Influence of Selected Artificial Peptides on Calcium Carbonate Precipitation - A Quantitative Study

被引:61
作者
Gebauer, Denis [1 ]
Verch, Andreas [1 ]
Boerner, Hans G. [1 ]
Coelfen, Helmut [1 ]
机构
[1] Max Planck Inst Colloids & Interfaces, D-14476 Potsdam, Germany
关键词
PROTEIN SECONDARY STRUCTURE; CIRCULAR-DICHROISM SPECTRA; CRYSTAL-GROWTH; MATRIX PROTEIN; STRUCTURAL-CHARACTERIZATION; SHELL PROTEINS; NACRE PROTEIN; IN-VITRO; BIOMINERALIZATION; CRYSTALLIZATION;
D O I
10.1021/cg801292p
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Calcium carbonate is an abundant biomineral with fascinating shapes and properties. Much effort is spent to study how creatures can control mineral formation. We present a quantitative study of the early stage of calcium carbonate precipitation in the presence of artificial peptide additives, the sequences of which were derived in phage assays to have aragonite binding affinity. A novel crystallization assay shows that the peptide additives inhibit nucleation of calcite. Analysis of the precipitated particles and comparison with nucleation inhibition confirm our recent findings, which suggest that calcitic and vateritic short-range order is already preformed in stable prenucleation clusters, which form amorphous intermediates after nucleation reflecting similar structures and finally become crystalline. In the long run, this process facilitates the control of polymorph formation by the design of the binding affinity of additives to different polymorphs (i.e., the polymorph bound weakest by the additive is to be formed as its formation is least inhibited). These findings facilitate a novel understanding of mineralization control and provide a basis for the analysis of biological peptide sequences and for the analysis of their role in biomineralization processes.
引用
收藏
页码:2398 / 2403
页数:6
相关论文
共 50 条
[1]   Taking advantage of disorder: Amorphous calcium carbonate and its roles in biomineralization [J].
Addadi, L ;
Raz, S ;
Weiner, S .
ADVANCED MATERIALS, 2003, 15 (12) :959-970
[2]   Rapid, room-temperature formation of crystalline calcium molybdate phosphor microparticles via peptide-induced precipitation [J].
Ahmad, Gul ;
Dickerson, Matthew B. ;
Church, Benjamin C. ;
Cai, Ye ;
Jones, Sharon E. ;
Naik, Rajesh R. ;
King, Jeffrey S. ;
Summers, Christopher J. ;
Kroger, Nils ;
Sandhage, Kenneth H. .
ADVANCED MATERIALS, 2006, 18 (13) :1759-+
[3]  
[Anonymous], 1989, On Biomineralization
[4]   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
[5]  
BELCHER AM, 2000, BIOMINERALISATION, P247
[6]   The nacre protein perlucin nucleates growth of calcium carbonate crystals [J].
Blank, S ;
Arnoldi, M ;
Khoshnavaz, S ;
Treccani, L ;
Kuntz, M ;
Mann, K ;
Grathwohl, G ;
Fritz, M .
JOURNAL OF MICROSCOPY-OXFORD, 2003, 212 :280-291
[7]   ADVANTAGEOUS APPLICATIONS OF AZABENZOTRIAZOLE (TRIAZOLOPYRIDINE)-BASED COUPLING REAGENTS TO SOLID-PHASE PEPTIDE-SYNTHESIS [J].
CARPINO, LA ;
EL-FAHAM, A ;
MINOR, CA ;
ALBERICIO, F .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1994, (02) :201-203
[8]  
Chan WC, 2000, PRACT APPROACH SER, V222, P41
[9]   Identification of an "acidic" C-terminal mineral modification sequence from the mollusk shell protein Asprich [J].
Collino, S ;
Kim, IW ;
Evans, JS .
CRYSTAL GROWTH & DESIGN, 2006, 6 (04) :839-842
[10]   Identification and structural characterization of an unusual RING-like sequence within an extracellular biomineralization protein, AP7 [J].
Collino, Sebastiano ;
Kim, Il Won ;
Evans, John Spencer .
BIOCHEMISTRY, 2008, 47 (12) :3745-3755