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Proteomic evaluation of biological nanoparticles isolated from human kidney stones and calcified arteries

Acta Biomater. 2010 Oct; 6(10)
Shiekh, F.A.Charlesworth, J.E.Kim, S.-H.Hunter, L.W.Jayachandran, M.Miller, V.M.Lieske, J.C. Department of Internal Medicine
Department of Laboratory Medicine and Pathology
Department of Physiology and Biomedical Engineering
Department of Surgery
Department of Electron Microscopy Core Facility
Mayo Clinic Rochester, MN, USA
2010 Biology

Calcifying biological nanoparticles (NPs) develop under cell culture conditions from homogenates of diverse tissue samples displaying extraosseous mineralization, including kidney stones and calcified aneurysms. Probes to definitively identify NPs in biological systems are lacking. Therefore, the aim of this study was to begin to establish a proteomic biosignature of NPs in order to facilitate more definitive investigation of their contribution to disease. Biological NPs derived from human kidney stones and calcified aneurysms were completely decalcified by overnight treatment with ethylenediaminetetraacetic acid or brief incubation in HCl, as evidenced by lack of a calcium shell and of Alizarin Red S staining, by transmission electron microscopy and confocal microscopy, respectively.

Decalcified NPs contained numerous proteins, including some from bovine serum and others of prokaryotic origin. Most prominent of the latter group was EF-Tu, which appeared to be identical to EF-Tu from Staphylococcus epidermidis. A monoclonal antibody against human EF-Tu recognized a protein in Western blots of total NP lysate, as well as in intact NPs by immunofluorescence and immunogold EM.

Approximately 8% of NPs were quantitatively recognized by the antibody using flow cytometry. Therefore, we have defined methods to reproducibly decalcify biological NPs, and identified key components of their proteome. These elements, including EF-Tu, can be used as biomarkers to further define the processes that mediate propagation of biological NPs and their contribution to disease.

The article was published in: Acta Biomater. 2010 Oct; 6(10): 4065–4072.

Full article

This work was supported (in part) by the Fetzer Franklin Fund of the John E. Fetzer Memorial Trust.