首页> 美国卫生研究院文献>The Journal of Biological Chemistry >Modulation of Calcium Oxalate Dihydrate Growth by Selective Crystal-face Binding of Phosphorylated Osteopontin and Polyaspartate Peptide Showing Occlusion by Sectoral (Compositional) Zoning
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Modulation of Calcium Oxalate Dihydrate Growth by Selective Crystal-face Binding of Phosphorylated Osteopontin and Polyaspartate Peptide Showing Occlusion by Sectoral (Compositional) Zoning

机译:磷酸化骨桥蛋白和聚天冬氨酸肽的选择性晶面结合对草酸钙二水合物生长的调节显示其被部门(成分)区分开。

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摘要

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-Asp86–93). 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-Asp86–93 dose-dependently elongated crystal morphology along the {110} faces in a manner similar to OPN. In crystal growth studies using fluorescently tagged poly-Asp86–93 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-Asp86–93 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-Asp86–93 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-Asp86–93 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).
机译:二水草酸钙(COD)矿物质和尿蛋白骨桥蛋白/尿桥蛋白(OPN)通常在肾结石中发现。为了研究OPN对COD生长的影响,将COD晶体与磷酸化OPN或富含OPN的聚天冬氨酸的肽(DDLDDDDD,poly-Asp 86-93 )一起生长。用OPN生长的晶体显示出{110}棱柱形面的尺寸增加,这归因于在该结晶面的选择性抑制。在高浓度的OPN时,会产生具有{110}主面的细长晶体,通常带有互生,互穿的双晶。 Poly-Asp 86-93 沿{110}面的剂量依赖性拉长的晶体形态,类似于OPN。在使用荧光标记的poly-Asp 86-93 进行晶体生长研究,然后使用共聚焦显微镜对晶体内部成像的过程中,观察到了COD中的扇形(组成)分区,这是由于肽的选择性结合和掺入(闭塞)导致的仅进入{110}晶体扇区。聚Asp 86-93 对COD {110}和{101}表面的吸附的计算模型还表明,COD {110}表面的稳定性增强,而对本征稳定的{101}表面的变化可忽略不计。透射电子显微镜在人结石中对OPN的超微结构,胶体金免疫定位证实了OPN的晶内分布。总之,OPN及其poly-Asp 86-93 序列对COD矿物质的生长有相似的影响。 {110}晶体学面变得增强,并主要归因于蛋白质/肽对{110}面的抑制,并且肽可以掺入矿物相。因此,我们得出的结论是,poly-Asp 86-93 域对于OPN与COD的{110}面相互作用的能力至关重要,在OPN中,其结合抑制晶体生长并随后进行晶体内掺入(咬合)。

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