Literature DB >> 15678422

Asprich: A novel aspartic acid-rich protein family from the prismatic shell matrix of the bivalve Atrina rigida.

Bat-Ami Gotliv1, Naama Kessler, Jan L Sumerel, Daniel E Morse, Noreen Tuross, Lia Addadi, Steve Weiner.   

Abstract

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.

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Year:  2005        PMID: 15678422     DOI: 10.1002/cbic.200400221

Source DB:  PubMed          Journal:  Chembiochem        ISSN: 1439-4227            Impact factor:   3.164


  38 in total

1.  Proteomic strategy for identifying mollusc shell proteins using mild chemical degradation and trypsin digestion of insoluble organic shell matrix: a pilot study on Haliotis tuberculata.

Authors:  Laurent Bédouet; Arul Marie; Sophie Berland; Benjamin Marie; Stéphanie Auzoux-Bordenave; Frédéric Marin; Christian Milet
Journal:  Mar Biotechnol (NY)       Date:  2011-12-13       Impact factor: 3.619

2.  Biphasic and dually coordinated expression of the genes encoding major shell matrix proteins in the pearl oyster Pinctada fucata.

Authors:  Takeshi Takeuchi; Kazuyoshi Endo
Journal:  Mar Biotechnol (NY)       Date:  2006-01-01       Impact factor: 3.619

Review 3.  Matrix proteins in the outer shells of molluscs.

Authors:  Cen Zhang; Rongqing Zhang
Journal:  Mar Biotechnol (NY)       Date:  2006-04-18       Impact factor: 3.619

4.  Role of molecular charge and hydrophilicity in regulating the kinetics of crystal growth.

Authors:  S Elhadj; J J De Yoreo; J R Hoyer; P M Dove
Journal:  Proc Natl Acad Sci U S A       Date:  2006-12-07       Impact factor: 11.205

5.  Primary structure of myostracal prism soluble protein (MPSP) in oyster shell, Crassostrea gigas.

Authors:  Seung Woo Lee; Young Moon Kim; Hong Seok Choi; Jai Myung Yang; Cheong Song Choi
Journal:  Protein J       Date:  2006-06       Impact factor: 2.371

6.  Heterogeneity of proteinase inhibitors in the water-soluble organic matrix from the oyster nacre.

Authors:  Laurent Bédouet; Denis Duplat; Arul Marie; Lionel Dubost; Sophie Berland; Marthe Rousseau; Christian Milet; Evelyne Lopez
Journal:  Mar Biotechnol (NY)       Date:  2007-04-03       Impact factor: 3.619

7.  Cloning and characterization of Prisilkin-39, a novel matrix protein serving a dual role in the prismatic layer formation from the oyster Pinctada fucata.

Authors:  Yawei Kong; Gu Jing; Zhenguang Yan; Changzhong Li; Ningping Gong; Fangjie Zhu; Dongxian Li; Yaorun Zhang; Guilan Zheng; Hongzhong Wang; Liping Xie; Rongqing Zhang
Journal:  J Biol Chem       Date:  2009-02-19       Impact factor: 5.157

Review 8.  Biomimetic model systems for investigating the amorphous precursor pathway and its role in biomineralization.

Authors:  Laurie B Gower
Journal:  Chem Rev       Date:  2008-11       Impact factor: 60.622

Review 9.  The role of acidic phosphoproteins in biomineralization.

Authors:  Keith Alvares
Journal:  Connect Tissue Res       Date:  2014 Jan-Feb       Impact factor: 3.417

10.  Carboxylated molecules regulate magnesium content of amorphous calcium carbonates during calcification.

Authors:  Dongbo Wang; Adam F Wallace; James J De Yoreo; Patricia M Dove
Journal:  Proc Natl Acad Sci U S A       Date:  2009-12-02       Impact factor: 11.205

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