Phosphorylated proteins and control over apatite nucleation, crystal growth, and inhibition.
Phosphorylated proteins and control over apatite nucleation, crystal growth, and inhibition.
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DOI:
10.1021/cr0782729
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发表时间:
2008-11
期刊:
影响因子:
62.1
通讯作者:
Veis, Arthur
中科院分区:
文献类型:
--
作者:
George, Anne;Veis, Arthur
Living organisms are capable of inducing the crystallization and deposition of a wide variety of minerals, 1 but the vertebrates mainly utilize the calcium phosphates in constructing their mineral phases in both normal circumstances in bone, dentin, and tooth enamel and in pathological ectopic mineral deposits. The predominant form of the mineral in all situations is as carbonated apatite. However, the extent of mineralization in a particular tissue or organ is quite variable and crystallite size, crystal shape, and packing and organization of the mineral crystals may also be variable. It is clear that the same physical chemical principles must apply to all, but it is equally clear that the organism must tightly regulate the local environment where the mineral is formed. This is an intrinsically complex problem because the mineral crystals of bone and dentin form in the extracellular matrix, external to the cells, which are the ultimate regulators of the process.Years of study of this complex set of problems has led to the general consensus that the cell-controlled processes of mineralization begin with the manufacture of an organic structure within which, or a compartment surface upon which, the mineral crystals may be initiated. The cells secrete and organize macromolecular structures that determine the ultimate character and orientations of the crystals subsequently initiated and grown, but in general, these structures do not themselves have the capacity to initiate mineralization. The incipient crystal nucleation event depends upon the interaction of the structural macromolecules with another set of secreted interactive macromolecules that locate specifically on the structural framework. These interactive molecules are doubly interactive, binding specifically to the framework on
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影响因子:
3.2
作者:
BIANCO, P;RIMINUCCI, M;ROBEY, PG
通讯作者:
ROBEY, PG
影响因子:
4.2
作者:
Campbell, TM;Wong, WT;Mackie, EJ
通讯作者:
Mackie, EJ
DOI:
10.1111/j.1749-6632.1995.tb44615.x
发表时间:
1995-01-01
期刊:
OSTEOPONTIN: ROLE IN CELL SIGNALLING AND ADHESION
影响因子:
--
作者:
BUTLER, WT
通讯作者:
BUTLER, WT
DOI:
10.1111/j.1749-6632.1995.tb44635.x
发表时间:
1995-01-01
期刊:
OSTEOPONTIN: ROLE IN CELL SIGNALLING AND ADHESION
影响因子:
--
作者:
BOSKEY, AL
通讯作者:
BOSKEY, AL
影响因子:
5
作者:
Acebes, C;de la Piedra, C;Herrero-Beaumont, G
通讯作者:
Herrero-Beaumont, G