ACTIVE SITES OF GLYCYL-TRNA SYNTHETASE--EXTRACELLULAR SEA URCHIN EMBRYO PROTEINS

甘氨酰-TRNA合成酶活性位点--海胆胚胎胞外蛋白

基本信息

项目摘要

Students will work in two broad research areas. In the first project, structure and functions of the enzyme glycyl-tRNA synthetase will be investigated in order to provide information concerning basic molecular mechanisms of protein synthesis. This work will concentrate particularly on the role placed by dissimilar subunits in the recognition and activation of tRNA and ATP. Affinity labeling reagents will be employed to probe the enzyme's recognition sites and modified peptides isolated to locate essential amino acid residues in the active site of the enzyme. Subsequent studies will be directed at a closely related enzyme, phenylalanyl-tRNA synthetase. Computer analysis will compare amino acid sequences so identified with those of other aminoacyl -tRNA synthetases to better understand how these enzymes as a group accomplish their essential role in vivo. In the second project, the proteins forming the extracellular matrix of sea urchin embryos following fertilization will be investigated. By purifying the protein components of the hyaline layer and the fertilization envelope, we hope to provide an understanding of the molecular mechanisms of cellular organization in the embryo and the manner in which the block to polyspermic fertilization is accomplished. A major goal of this work is to provide information regarding the amino acid sequence of three proteins already isolated by students in the laboratory. This work aims to correlate amino acid sequences of the proteins with DNA sequences of hyalin-associated proteins presently being completed in other laboratories. Together, these data can serve to understand how the three proteins are related to one another and to other calcium-binding and extracellular matrix protein as well as how these proteins are regulated developmentally and how they perform their essential biological role. The primary goal of this project is to provide a scientific environment which gives these students the opportunity to succeed as young scientists and an atmosphere which supports and encourages academic involvement and achievement. Students form our laboratory have established a strong record of accomplishment. Of the fifty-nine students who have completed projects since 1980, 44% have entered graduate or professional programs.
学生将在两个广泛的研究领域工作。 在第一个项目中, 甘氨酰-tRNA合成酶的结构和功能 进行调查,以提供有关基本分子的信息 蛋白质合成的机制。 这项工作将特别集中 关于不同亚基在识别和识别中的作用 tRNA 和 ATP 的激活。 将使用亲和标记试剂 探测酶的识别位点和分离的修饰肽 找到酶活性位点的必需氨基酸残基。 后续研究将针对密切相关的酶, 苯丙氨酰-tRNA 合成酶。计算机分析将比较氨基酸 与其他氨酰基-tRNA合成酶的序列如此鉴定以 更好地了解这些酶作为一个整体如何实现其基本功能 体内的作用。 在第二个项目中,形成细胞外基质的蛋白质 将研究受精后的海胆胚胎。 经过 纯化透明层的蛋白质成分和 受精信封,我们希望提供一个了解 胚胎细胞组织的分子机制和方式 其中多精受精的阻断得以完成。 一个专业 这项工作的目标是提供有关氨基酸的信息 学生已在实验室分离出三种蛋白质的序列。 这项工作旨在将蛋白质的氨基酸序列与 DNA 关联起来 透明蛋白相关蛋白的序列目前正在其他领域完成 实验室。 这些数据共同可以帮助我们了解这三者如何 蛋白质彼此相关并与其他钙结合和 细胞外基质蛋白以及这些蛋白的调节方式 发育以及它们如何发挥其重要的生物学作用。 这 该项目的主要目标是提供一个科学环境 为这些学生提供作为年轻科学家取得成功的机会 支持和鼓励学术参与的氛围 成就。 我们实验室的学生已经建立了强大的 成就记录。 在已完成学业的五十九名学生中 自 1980 年以来的项目中,44% 已进入研究生或专业课程。

项目成果

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GLENN M NAGEL其他文献

GLENN M NAGEL的其他文献

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{{ truncateString('GLENN M NAGEL', 18)}}的其他基金

ACTIVE SITES OF GLYCYL-TRNA SYNTHETASE--EXTRACELLULAR SEA URCHIN EMBRYO PROTEINS
甘氨酰-TRNA合成酶活性位点--海胆胚胎胞外蛋白
  • 批准号:
    6240369
  • 财政年份:
    1997
  • 资助金额:
    --
  • 项目类别:
SMALL INSTRUMENTATION GRANT
小型仪器补助金
  • 批准号:
    3524995
  • 财政年份:
    1993
  • 资助金额:
    --
  • 项目类别:
DOMAIN LABELING OF FIBRINOGEN & GLYCYL-TRNA SYNTHETASE
纤维蛋白原的结构域标记
  • 批准号:
    3057003
  • 财政年份:
    1990
  • 资助金额:
    --
  • 项目类别:
SUBUNIT FUNCTION AND TOPOLOGY IN GLYCYL-TRNA SYNTHETASE
甘氨酰-TRNA 合成酶中的亚基功能和拓扑结构
  • 批准号:
    3438440
  • 财政年份:
    1985
  • 资助金额:
    --
  • 项目类别:
ACTIVE SITES OF GLYCYL-TRNA SYNTHETASE--EXTRACELLULAR SEA URCHIN EMBRYO PROTEINS
甘氨酰-TRNA合成酶活性位点--海胆胚胎胞外蛋白
  • 批准号:
    5212019
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
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