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Z-VRPR-FMK对Burkitt淋巴瘤细胞内MALT1和A20蛋白表达的影响
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作者 王佳蕊 冯江龙 杨文秀 《贵州医科大学学报》 CAS 2017年第10期1125-1129,共5页
目的:用聚丙烯酸甲酯/离子霉素(PMA/IONO)和MALT1抑制剂Z-VRPR-FMK刺激Burkitt淋巴瘤细胞,检测细胞内MALT1和A20蛋白的表达。方法:采用200μg/L+1μmol/L的PMA/IONO和不同浓度(25、50和75μmol/L)的Z-VRPR-FMK、在不同的作用时间(0.25、... 目的:用聚丙烯酸甲酯/离子霉素(PMA/IONO)和MALT1抑制剂Z-VRPR-FMK刺激Burkitt淋巴瘤细胞,检测细胞内MALT1和A20蛋白的表达。方法:采用200μg/L+1μmol/L的PMA/IONO和不同浓度(25、50和75μmol/L)的Z-VRPR-FMK、在不同的作用时间(0.25、0.5和2 h)下刺激培养的Burkitt淋巴瘤细胞Raji,根据各组细胞中A20蛋白的表达情况确定抑制剂Z-VRPR-FMK的最佳作用浓度及时间;将培养的Raji细胞分为设对照组、激动剂PMA/IONO处理组和抑制剂Z-VRPR-FMK处理组;对照组不加入Z-VRPR-FMK和PMA/IONO处理,抑制剂Z-VRPR-FMK处理组和激动剂PMA/IONO处理组分别根据筛选的Z-VRPR-FMK最佳作用浓度和时间进行刺激培养,采用Western bloting法各组检测各组细胞中MALT1和A20蛋白的表达。结果:最适的ZVRPR-FMK作用浓度为75μmol/L、作用时间为0.5 h;与对照组相比,激动剂PMA/IONO处理组与抑制剂Z-VRPR-FMK处理组MALT1蛋白表达差异无统计学意义(P>0.05),但两组的A20蛋白表达均明显升高(P<0.01)。结论:抑制剂Z-VRPR-FMK能促进培养的Raji细胞内A20蛋白表达上调。 展开更多
关键词 淋巴瘤 细胞蛋白 MALT1 Z-vrpr-FMK
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Cloning and Functional Validation of Mung Bean VrPR Gene
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作者 Xiaokui Huang Yingbin Xue +3 位作者 Aaqil Khan Hanqiao Hu Naijie Feng Dianfeng Zheng 《Phyton-International Journal of Experimental Botany》 SCIE 2023年第8期2369-2382,共14页
For the purpose of functional validation,the mung bean(Vigna radiata)VrPR gene was cloned and overexpressed in Arabidopsis thaliana.Thefindings revealed that the ORF of VrPR contained 1200 bp,in which 399 amino acids w... For the purpose of functional validation,the mung bean(Vigna radiata)VrPR gene was cloned and overexpressed in Arabidopsis thaliana.Thefindings revealed that the ORF of VrPR contained 1200 bp,in which 399 amino acids were encoded.Bioinformatics analysis showed that the VrPR protein belonged to the NADB Rossmann superfamily,which was one of the non-transmembrane hydrophilic proteins.VrPR was assumed to have 44 amino acid phosphorylation sites and be contained in chloroplasts.The VrPR secondary structure comprised of random coil,αhelix,βangle,and extended chain,all of which were quite compatible with the anticipated tertiary structure.Moreover,analysis of the phylogenetic tree indicated that the soybean PR(Glyma.12G222200)and VrPR were closely related.Furthermore,chlorophyll content in leaves is markedly increased in Arabidopsis when VrPR is overexpressed.Ourfindings will serve as a reference for more functional studies on the PR genes in mung bean. 展开更多
关键词 Mung bean gene cloning vrpr transgenic arabidopsis functional verification
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