课题基金 / 基金详情

PROTEIN INHIBITORS OF CALCIUM PHOSPHATE PRECIPITATION

PROTEIN INHIBITORS OF CALCIUM PHOSPHATE PRECIPITATION
磷酸钙沉淀的蛋白质抑制剂
批准号:
3219891
负责人:
DAVID H SCHLESINGER
金额:
$14.68万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1982
资助国家:
美国
项目状态:
已结题
起止时间:
1982-02-01 至 1990-01-31

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中文摘要
翻译
人类唾液的钙含量是过饱和的
英文摘要
Human saliva is supersaturated with respect to the calcium phosphate salts which form dental enamel, a condition which would normally generate unwanted and potentially harmful precipitation of calcium phosphate salts in the salivary glands and on the teeth. These, undesirable side effects are prevented by 2 salivary phosphoprotein, statherin and the acidic proline-rich proteins (PRP), which are potent inhibitors of calcium phosphate precipitation. Because of their activities, saliva provides a prospective, reparative but stable environment which is important for maintaining the health of the teeth. Our objectives are to gain a sound understanding of these protective and reparative functions, to relate them to oral health and disease, and to achieve a level of knowledge which will help to ensure that these natural oral defense mechanisms fully express themselves in the mouth. Previous studies by the applicant and co-investigators led to the identification of statherin and the PRP's as inhibitors of calcium phosphate precipitation, made a major contribution to the determination of their structures, and made substantial advances towards establishing the molecular mechanisms by which these unusual macromolecule act. It is now proposed to advance understanding of these functions and mechanisms of action of these molecules in the following ways: 1) by synthesizing phosphoserine- containing peptide analogs of statherin and the PRP's for structure studies b) by investigating mechanisms of post-translational phosphorylation of statherin and the PRP's by using serine- containing peptide analogs specifically synthesized for this purpose, 3) by studying analogs of statherin and the PRP's from nonhuman mammals to gain further insights into structure-function relationships and evolutionary aspects of these molecules, and 4) by studying specific aspects of the behavior and fate of statherin and the PRP's in the oral cavity, an important site at which they act but where they are subject to degradation by oral microflora. The work will be advanced by use of modern gas-phase microsequencing methods and solid phase peptide synthesis techniques. From this work will come advances in understanding of an important tooth-protective system and new knowledge of the modulation of the chemistry of calcium phosphates by specific and unusual phosphoprotein.
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STRUCTURAL STUDIES ON THE PLASMODIUM SURFACE PROTEINS
  • 批准号:
    3133555
  • 项目类别:
  • 资助金额:
    $13.58万
  • 财政年份:
    1985
  • 负责人:
    DAVID H SCHLESINGER
  • 依托单位:
STRUCTURAL STUDIES ON THE PLASMODIUM SURFACE PROTEINS
  • 批准号:
    3133554
  • 项目类别:
  • 资助金额:
    $13.57万
  • 财政年份:
    1985
  • 负责人:
    DAVID H SCHLESINGER
  • 依托单位:
STRUCTURAL STUDIES ON THE PLASMODIUM SURFACE PROTEINS
  • 批准号:
    3133551
  • 项目类别:
  • 资助金额:
    $14.73万
  • 财政年份:
    1985
  • 负责人:
    DAVID H SCHLESINGER
  • 依托单位:
PROTEIN INHIBITORS OF CALCIUM PHOSPHATE PRECIPITATION
  • 批准号:
    3219889
  • 项目类别:
  • 资助金额:
    $15.01万
  • 财政年份:
    1982
  • 负责人:
    DAVID H SCHLESINGER
  • 依托单位:
海外基金