国家自然科学基金(30200103)和湖南省教育厅青年基金(02B039)资助项目.
This work was supported by grants from The National Natural Sciences Foundation of China (30200103) and Hunan Province Educational Office Young Foundation(02B039).
突触相关蛋白家族成员的功能与神经突触膜上的谷氨酸酯受体和钾离子通道的定位和功能有关,参与神经递质的释放、神经的生长、发育及修复.为分析一个新的人突触相关蛋白基因(FRG4)的抗原表位和该蛋白质在血管细胞的表达,从人胎肝文库PCR扩增获得FRG4基因全长cDNA序列.通过生物信息学分析,预测FRG4编码氨基酸序列的二级结构、抗原决定簇和功能结构域;选取抗原13肽PKLVKEEVFWRNY,采用固相多肽合成法合成了FRG4抗原多肽,免疫新西兰白兔获得兔抗人FRG4多抗;免疫组化检测该蛋白质在人血管细胞中的表达.高效液相色谱检测显示制备的兔抗人FRG4多克隆抗体纯度达82.79%,抗体滴度为1∶16 000,蛋白质印迹证实该抗体具有较好的反应性和特异性,免疫组化证实,其主要在平滑肌细胞和内皮细胞的胞浆中表达.结果表明,成功制备了兔抗人FRG4抗体,FRG4蛋白主要在细胞胞浆中表达,与生物信息学分析结果一致.
A family of synapse-associated protein(SAPs) has recently emerged as a central player in the molecular organization of synapses. This work is to analyze the epitope of a novel Homo sapiens synapse associated-protein(FRG4) and synthesize polyclonal antibody, then research FRG4 protein expression in smooth muscle cells and endothelial cells. FRG4 full-length sequence was obtained by PCR from human fetal liver library. Its epitope, motifs and the second structure of amino acids encoded were detected by bioinformatics technique. By solid-phase peptide synthesis method to synthesize FRG4 peptides, then peptides were immunized to rabbits; by immunohistochemistry to detect the expression of FRG4 in vascular smooth muscle cells and endothelial cells. The 13-peptides PKLVKEEVFWRNY was selected by bioinformatic analysis to synthesize rabbit anti-human FRG4 polyclonal antibody. Antibody purity was 82.79% and antibody dilution was 1∶16 000 detected by ELISA. The antibody has a good reaction and speciality in Western blot, it was mainly expressed in the cytoplasm of smooth muscle cells and endothelial cells by immunohistochemistry. The results suggested a novel Homo sapiens synapse associated protein (FRG4) antibody was synthesized successfully. FRG4 expressed mainly in the cytoplasm of vascular smooth muscle cells and endothelial cells.
杨向东,王仁,刘俊文,屈顺林,郭芳,王蕾,盛树力.人突触相关蛋白抗原表位分析、抗体制备及表达研究[J].生物化学与生物物理进展,2004,31(12):1119-1124
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