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一种屏蔽拓扑结构稳定了胎球蛋白-A与磷酸钙的早期蛋白质-矿物质复合物:时间分辨小角X射线研究。

A shielding topology stabilizes the early stage protein-mineral complexes of fetuin-A and calcium phosphate: a time-resolved small-angle X-ray study.

作者信息

Rochette Christophe N, Rosenfeldt Sabine, Heiss Alexander, Narayanan Theyencheri, Ballauff Matthias, Jahnen-Dechent Willi

机构信息

Physikalische Chemie I, University of Bayreuth, 95444 Bayreuth, Germany.

出版信息

Chembiochem. 2009 Mar 2;10(4):735-40. doi: 10.1002/cbic.200800719.

Abstract

We report on the earliest stages of the formation of complexes of calcium phosphate in the presence of the serum protein alpha(2)-HS glycoprotein/fetuin-A termed calciprotein particles (CPPs). Time-resolved small-angle X-ray scattering (TR-SAXS) and stopped-flow analysis were used to monitor the growth of protein mineral particles nucleating from supersaturated salt solutions. It was found that fetuin-A did not influence the formation of mineral nuclei. However, fetuin-A did prevent the aggregation of nuclei and thus mineral precipitation. Hence, fetuin-A shielded spontaneously formed mineral nuclei, leading to stable calciprotein particles in the first stage of mineralization. Fetuin-A is therefore critically required during the earliest stages of the formation of protein-mineral complexes in order to prevent uncontrolled mineralization.

摘要

我们报告了在血清蛋白α(2)-HS糖蛋白/胎球蛋白-A存在的情况下,磷酸钙复合物形成的最早阶段,这些复合物被称为钙蛋白颗粒(CPPs)。利用时间分辨小角X射线散射(TR-SAXS)和停流分析来监测从过饱和盐溶液中形成的蛋白质矿物质颗粒的生长。结果发现,胎球蛋白-A不影响矿物质核的形成。然而,胎球蛋白-A确实能防止核的聚集,从而防止矿物质沉淀。因此,胎球蛋白-A屏蔽了自发形成的矿物质核,在矿化的第一阶段导致形成稳定的钙蛋白颗粒。因此,在蛋白质-矿物质复合物形成的最早阶段,胎球蛋白-A是至关重要的,以防止不受控制的矿化。

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