Leukert Nadja, Vogl Thomas, Strupat Kerstin, Reichelt Rudolf, Sorg Clemens, Roth Johannes
Institute of Experimental Dermatology, University of Muenster, Roentgenstr. 21, 48149 Muenster, Germany.
J Mol Biol. 2006 Jun 16;359(4):961-72. doi: 10.1016/j.jmb.2006.04.009. Epub 2006 Apr 21.
S100 proteins comprise the largest family of calcium-binding proteins. Members of this family usually form homo- or heterodimers, which may associate to higher-order oligomers in a calcium-dependent manner. The heterodimers of S100A8 and S100A9 represent the major calcium-binding proteins in phagocytes. Both proteins regulate migration of these cells via modulation of tubulin polymerization. Calcium binding induces formation of (S100A8/S100A9)2 tetramers. The functional relevance of these higher-order oligomers of S100 proteins, however, is not yet clear. To investigate the importance of higher-order oligomerization for S100 proteins, we created a set of mutations within S100A9 (N69A, E78A, N69A+E78A) destroying the high-affinity C-terminal calcium-binding site (EF-hand II). Mutations in EF-hand II did not interfere with formation of the S100A8/S100A9 heterodimer as demonstrated by yeast two-hybrid experiments and pull-down assays. In contrast, mass spectrometric analysis and density gradient centrifugation revealed that calcium-induced association of (S100A8/S100A9)2 tetramers was strictly dependent on a functional EF-hand II in S100A9. Failure of tetramer formation was associated with a lack of functional activity of S100A8/S100A9 complexes in promoting the formation of microtubules. Thus, our data demonstrate that calcium-dependent formation of (S100A8/S100A9)2 tetramers is an essential prerequisite for biological function. This is the first report showing a functional relevance of calcium-induced higher-order oligomerization in the S100 family.
S100蛋白构成了最大的钙结合蛋白家族。该家族成员通常形成同二聚体或异二聚体,它们可能以钙依赖的方式缔合形成高阶寡聚体。S100A8和S100A9的异二聚体是吞噬细胞中的主要钙结合蛋白。这两种蛋白都通过调节微管蛋白聚合来调控这些细胞的迁移。钙结合诱导(S100A8/S100A9)2四聚体的形成。然而,这些S100蛋白高阶寡聚体的功能相关性尚不清楚。为了研究高阶寡聚化对S100蛋白的重要性,我们在S100A9内创建了一组突变(N69A、E78A、N69A+E78A),破坏了高亲和力的C端钙结合位点(EF手型结构域II)。酵母双杂交实验和下拉分析表明,EF手型结构域II中的突变不影响S100A8/S100A9异二聚体的形成。相反,质谱分析和密度梯度离心显示,钙诱导的(S100A8/S100A9)2四聚体缔合严格依赖于S100A9中功能性的EF手型结构域II。四聚体形成失败与S100A8/S100A9复合物促进微管形成的功能活性缺失有关。因此,我们的数据表明,(S100A8/S100A9)2四聚体的钙依赖性形成是生物学功能的必要前提。这是第一份显示S100家族中钙诱导的高阶寡聚化具有功能相关性的报告。