Modulation of Calcium Oxalate Dihydrate Growth by Selective Crystal-face Binding of Phosphorylated Osteopontin and Polyaspartate Peptide Showing Occlusion by Sectoral (Compositional) Zoning *
Journal of Biological Chemistry, ISSN: 0021-9258, Vol: 284, Issue: 35, Page: 23491-23501
2009
- 66Citations
- 47Captures
- 2Mentions
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Metrics Details
- Citations66
- Citation Indexes66
- 66
- CrossRef46
- Captures47
- Readers47
- 47
- Mentions2
- References2
- Wikipedia2
Article Description
Calcium oxalate dihydrate (COD) mineral and the urinary protein osteopontin/uropontin (OPN) are commonly found in kidney stones. To investigate the effects of OPN on COD growth, COD crystals were grown with phosphorylated OPN or a polyaspartic acid-rich peptide of OPN (DDLDDDDD, poly-Asp 86–93 ). Crystals grown with OPN showed increased dimensions of the {110} prismatic faces attributable to selective inhibition at this crystallographic face. At high concentrations of OPN, elongated crystals with dominant {110} faces were produced, often with intergrown, interpenetrating twin crystals. Poly-Asp 86–93 dose-dependently elongated crystal morphology along the {110} faces in a manner similar to OPN. In crystal growth studies using fluorescently tagged poly-Asp 86–93 followed by imaging of crystal interiors using confocal microscopy, sectoral (compositional) zoning in COD was observed resulting from selective binding and incorporation (occlusion) of peptide exclusively into {110} crystal sectors. Computational modeling of poly-Asp 86–93 adsorption to COD {110} and {101} surfaces also suggests increased stabilization of the COD {110} surface and negligible change to the natively stable {101} surface. Ultrastructural, colloidal-gold immunolocalization of OPN by transmission electron microscopy in human stones confirmed an intracrystalline distribution of OPN. In summary, OPN and its poly-Asp 86–93 sequence similarly affect COD mineral growth; the {110} crystallographic faces become enhanced and dominant attributable to {110} face inhibition by the protein/peptide, and peptides can incorporate into the mineral phase. We, thus, conclude that the poly-Asp 86–93 domain is central to the OPN ability to interact with the {110} faces of COD, where it binds to inhibit crystal growth with subsequent intracrystalline incorporation (occlusion).
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0021925818607781; http://dx.doi.org/10.1074/jbc.m109.021899; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=69949178239&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/19581305; https://linkinghub.elsevier.com/retrieve/pii/S0021925818607781; http://www.jbc.org/lookup/doi/10.1074/jbc.M109.021899; https://syndication.highwire.org/content/doi/10.1074/jbc.M109.021899; https://dx.doi.org/10.1074/jbc.m109.021899
Elsevier BV
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