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Updated: Jun 25, 2026

Hybrid µCT-FMT imaging and image analysis
Published on: June 4, 2015
A shielding topology stabilizes the early stage protein-mineral complexes of fetuin-A and calcium phosphate: a
Christophe N Rochette1, Sabine Rosenfeldt, Alexander Heiss
1Physikalische Chemie I, University of Bayreuth, 95444 Bayreuth, Germany.
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.

