Ferjani Imen, Fattoum Abdellatif, Maciver Sutherland K, Bénistant Christine, Chahinian Anne, Manai Mohamed, Benyamin Yves, Roustan Claude
UMR 5539 (CNRS) Laboratoire de Motilité Cellulaire (Ecole Pratique des Hautes Etudes), Université de Montpellier 2, Place E. Bataillon, CC107, 34095 Montpellier Cedex 5, France.
Biochem J. 2006 Jun 15;396(3):461-8. doi: 10.1042/BJ20051690.
Gelsolin and calponin are well-characterized cytoskeletal proteins that are abundant and widely expressed in vertebrate tissues. It is also becoming apparent, however, that they are involved in cell signalling. In the present study, we show that gelsolin and calponin interact directly to form a high-affinity (K(d)=16 nM) 1:1 complex, by the use of fluorescent probes attached to both proteins, by affinity chromatography and by immunoprecipitation. These methods show that gelsolin can form high-affinity complexes with two calponin isoforms (basic h1 and acidic h3). They also show that gelsolin binds calponin through regions that have been identified previously as being calponin's actin-binding sites. Moreover, gelsolin does not interact with calponin while calponin is bound to F-actin. Reciprocal experiments to find calponin-binding sites on gelsolin show that these are in both the N- and C-terminal halves of gelsolin. Calponin has minimal effects on actin severing by gelsolin. In contrast, calponin markedly affects the nucleation activity of gelsolin. The maximum inhibition of nucleation by gelsolin was 50%, which was achieved with a ratio of two calponins for every gelsolin. Thus the interaction of calponin with gelsolin may play a regulatory role in the formation of actin filaments through modulation of gelsolin's actin-binding function and through the prevention of calponin's actin-binding activities.
凝溶胶蛋白和钙调蛋白是特征明确的细胞骨架蛋白,在脊椎动物组织中含量丰富且广泛表达。然而,它们参与细胞信号传导这一点也日益明显。在本研究中,我们通过使用连接到两种蛋白质上的荧光探针、亲和色谱法和免疫沉淀法表明,凝溶胶蛋白和钙调蛋白直接相互作用形成高亲和力(K(d)=16 nM)的1:1复合物。这些方法表明,凝溶胶蛋白可与两种钙调蛋白同工型(碱性h1和酸性h3)形成高亲和力复合物。它们还表明,凝溶胶蛋白通过先前已被确定为钙调蛋白肌动蛋白结合位点的区域与钙调蛋白结合。此外,当钙调蛋白与F-肌动蛋白结合时,凝溶胶蛋白不与钙调蛋白相互作用。寻找凝溶胶蛋白上钙调蛋白结合位点的反向实验表明,这些位点位于凝溶胶蛋白的N端和C端两半部分。钙调蛋白对凝溶胶蛋白切断肌动蛋白的作用最小。相反,钙调蛋白显著影响凝溶胶蛋白的成核活性。凝溶胶蛋白对成核的最大抑制率为50%,这是在每一个凝溶胶蛋白对应两个钙调蛋白的比例下实现的。因此,钙调蛋白与凝溶胶蛋白的相互作用可能通过调节凝溶胶蛋白的肌动蛋白结合功能以及通过防止钙调蛋白的肌动蛋白结合活性,在肌动蛋白丝的形成中发挥调节作用。