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

被引:205
作者
Gotliv, BA
Kessler, N
Sumerel, JL
Morse, DE
Tuross, N
Addadi, L
Weiner, S [1 ]
机构
[1] Weizmann Inst Sci, Dept Biol Struct, IL-76100 Rehovot, Israel
[2] Univ Calif Santa Barbara, Inst Collaborat Biotechnol, Santa Barbara, CA 93106 USA
[3] Univ Calif Santa Barbara, Dept Mol Cellular & Dev Biol, Santa Barbara, CA 93106 USA
[4] Harvard Univ, Dept Anthropol, Cambridge, MA 02138 USA
关键词
aspartic acid; biomineralization; calcite; mollusk shell; organic matrix; proteins;
D O I
10.1002/cbic.200400221
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 shelf-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. Polyclonol antibodies raised against a synthetic peptide of the conserved acidic 1 domain of these proteins reacted specifically with the matrix components of the calcitic prismatic layer, but not with those of the aragonitic nacreous foyer, Thus the Asprich proteins are constituents of the prismatic layer shell matrix. We con 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.
引用
收藏
页码:304 / 314
页数:11
相关论文
共 61 条
[1]   CONTROL AND DESIGN PRINCIPLES IN BIOLOGICAL MINERALIZATION [J].
ADDADI, L ;
WEINER, S .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1992, 31 (02) :153-169
[2]   GROWTH AND DISSOLUTION OF ORGANIC-CRYSTALS WITH TAILOR-MADE INHIBITORS - IMPLICATIONS IN STEREOCHEMISTRY AND MATERIALS SCIENCE [J].
ADDADI, L ;
BERKOVITCHYELLIN, Z ;
WEISSBUCH, I ;
VANMIL, J ;
SHIMON, LJW ;
LAHAV, M ;
LEISEROWITZ, L .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1985, 24 (06) :466-485
[3]   A CHEMICAL-MODEL FOR THE COOPERATION OF SULFATES AND CARBOXYLATES IN CALCITE CRYSTAL NUCLEATION - RELEVANCE TO BIOMINERALIZATION [J].
ADDADI, L ;
MORADIAN, J ;
SHAY, E ;
MAROUDAS, NG ;
WEINER, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (09) :2732-2736
[4]  
Addadi L., 1991, P29
[5]  
Addadi L., 1989, STEREOCHEMICAL STRUC, P133
[6]  
ADDADI L, 1985, ANGEW CHEM, V97, P476
[7]   INTERACTIONS OF VARIOUS SKELETAL INTRACRYSTALLINE COMPONENTS WITH CALCITE CRYSTALS [J].
ALBECK, S ;
AIZENBERG, J ;
ADDADI, L ;
WEINER, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (25) :11691-11697
[8]   Control of crystal phase switching and orientation by soluble mollusc-shell proteins [J].
Belcher, AM ;
Wu, XH ;
Christensen, RJ ;
Hansma, PK ;
Stucky, GD ;
Morse, DE .
NATURE, 1996, 381 (6577) :56-58
[9]   BIOLOGICAL-CONTROL OF CRYSTAL TEXTURE - A WIDESPREAD STRATEGY FOR ADAPTING CRYSTAL PROPERTIES TO FUNCTION [J].
BERMAN, A ;
HANSON, J ;
LEISEROWITZ, L ;
KOETZLE, TF ;
WEINER, S ;
ADDADI, L .
SCIENCE, 1993, 259 (5096) :776-779
[10]   INTERACTIONS OF SEA-URCHIN SKELETON MACROMOLECULES WITH GROWING CALCITE CRYSTALS - A STUDY OF INTRACRYSTALLINE PROTEINS [J].
BERMAN, A ;
ADDADI, L ;
WEINER, S .
NATURE, 1988, 331 (6156) :546-548