rates of activation and the dissociation properties of reconstituted C1 and C1 isolated from serum.
在人C1复合物[C1q(c1rC1s)2]中,研究了酶原C1s向酶C1的激活过程,该过程是兔IgG寡聚体饱和的(C1rC1s)2和C1q浓度的函数。在2 - 180 nM浓度范围内观察到S形动力学对浓度有很大依赖性。这是由抗体饱和的C1q与(C1rC1s)2复合物的各种形式(未激活到激活)之间的缔合 - 解离平衡所解释的。与激活步骤的速率(30℃时速率常数为10(-3)和10(-2)秒-1)相比,这些平衡(结合常数2×10(7) M-1)的建立被认为是快速的。C1复合物的快速重新平衡解释了少量抗体饱和的C1q能催化大量C1s激活这一发现。通过分析超速离心和密度梯度离心直接证明C1解离为C1q和(C1rC1s)2,支持了动力学结果的解释。重组C1与从血清中分离的C1在激活速率和解离特性方面未发现差异。