Gotliv Bat-Ami, Kessler Naama, Sumerel Jan L, Morse Daniel E, Tuross Noreen, Addadi Lia, Weiner Steve
Department of Structural Biology, Weizmann Institute of Science, 76100 Rehovot, Israel.
Chembiochem. 2005 Feb;6(2):304-14. doi: 10.1002/cbic.200400221.
Almost all mineralized tissues contain proteins that are unusually acidic. As they are also often intimately associated with the mineral phase, they are thought to fulfill important functions in controlling mineral formation. Relatively little is known about these important proteins, because their acidic nature causes technical difficulties during purification and characterization procedures. Much effort has been made to overcome these problems, particularly in the study of mollusk-shell formation. To date about 16 proteins from mollusk-shell organic matrices have been sequenced, but only two are unusually rich in aspartic and glutamic acids. Here we screened a cDNA library made from the mRNA of the shell-forming cells of a bivalve, Atrina rigida, using probes for short Asp-containing repeat sequences, and identified ten different proteins. Using more specific probes designed from one subgroup of conserved sequences, we obtained the full sequences of a family of seven aspartic acid-rich proteins, which we named "Asprich"; a subfamily of the unusually acidic shell-matrix proteins. Polyclonal antibodies raised against a synthetic peptide of the conserved acidic1 domain of these proteins reacted specifically with the matrix components of the calcitic prismatic layer, but not with those of the aragonitic nacreous layer. Thus the Asprich proteins are constituents of the prismatic layer shell matrix. We can identify different domains within these sequences, including a signal peptide characteristic of proteins destined for extracellular secretion, a conserved domain rich in aspartic acid that contains a sequence very similar to the calcium-binding domain of Calsequestrin, and another domain rich in aspartic acid, that varies between the seven sequences. We also identified a domain with DEAD repeats that may have Mg-binding capabilities. Although we do not know, as yet, the function of these proteins, their generally conserved sequences do indicate that they might well fulfill basic functions in shell formation.
几乎所有矿化组织都含有异常酸性的蛋白质。由于它们通常也与矿质相密切相关,因此被认为在控制矿物质形成方面发挥着重要作用。人们对这些重要蛋白质了解相对较少,因为它们的酸性性质在纯化和表征过程中会带来技术难题。为克服这些问题已付出诸多努力,尤其是在软体动物贝壳形成的研究中。迄今为止,已对来自软体动物贝壳有机基质的约16种蛋白质进行了测序,但只有两种蛋白质富含天冬氨酸和谷氨酸。在此,我们使用针对含天冬氨酸短重复序列的探针,筛选了由双壳类动物坚海笋贝壳形成细胞的mRNA构建的cDNA文库,并鉴定出10种不同的蛋白质。利用从一个保守序列亚组设计的更特异的探针,我们获得了一个由7种富含天冬氨酸的蛋白质组成的家族的完整序列,我们将其命名为“Asprich”;这是异常酸性的贝壳基质蛋白质的一个亚家族。针对这些蛋白质保守酸性1结构域的合成肽产生的多克隆抗体,与方解石棱柱层的基质成分发生特异性反应,但与文石珍珠层的基质成分不发生反应。因此,Asprich蛋白质是棱柱层贝壳基质的组成成分。我们可以在这些序列中识别出不同的结构域,包括注定要分泌到细胞外的蛋白质所特有的信号肽、富含天冬氨酸的保守结构域,该结构域包含一个与肌集钙蛋白钙结合结构域非常相似的序列,以及另一个富含天冬氨酸的结构域,该结构域在这7个序列之间有所不同。我们还鉴定出一个具有DEAD重复序列的结构域,它可能具有结合镁的能力。尽管我们目前还不知道这些蛋白质的功能,但它们普遍保守的序列确实表明它们很可能在贝壳形成中发挥基本功能。