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大鼠SR-BI胞外域与ApoA-Ⅰ蛋白相互作用的确认
引用本文:李兰松 李维琪 信学雷 曹旭. 大鼠SR-BI胞外域与ApoA-Ⅰ蛋白相互作用的确认[J]. 微生物学通报, 2006, 33(2): 68-73
作者姓名:李兰松 李维琪 信学雷 曹旭
作者单位:[1]中国科学院新疆理化技术研究所,乌鲁木齐830011 [2]中国科学院研究生院,北京100039
基金项目:中国科学院“百人计划”项目资助;2001年“西部之光”项目资助
摘    要:先以含全长SR-BI cDNA序列的重组质粒pMD18-T-rS为摸板进行PCR反应扩增SR-BI得到胞外域cDNA片段,经测序证明正确后,定向克隆到酵母双杂交表达载体,然后与pGBKT7-ApoA-Ⅰ质粒共转化酵母细胞,通过报告基因及酵母交配试验确认了SR-BI的胞外域部分和ApoA-Ⅰ之间的确存,观察到ApoA-Ⅰ与SR-BI胞外域间的相互作用力比与全长的SR-BI问的相互作用力提高了10%。

关 键 词:载脂蛋白AI(ApoA-Ⅰ) B族I型清道夫受体(SR-BI) SR-BI胞外域 基因克隆 酵母双杂交
文章编号:0253-2654(2006)02-0068-06
收稿时间:2005-06-20
修稿时间:2005-08-15

Verification the Interaction of Apolipoprotein AI and the Extracellular Domain of Scavenger Receptors Class B Type I
LI Lan-Song,LI Wei-Qi,XIN Xue-Lei, CAO Xu. Verification the Interaction of Apolipoprotein AI and the Extracellular Domain of Scavenger Receptors Class B Type I[J]. Microbiology China, 2006, 33(2): 68-73
Authors:LI Lan-Song  LI Wei-Qi  XIN Xue-Lei   CAO Xu
Abstract:In this paper,the DNA fragment rSE was amplified by PCR using the recombinant plasmids pMD18-T-rS (containing the hole lines of cDNA of SR-BI) as template. Then the PCR product was directionally cloned into the yeast two hybrid express vector pGADT7 after it was confirmed with sequencing. The recombined vector (named pGADT7-rSE) and pGBKT7-ApoA-I vector was cotransformed in yeast strain AH109. We identified the interaction of ApoA-I and rSE by using report genes and yeast mating. At last,we obsevered that the interaction of ApoA-I and rSE is about 10% more than that of ApoA-I and SR-BI of rat.
Keywords:Apolipoprotein AI(ApoAI)  Scavenger receptor class B type I(SR-BI)  Extracellular domain of SR-BI  Gene clone  Yeast two hybrid
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