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新Poly+A+RNA结合蛋白Kazrin可能参与细胞内mRNA转运和定位.pdf49页
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天津置科大掌硬士掌位论文
mRNA胞内运输和定位是真核基因表达调控的重要一环,依赖细胞骨架特别
是微管系统的主动运输是其中最重要的机制。mRNA如何与马达蛋白 momr
protein 相互作用一直困扰着研究人员,我们已经找到一个能够即结合驱动蛋白
轻链 1dnesinlie;llt
与什么RNA相互作用还不清楚,本研究寻找并确定与蛐相互作用的核酸序
列,探索性研究kazrin在细胞中mRNA转运与定位中的可能作用。
白,与鼠胚和鼠脑总RNA体外结合反应,酚氯仿抽提靶RNA,
正在加载中,请稍后...Development of influenza H7N9 virus like particle (VLP) vaccine: ho...
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2013 Sep 13;31(40):4305-13. doi: 10.1016/j.vaccine.. Epub
2013 Jul 26.Development of influenza H7N9 virus like particle (VLP) vaccine: homologous A/Anhui/1/2013 (H7N9) protection and heterologous A/chicken/Jalisco/CPA1/2012 (H7N3) cross-protection in vaccinated mice challenged with H7N9 virus.1, , , , , , , , , .1Novavax, Inc., 9920 Belward Campus Drive, Rockville, MD 20850, USA. AbstractThe recent emergence of severe human illness caused by avian-origin influenza A(H7N9) viruses in China has precipitated a global effort to rapidly develop and test vaccine candidates. To date, non-A(H7N9) H7 subtype influenza vaccine candidates have been poorly immunogenic and difficulties in production of A(H7N9) virus seed strains have been encountered. A candidate recombinant A(H7N9) vaccine consisting of full length, unmodified hemagglutinin (HA) and neuraminidase (NA) from the A/Anhui/1/2013 and the matrix 1 (M1) protein from the A/Indonesia/05/2005 (H5N1) were cloned into a baculovirus vector. Baculovirus infected Spodoptera frugiperda (Sf9) insect cells secreted virus like particles (VLP) composed of HA, NA, and M1 that resemble mature influenza virions. Genetic construction of vaccine from acquisition of an H7N9 genomic sequence to production of A(H7N9) VLP occurred in 26 days. The immunogenicity and efficacy of A/Anhui/1/2013 (H7N9) VLP vaccine administered on days 0 and 14 were evaluated in a lethal wild-type challenge Balb/c mouse model. Control groups included a non-homologous H7 vaccine (A/chicken/Jalisco/CPA1/2012 (H7N3)-VLP), and A/Indonesia/05/2005 (H5N1)-VLP, or placebo. All vaccines were administered with or without ISCOMATRIX. A(H7N9) VLP elicited hemagglutination-inhibition (HAI) antibody titers of ≥ 1:64 against the homologous virus, cross-reactive HAI against the heterologous A(H7N3), and 3- to 4-fold higher HAI responses in corresponding ISCOMATRIX subgroups. Similarly, all doses of H7N9 VLP elicited anti-neuraminidase (NA) antibody, with 3- to 4-fold higher responses measured in the corresponding ISCOMATRIX subgroups. The non-homologous H7 vaccine induced both H7N3 and H7N9 HAI but no N9 anti-NA antibodies. A lethal murine wild-type A/Anhui/1/2013 (H7N9) challenge demonstrated 100% survival of all animals receiving A(H7N9) and A(H7N3) vaccine, versus 0% survival in A(H5N1) vaccine and placebo groups. Together, the data demonstrate that recombinant H7N9 vaccine can be rapidly developed that was immunogenic and efficacious supporting testing in man as a pandemic influenza H7N9 vaccine candidate.Copyright (C) 2013 The Authors. Published by Elsevier Ltd.. All rights reserved.KEYWORDS: H7N9; H I P V Virus like particlePMID:
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