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Biology and receptor interactions ofp97 and the transferrin receptors.

机译:p97和转铁蛋白受体的生物学和受体相互作用。

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摘要

Melanotransferrin, or p97, is an iron binding protein that is expressed as both a glycosylphosphatidylinositol-anchored form and as a soluble form. While the anchored form internalizes iron, the function of the soluble form is still unknown. Soluble p97 levels are increased in the serum and cerebral spinal fluid of Alzheimer disease patients, but the reasons for this increase are undetermined. In order to begin to address the question of function for this soluble protein, possible receptor interactions were studied.; The interaction of p97 and transferrin receptor 1 was characterized with radio-ligand assays and immunofluorescent labeling assays. These experiments demonstrated that p97 interacts with the transferrin receptor 1 in cell binding experiments. However, p97 was not able to deliver iron into the cells via transferrin receptor 1. Furthermore, BIAcore studies were not able to measure any interaction between p97 and transferrin receptor 1.; In the search for other likely candidate receptors of p97, a novel homologue of the transferrin receptor 1 was discovered through mining of the EST database. Expression of this protein was revealed by Northern blot to be largely restricted to the liver. In embryogenesis, the mouse transferrin receptor 2 is present by E15 and continues to increase in expression through E17, in contrast to transferrin receptor 1 that is discernable by E7, increases until E15 and decreases by E17. Transferrin receptor 2 is present on the brain endothelial cells that form the blood-brain barrier implicating it as a candidate receptor for transport of p97 (and iron) into or out of the brain. Interestingly, in transfected cells that over express both transferrin receptor 1 and 2, the receptor is present at the cell surface as a heterodimeric combination of the two receptors.; p97 binds to the mouse transferrin receptor 2, and unlike transferrin receptor 1, also facilitates the uptake of 55Fe through this interaction. Thus, in addition to receptor binding, the functional aspect of this interaction can be demonstrated. Clearly, identification of transferrin receptor 2 as a receptor of p97 is only one of the first important steps toward the ultimate goal of clarifying the function of soluble p97.
机译:黑素转铁蛋白或p97是一种铁结合蛋白,以糖基磷脂酰肌醇固定的形式和可溶的形式表达。虽然锚定形式使铁内在化,但可溶形式的功能仍然未知。阿尔茨海默氏病患者的血清和脑脊髓液中可溶性p97水平升高,但尚不清楚该升高的原因。为了开始解决该可溶性蛋白的功能问题,研究了可能的受体相互作用。 p97和转铁蛋白受体1的相互作用通过放射性配体测定和免疫荧光标记测定进行了表征。这些实验证明在细胞结合实验中p97与运铁蛋白受体1相互作用。然而,p97不能通过转铁蛋白受体1将铁传递到细胞中。此外,BIAcore研究无法测量p97和转铁蛋白受体1之间的任何相互作用。在寻找p97的其他可能候选受体时,通过挖掘EST数据库发现了转铁蛋白受体1的新同源物。该蛋白的表达通过Northern印迹显示出主要限于肝脏。在胚胎发生中,小鼠转铁蛋白受体2由E15存在,并通过E17继续表达增加,与之相反,由E7识别的转铁蛋白受体1一直增加到E15并由E17减少。转铁蛋白受体2存在于形成血脑屏障的脑内皮细胞上,暗示它是p97(和铁)转运进入或转运出大脑的候选受体。有趣的是,在同时表达转铁蛋白受体1和2的转染细胞中,该受体以两种受体的异源二聚体形式存在于细胞表面。 p97与小鼠转铁蛋白受体2结合,与转铁蛋白受体1不同,p97也通过这种相互作用促进 55 Fe的吸收。因此,除了受体结合之外,还可以证明这种相互作用的功能方面。显然,将转铁蛋白受体2鉴定为p97受体只是朝着阐明可溶性p97功能最终目标的第一步。

著录项

  • 作者

    Walker, Brandie Laurel.;

  • 作者单位

    The University of British Columbia (Canada).;

  • 授予单位 The University of British Columbia (Canada).;
  • 学科 Biology Cell.; Biology Molecular.
  • 学位 Ph.D.
  • 年度 2002
  • 页码 162 p.
  • 总页数 162
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 细胞生物学;分子遗传学;
  • 关键词

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