Cell Cycle proteomicsin Xenopus

爪蟾细胞周期蛋白质组学

• 批准号: 8876721
• 负责人: MARC Wallace KIRSCHNER
• 金额: $ 49.68万
• 依托单位: HARVARD MEDICAL SCHOOL
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-08-15 至 2017-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8876721
• 关键词: Affect; Algorithms; Biochemical; Biochemistry; Bioinformatics; Biology; Cell Cycle; Cell Cycle Regulation; Cell Nucleus; Cell physiology; Cells; Characteristics; Communities; Complex; Cytoplasm; Cytoskeleton; Data; Databases; Development; Dose; Drug Design; Drug Targeting; Embryo; Embryonic Development; Event; Experimental Designs; Fertilization; Genetic Transcription; Health; Human; Image; Inflammation; Investigation; Knowledge; Label; Learning; Life; Malignant Neoplasms; Mass Spectrum Analysis; Measures; Meiosis; Methods; Methylation; Microtubules; Modification; Oocytes; Pathway interactions; Peptides; Pharmaceutical Preparations; Phosphorylation Site; Post-Translational Protein Processing; Preparation; Protein Dynamics; Proteins; Proteolysis; Proteome; Proteomics; Qualifying; Reaction; Reaction Time; Reading; Regulation; Relative (related person); Research; Resolution; Role; Sampling; Site; System; Techniques; Technology; Time; Titrations; Translations; Ubiquitination; Xenopus; Xenopus Proteins; Yeasts; base; blastomere structure; data mining; deep sequencing; egg; gastrulation; genetic regulatory protein; improved; inhibitor/antagonist; interest; protein complex; research study; small molecule; tandem mass spectrometry; tool; wiki; zygote

DESCRIPTION (provided by applicant): Proteomics has special significance for Xenopus research because key events in meiosis, fertilization and early development are regulated at the level of translation, post- translational modification and proteolysis, and not by transcription. Proteomics is the only tool for systematically investigating these levels of regulation and discovering new mechanisms. We propose to develop a cutting edge proteomic research platform for Xenopus embryos and egg extract by migrating technology developed in human and yeast systems, and to publicly disseminate the databases and tools we develop. We will also optimize methods for proteomic analysis of protein complexes and compartments in egg extract. Using these tools we will quantify relative amounts of >5,000 proteins, >10,000 phosphorylation sites and >1,500 ubiquitination sites in early development and in egg extracts under normal and perturbed conditions. We will investigate the mechanism of cell cycle regulation, how the cell cycle changes during early development, how microtubules are nucleated, and how embryos detect changes in the nucleus to cytoplasm ratio.

描述（由申请人提供）：