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Induction of mitochondrion-mediated apoptosis of CHO cells by tripchloro lide 被引量:11
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作者 yanren LEIXIONG JIARUIWU 《Cell Research》 SCIE CAS CSCD 2003年第4期295-300,共6页
Tripchlorolide (TC) is a potent antitumor reagent purified from a Chinese herb Tripterygium Wilfordii Hook. f.. However, its cellular effects and mechanism of action are unknown. We showed here that TC induced apoptos... Tripchlorolide (TC) is a potent antitumor reagent purified from a Chinese herb Tripterygium Wilfordii Hook. f.. However, its cellular effects and mechanism of action are unknown. We showed here that TC induced apoptosis of Chinese Hamster Ovary (CHO) cells in time- and dose-dependent manners. TC resulted in the degradation of Bcl-2, the translocation of Bax from the cytosol to mitochondria, and the release of cytochrome c from mitochondria. Stable overexpression of human Bcl-2 could reduce the apoptosis of TCtreated cells by blocking the translocation of Bax and the release of cytochrome c. These results indicate that TC induces apoptosis of CHO cell by activating the mitochondrion-mediated apoptotic pathway involving the proteins of Bcl-2 family and cytochrome c. 展开更多
关键词 APOPTOSIS mitochondrial pathway CHO cell.
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The C-Terminal Portion of the Nucleocapsid Protein Demonstrates SARS-CoV Antigenicity 被引量:4
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作者 GuozhenLiu ShaohuiHu +21 位作者 YongwuHu PengChen JianningYin JieWen JingqiangWang LiangLin JinxiuLiu BoYou YeYin ShutingLi HaoWang yanren JiaJi XiaoqianZhao YongqiaoSun XiaoweiZhang JianqiuFang JianWang SiqiLiu JunYu HengZhu HuanmingYang 《Genomics, Proteomics & Bioinformatics》 SCIE CAS CSCD 2003年第3期193-197,共5页
In order to develop clinical diagnostic tools for rapid detection of SARS-CoV (severe acute respiratory syndrome-associated coronavirus) and to identify candidate proteins for vaccine development, the C-terminal porti... In order to develop clinical diagnostic tools for rapid detection of SARS-CoV (severe acute respiratory syndrome-associated coronavirus) and to identify candidate proteins for vaccine development, the C-terminal portion of the nucleocapsid (NC) gene was amplified using RT-PCR from the SARS-CoV genome, cloned into a yeast expression vector (pEGH), and expressed as a glutathione S-transferase (GST) and Hisx6 double-tagged fusion protein under the control of an inducible promoter. Western analysis on the purified protein confirmed the expression and purification of the NC fusion proteins from yeast. To determine its antigenicity, the fusion protein was challenged with serum samples from SARS patients and normal controls. The NC fusion protein demonstrated high antigenicity with high specificity, and therefore, it should have great potential in designing clinical diagnostic tools and provide useful information for vaccine development. 展开更多
关键词 Severe Acute Respiratory Syndrome (SARS) CORONAVIRUS nucleocapsid protein ANTIGENICITY yeast expression system
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