UMR 5561 CNRS, Biogéosciences, Dijon, France.
FEBS J. 2011 Jun;278(12):2117-30. doi: 10.1111/j.1742-4658.2011.08129.x. Epub 2011 May 17.
In molluscs, and more generally in metazoan organisms, the production of a calcified skeleton is a complex molecular process that is regulated by the secretion of an extracellular organic matrix. This matrix constitutes a cohesive and functional macromolecular assemblage, containing mainly proteins, glycoproteins and polysaccharides that, together, control the biomineral formation. These macromolecules interact with the extruded precursor mineral ions, mainly calcium and bicarbonate, to form complex organo-mineral composites of well-defined microstructures. For several reasons related to its remarkable mechanical properties and to its high value in jewelry, nacre is by far the most studied molluscan shell microstructure and constitutes a key model in biomineralization research. To understand the molecular mechanism that controls the formation of the shell nacreous layer, we have investigated the biochemistry of Nautilin-63, one of the main nacre matrix proteins of the cephalopod Nautilus macromphalus. After purification of Nautilin-63 by preparative electrophoresis, we demonstrate that this soluble protein is glycine-aspartate-rich, that it is highly glycosylated, that its sugar moieties are acidic, and that it is able to bind chitin in vitro. Interestingly, Nautilin-63 strongly interacts with the morphology of CaCO(3) crystals precipitated in vitro but, unexpectedly, it exhibits an extremely weak ability to inhibit in vitro the precipitation of CaCO(3) . The partial resolution of its amino acid sequence by de novo sequencing of its tryptic peptides indicates that Nautilin-63 exhibits short collagenous-like domains. Owing to specific polyclonal antibodies raised against the purified protein, Nautilin-63 was immunolocalized mainly in the intertabular nacre matrix. In conclusion, Nautilin-63 exhibits 'hybrid' biochemical properties that are found both in the soluble and insoluble proteins, rendering it difficult to classify according to the standard view on nacre proteins.
The protein sequences of N63 appear on the UniProt Knowledgebase under accession number P86702.
在软体动物中,更普遍地在后生动物中,产生钙化骨骼是一个复杂的分子过程,受细胞外有机基质的分泌调控。该基质构成一个有凝聚力和功能性的大分子组装体,主要包含蛋白质、糖蛋白和多糖,这些共同控制着生物矿化的形成。这些大分子与挤出的前体矿物质离子(主要是钙和碳酸氢盐)相互作用,形成具有明确微观结构的复杂有机-矿物复合材料。由于与出色的机械性能和高价值珠宝相关的几个原因,珍珠母迄今为止是最受研究的软体动物贝壳微结构,也是生物矿化研究的关键模型。为了理解控制贝壳珍珠层形成的分子机制,我们研究了头足类动物鹦鹉螺大蜗牛的主要珍珠母基质蛋白之一 Nautilin-63 的生物化学。通过制备电泳对 Nautilin-63 进行纯化后,我们证明该可溶性蛋白富含甘氨酸-天冬氨酸,高度糖基化,糖基部分呈酸性,并且能够在体外结合几丁质。有趣的是,Nautilin-63 与体外沉淀的 CaCO3 晶体的形态强烈相互作用,但出乎意料的是,它在体外强烈抑制 CaCO3 沉淀的能力非常弱。通过对其胰蛋白酶肽的从头测序对其部分氨基酸序列进行解析,表明 Nautilin-63 具有短的胶原样结构域。由于针对纯化蛋白产生的特异性多克隆抗体,Nautilin-63 主要在板间珍珠母基质中被免疫定位。总之,Nautilin-63 表现出“混合”生化特性,既有可溶性蛋白,也有不溶性蛋白,这使得它难以按照对珍珠母蛋白的标准观点进行分类。
N63 的蛋白质序列出现在 UniProt 知识库中,登录号为 P86702。