Phosphoproteins of the chicken eggshell calcified layer

被引:95
作者
Mann, Karlheinz [1 ]
Olsen, Jesper V. [1 ]
Macek, Boris [1 ]
Gnad, Florian [1 ]
Mann, Matthias [1 ]
机构
[1] Max Planck Inst Biochem, Atb Proteom & Signaltransdukt, Dept Proteom & Signal Transduct, D-82152 Martinsried, Germany
关键词
biomineralization; chicken eggshell; Fourier-transform mass spectrometry; organic matrix; phosphoproteome;
D O I
10.1002/pmic.200600635
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The chicken eggshell matrix is a complex mixture of proteins and proteoglycans. It also contains phosphoproteins that are thought to affect mineralization of the matrix. Several of the matrix phosphoproteins, such as the major component osteopontin, have already been identified as phosphoproteins in other tissues, but the phosphorylation status of the eggshell matrix forms was unknown. The phosphopeptides, obtained after cleavage of the matrix proteins with several different cleavage methods, were enriched by anion-exchange chromatography and reversible binding to titanium oxide and identified by LC-MSn or pseudo-MSn analysis following neutral loss scanning. Altogether we identified 39 phosphorylated matrix proteins, 22 of which were not known to be phosphorylated before. Eight of the proteins were identified as eggshell matrix components for the first time. Together these proteins contained more than 150 different phosphorylation sites, 103 of which were determined with high confidence. Among the major phosphorylated proteins of the chicken eggshell matrix were osteopontin and the eggshell-specific proteins ovocleidin-17, ovocleidin-116, and ovocalyxin-32.
引用
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页码:106 / 115
页数:10
相关论文
共 62 条
[51]  
SINGH K, 1990, J BIOL CHEM, V265, P18696
[52]   Osteopontin [J].
Sodek, J ;
Ganss, B ;
McKee, MD .
CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE, 2000, 11 (03) :279-303
[53]   Nucleobindin -: a Ca2+-binding protein present in the cells and mineralized tissues of the tooth [J].
Somogyi, E ;
Petersson, U ;
Sugars, RV ;
Hultenby, K ;
Wendell, M .
CALCIFIED TISSUE INTERNATIONAL, 2004, 74 (04) :366-376
[54]   In situ phosphorylation of bone and dentin proteins by the casein kinase II-like enzyme [J].
Suzuki, Y ;
Yamaguchi, A ;
Ikeda, T ;
Kawase, T ;
Saito, S ;
Mikuni-Takagaki, Y .
JOURNAL OF DENTAL RESEARCH, 1998, 77 (10) :1799-1806
[55]   FIBRONECTIN FROM CHICKEN-EMBRYO FIBROBLASTS CONTAINS COVALENTLY BOUND PHOSPHATE [J].
TENG, MH ;
RIFKIN, DB .
JOURNAL OF CELL BIOLOGY, 1979, 80 (03) :784-791
[56]   Analysis of a sub-proteome which co-purifies with and is phosphorylated by the Golgi casein kinase [J].
Tibaldi, E ;
Arrigoni, G ;
Brunati, AM ;
James, P ;
Pinna, LA .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2006, 63 (03) :378-389
[57]   Phosphorylation of the proteins of the extracellular matrix of mineralized tissues by casein kinase-like activity [J].
Veis, A ;
Sfeir, C ;
Wu, CB .
CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE, 1997, 8 (04) :360-379
[58]   POSTTRANSLATIONAL PROCESSING OF CHROMOGRANIN-A - DIFFERENTIAL DISTRIBUTION OF PHOSPHORYLATED VARIANTS OF PANCREASTATIN AND FRAGMENTS 248-313 AND 297-313 IN BOVINE PANCREAS AND ILEUM [J].
WATKINSON, A ;
ROGERS, M ;
DOCKRAY, GJ .
BIOCHEMICAL JOURNAL, 1993, 295 :649-654
[59]  
WELCH WJ, 1983, J BIOL CHEM, V258, P7102
[60]  
Wieland WH, 2004, BIOCHEM J, V380, P669, DOI [10.1042/BJ20040200, 10.1042/bj20040200]