Howard Hughes Medical Institute, University of Wisconsin, Madison, WI 53706, USA.
J Cell Biol. 2010 Oct 4;191(1):187-97. doi: 10.1083/jcb.201002089.
Otoferlin is a large multi-C2 domain protein proposed to act as a calcium sensor that regulates synaptic vesicle exocytosis in cochlear hair cells. Although mutations in otoferlin have been associated with deafness, its contribution to neurotransmitter release is unresolved. Using recombinant proteins, we demonstrate that five of the six C2 domains of otoferlin sense calcium with apparent dissociation constants that ranged from 13-25 µM; in the presence of membranes, these apparent affinities increase by up to sevenfold. Using a reconstituted membrane fusion assay, we found that five of the six C2 domains of otoferlin stimulate membrane fusion in a calcium-dependent manner. We also demonstrate that a calcium binding-deficient form of the C2C domain is incapable of stimulating membrane fusion, further underscoring the importance of calcium for the protein's function. These results demonstrate for the first time that otoferlin is a calcium sensor that can directly regulate soluble N-ethyl-maleimide sensitive fusion protein attachment protein receptor-mediated membrane fusion reactions.
耳钙蛋白是一种具有多个 C2 结构域的大型蛋白,被认为是一种钙传感器,可调节耳蜗毛细胞中突触囊泡的胞吐作用。尽管耳钙蛋白的突变与耳聋有关,但它对神经递质释放的贡献仍未得到解决。我们使用重组蛋白证明,耳钙蛋白的六个 C2 结构域中的五个能够感知钙,其表观解离常数范围为 13-25µM;在存在膜的情况下,这些表观亲和力增加了多达七倍。使用重建的膜融合测定法,我们发现耳钙蛋白的六个 C2 结构域中的五个以钙依赖性方式刺激膜融合。我们还证明,C2C 结构域的钙结合缺陷形式不能刺激膜融合,这进一步强调了钙对该蛋白功能的重要性。这些结果首次表明,耳钙蛋白是一种钙传感器,可直接调节可溶性 N-乙基-马来酰亚胺敏感的融合蛋白附着蛋白受体介导的膜融合反应。