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S100A8和S100A9依赖钙的四聚体形成对于生物活性至关重要。

Calcium-dependent tetramer formation of S100A8 and S100A9 is essential for biological activity.

作者信息

Leukert Nadja, Vogl Thomas, Strupat Kerstin, Reichelt Rudolf, Sorg Clemens, Roth Johannes

机构信息

Institute of Experimental Dermatology, University of Muenster, Roentgenstr. 21, 48149 Muenster, Germany.

出版信息

J Mol Biol. 2006 Jun 16;359(4):961-72. doi: 10.1016/j.jmb.2006.04.009. Epub 2006 Apr 21.

Abstract

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.

摘要

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。

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