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Aerodynamics analysis of a hypersonic electromagnetic gun launched projectile 被引量:3
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作者 Jian Shen Shao-bo Fan +2 位作者 Ya-xin Ji qing-yu zhu Ji Duan 《Defence Technology(防务技术)》 SCIE EI CAS CSCD 2020年第4期753-761,共9页
A hypersonic aerodynamics analysis of an electromagnetic gun(EM gun) launched projectile configuration is undertaken in order to ameliorate the basic aerodynamic characteristics in comparison with the regular projecti... A hypersonic aerodynamics analysis of an electromagnetic gun(EM gun) launched projectile configuration is undertaken in order to ameliorate the basic aerodynamic characteristics in comparison with the regular projectile layout.Static margin and pendulum motion analysis models have been applied to evaluate the flight stability of a new airframe configuration.With a steady state computational fluid dynamics(CFD) simulation,the basic density,pressure and velocity contours of the EM gun projectile flow field at Mach number 5.0,6.0 and 7.0(angle of attack=0°) have been analyzed.Furthermore,the static margin values are enhanced dramatically for the EM gun projectile with configuration optimization.Drag,lift and pitch property variations are all illustrated with the changes of Mach number and angle of attack.A particle ballistic calculation was completed for the pendulum analysis.The results show that the configuration optimized projectile,launched from the EM gun at Mach number 5.0 to 7.0,acts in a much more stable way than the projectiles with regular aerodynamic layout. 展开更多
关键词 Electromagnetic gun launched projectile Hypersonic aerodynamics Airframe configuration optimization Static margin PENDULUM
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Receptor-binding domain of SARS-Cov spike protein: Soluble expression in E.coli, purification and functional characterization 被引量:1
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作者 Jing Chen Lin Miao +5 位作者 Jia-Ming Li Yan-Ying Li qing-yu zhu Chang-Lin Zhou Hong-Qing Fang Hui-Peng Chen 《World Journal of Gastroenterology》 SCIE CAS CSCD 2005年第39期6159-6164,共6页
瞄准:日冕病毒的尖铁蛋白质为病毒绑定,熔化和入口负责,并且是中和抗体的主要 inducer。这篇论文是发现严重尖锐呼吸联系症候群的日冕病毒(SARS-Cov ) 的一个可溶、功能的 recombinant 受体绑定领域,并且分析它的受体绑定能力。方... 瞄准:日冕病毒的尖铁蛋白质为病毒绑定,熔化和入口负责,并且是中和抗体的主要 inducer。这篇论文是发现严重尖锐呼吸联系症候群的日冕病毒(SARS-Cov ) 的一个可溶、功能的 recombinant 受体绑定领域,并且分析它的受体绑定能力。方法:三个熔化标签(谷胱甘肽 S-transferase, GST;thioredoxin, Trx;麦芽糖绑定蛋白质, MBP ) ,它最好贡献增加的溶解度并且到便于异种蛋白质的合适的合拢,被用来在埃希氏杆菌属关口 i 获得 RBD 蛋白质的可溶、功能的表示(BL21 (DE3 ) 和 Rosetta-gamiB (DE3 ) 拉紧) 。净化的可溶的 RBD 蛋白质的受体绑定能力然后被 ELISA 和流动血细胞计数试金检测。结果:当在许多不同文化和正式就职条件下面在 BL21 (DE3 ) 和 Rosetta-gamiB (DE3 ) 作为 TrxA 标签形式熔化了时, SARS-Cov 尖铁蛋白质的 RBD 被表示为包括身体。并且当 RBD 被表示时,当 MBP 标注了形式, SDS 页上没有可见表示乐队。仅仅 GST 标注了 RBD 是可溶的在 BL21 (DE3 ) 表示了,并且蛋白质被巢菜净化主要层析系统。ELISA 数据证明那 GST/RBD 抗原带着 anti-RBD 老鼠有阳性反应单音的同种细胞的抗体 1A5。进一步的流动血细胞计数试金表明了 RBD ACE2 的有约束力的能力的高效率(变换血管收缩素的酶 2 ) 积极 Vero E6 房间。并且 ACE2 与 SARS-Cov 尖铁蛋白质作为反省的细胞的受体被证明一个起始亲密关系的相互作用。到 Vero E6 房间的 GST 和 GST/RBD 绑定的几何平均数分别地是 77.08 和 352.73。结论:在这篇论文,我们得到标注 RBD 蛋白质在 E.coli BL21 (DE3 ) 表示了的足够的可溶的 N 终端 GST;从 ELISA 和流动血细胞计数试金的数据证明 recombinant 蛋白质高效地对 ACE2 积极 Vero E6 房间功能、有约束力。并且从 E.coli 导出的 recombinant RBD 能习惯于与受体开发对块 S 蛋白质绑定疫苗的子单元并且到抵销 SARS-Cov 感染。 展开更多
关键词 SARS 非典型性肺炎 大肠杆菌 血液净化 治疗方法
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Construction and Genetic Analysis of Murine Hepatitis Virus Strain A59 Nsp16 Temperature Sensitive Mutant and the Revertant Virus
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作者 Guo-hui Chang Bao-jun Luo +5 位作者 Pin Lu Lei Lin Xiao-yan Wu Jing Li Yi Hu qing-yu zhu 《Virologica Sinica》 SCIE CAS CSCD 2011年第1期19-29,共11页
Coronaviruses (CoVs) are generally associated with respiratory and enteric infections and have long been recognized as important pathogens of livestock and companion animals. Mouse hepatitis virus (MHV) is a widely st... Coronaviruses (CoVs) are generally associated with respiratory and enteric infections and have long been recognized as important pathogens of livestock and companion animals. Mouse hepatitis virus (MHV) is a widely studied model system for Coronavirus replication and pathogenesis. In this study,we created a MHV-A59 temperature sensitive (ts) mutant Wu"-ts18(cd) using the recombinant vaccinia reverse genetics system. Virus replication assay in 17C1-1 cells showed the plaque phenotype and replication characterization of constructed Wu"-ts18(cd) were indistinguishable from the reported ts mutant Wu"-ts18. Then we cultured the ts mutant Wu"-ts18(cd) at non-permissive temperature 39.5°C,which "forced" the ts recombinant virus to use second-site mutation to revert from a ts to a non-ts phenotype. Sequence analysis showed most of the revertants had the same single amino acid mutation at Nsp16 position 43. The single amino acid mutation at Nsp16 position 76 or position 130 could also revert the ts mutant Wu"-ts18 (cd) to non-ts phenotype,an additional independent mutation in Nsp13 position 115 played an important role on plaque size. The results provided us with genetic information on the functional determinants of Nsp16. This allowed us to build up a more reasonable model of CoVs replication-transcription complex. 展开更多
关键词 小鼠肝炎病毒 温度敏感 突变体 遗传分析 逆转 模型系统 重组痘苗病毒 反向遗传学
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Establishment of the Eukaryotic Cell Lines for Inducible Control of SARS-CoV Nucleocapsid Gene Expression
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作者 Guo-hui CHANG Andrew Dividson +3 位作者 Lei LIN Matt Wilson Stuart G Siddell qing-yu zhu 《Virologica Sinica》 SCIE CAS CSCD 2010年第5期361-368,共8页
In order to establish the eukaryotic cell lines for inducible control of SARS-CoV nucleocapsid gene expression.The recombinant plasmid of pTRE-Tight-SARS-N was constructed by using the plasmid p8S as the PCR template ... In order to establish the eukaryotic cell lines for inducible control of SARS-CoV nucleocapsid gene expression.The recombinant plasmid of pTRE-Tight-SARS-N was constructed by using the plasmid p8S as the PCR template which contains a cDNA clone covering the nucleocapsid gene of SARS-CoV HKU-39449. Restriction enzymes digestion and sequence analysis indicated the recombinant plasmid of pTRE-Tight-SARS-N contained the nucleocapsid gene with the optimized nucleotide sequence which will improve the translation efficiency. Positive cell clones were selected by cotransfecting pTRE-Tight-SARS-N with the linear marker pPUR to BHK-21 Tet-on cells in the presence of puromycin. A set of double-stable eukaryotic cell lines (BHK-Tet-SARS-N) with inducible control of the SARS-CoV neucleocapsid gene expression was identified by using SDS-PAGE and Western-blot analysis. The expression of SARS-CoV nucleocapsid protein was tightly regulated by the varying concentration of doxcycline in the constructed double-stable cell line. The constructed BHK-Tet-SARS-N cell strains will facilitate the rescue of SARS-CoV in vitro and the further reverse genetic research of SARS-CoV. 展开更多
关键词 核衣壳蛋白基因 SARS病毒 真核细胞表达 基因表达 诱导控制 细胞系 SARS冠状病毒 cDNA克隆
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