淡江大學機構典藏:Item 987654321/46931
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    Please use this identifier to cite or link to this item: http://tkuir.lib.tku.edu.tw:8080/dspace/handle/987654321/46931


    Title: 新穎啤酒酵母菌蛋白質甲基轉移脢YJR129Cp之探討
    Other Titles: Investigation of a Novel Protein Methyltransferase YJR129Cp from Saccharomyces cerevisiae
    Authors: 陳銘凱
    Contributors: 淡江大學生命科學研究所
    Keywords: 甲基化;蛋白質甲基轉移酶;啤酒酵母菌;蛋白質體學;methylation;protein methyltransferase;Saccharomyces cerevisiae;proteomics
    Date: 2008
    Issue Date: 2010-04-15 15:37:15 (UTC+8)
    Abstract: 本計劃是以本實驗室先前的發現為基礎。此發現已於C012-1中描述,證實了啤酒酵母菌之YJR129Cp為一真實具有活性之新穎蛋白質甲基轉移酶。此新發現利用一維電泳分析顯示,其蛋白質受質之分子量為95 kDa, 72 kDa, 55 kDa, 43 kDa,pI值為 6~7。本計劃將進一步利用蛋白質體學方法找出YJR129Cp之蛋白質受質;即進一步利用二維電泳分離及質譜分析來鑑定出蛋白質受質種類。並將利用定點突變、基因剔除、及甲基化反應等方式來證明是否YJR129Cp於體外及體內皆具有專一的活性。最後,計劃將延伸至功能方面的探討,此部分將借助於雙雜合篩選及合成致死基因篩選等技術。 This proposal is based on the previous finding in our lab that YJR129Cp of Saccharomyces cerevisiae is a bona fide, novel protein methyltransferase, as presented in C012-1. This new discovery indicates that the protein substrate has a molecular weight of 95 kDa, 72 kDa, 55 kDa, 43 kDa, and pI 6~7 in one-dimensional electrophoretic analysis. Here, identification of the protein substrate is planned by the proteomics approach; that is, two-dimensional electrophoretic separation followed by mass spectrometry. The specificity of both in vitro and in vivo activity of YJR129Cp is also planned to be verified using site-directed mutagenesis, gene deletion, and both in vitro and in vivo methylation assay. Finally, the study will be extended to the functional aspect by two-hybrid screening and synthetic lethal screening.
    Appears in Collections:[Graduate Institue of Life Sciences] Research Paper

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