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石斑鱼虹彩病毒SGIV在宿主细胞内依赖微管运动的行为特征 被引量:1
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作者 王立群 王劭雯 +1 位作者 王宏达 秦启伟 《热带海洋学报》 CAS CSCD 北大核心 2020年第1期66-73,共8页
病毒是非常微小的简单生物,不能独立生存,必须借助宿主细胞完成自身的繁衍。病毒侵染进入细胞后,通常借助于微管通过黏稠的细胞质运动到特定的复制位点。然而,有关病毒依赖微管运动行为的精细动态研究还比较少。石斑鱼虹彩病毒(Singapor... 病毒是非常微小的简单生物,不能独立生存,必须借助宿主细胞完成自身的繁衍。病毒侵染进入细胞后,通常借助于微管通过黏稠的细胞质运动到特定的复制位点。然而,有关病毒依赖微管运动行为的精细动态研究还比较少。石斑鱼虹彩病毒(Singapore grouper iridovirus,SGIV)为虹彩病毒科蛙病毒属的一个新种,是海水养殖鱼类的重要病毒性病原,对海水养殖业造成重大经济损失。利用单粒子示踪技术实时追踪了SGIV病毒粒子沿微管运动的行为,观察到SGIV在细胞边缘至微管中心之间的双向运动,最高瞬时速度约0.2μm·s^–1,均表现为主动运输。病毒粒子运动至微管交叉位置会减速迂回,而后或受限于此,平均运动速率约0.008μm·s^–1,或通过交叉处继续快速运动,最高瞬时速度为0.2μm·s^–1。同时,SGIV感染会影响微管的形态结构,随着SGIV感染,微管逐渐围绕细胞核和病毒加工厂形成环状结构。研究结果初步揭示了SGIV病毒和细胞微管之间相互作用的复杂过程,丰富了我们对虹彩病毒胞内生命活动的认识,有助于深入地理解海水鱼类虹彩病毒感染致病机理。 展开更多
关键词 石斑鱼虹彩病毒 单粒子示踪技术 微管 病毒运输
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Intracellular transport of hepatitis B virus 被引量:6
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作者 Michael Kann André Schmitz Birgit Rabe 《World Journal of Gastroenterology》 SCIE CAS CSCD 2007年第1期39-47,共9页
For genome mulUplication hepadnaviruses use the transcriptional machinery of the cell that is found within the nucleus. Thus the viral genome has to be transported through the cytoplasm and nuclear pore. The intracyto... For genome mulUplication hepadnaviruses use the transcriptional machinery of the cell that is found within the nucleus. Thus the viral genome has to be transported through the cytoplasm and nuclear pore. The intracytosolic translocation is facilitated by the viral capsid that surrounds the genome and that interacts with cellular microtubules. The subsequent passage through the nuclear pore complexes (NPC) is mediated by the nuclear transport receptors importin α andβ. Importin α binds to the C-terminus of the capsid protein that comprises a nuclear localization signal (NLS). The exposure of the NLS is regulated and depends upon genome maturation and/or phosphorylation of the capsid protein. As for other karyophilic cargos using this pathway importin α interacts with importin β that facilitates docking of the import complex to the NPC and the passage through the pore. Being a unique strategy, the import of the viral capsid is incomplete in that it becomes arrested inside the nuclear basket, which is a cage-like structure on the karyoplasmic face of the NPC. Presumably only this compartment provides the factors that are required for capsid disassembly and genome release that is restricted to those capsids comprising a mature viral DNA genome. 展开更多
关键词 Hepatitis B virus CAPSID Intracellular transport MICROTUBULES Nuclear pore IMPORTIN Nuclear localization signal Nuclear basket
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The Nucleocytoplasmic Transport of Viral Proteins 被引量:2
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作者 Alan C. ZHENG 《Virologica Sinica》 SCIE CAS CSCD 2010年第2期79-85,共7页
Molecules can enter the nucleus by passive diffusion or active transport mechanisms, depending on their size. Small molecules up to size of 50-60 kDa or less than 10 nm in diameter can diffuse passively through the nu... Molecules can enter the nucleus by passive diffusion or active transport mechanisms, depending on their size. Small molecules up to size of 50-60 kDa or less than 10 nm in diameter can diffuse passively through the nuclear pore complex (NPC), while most proteins are transported by energy driven transport mechanisms Active transport of viral proteins is mediated by nuclear localization signals (NLS), which were first identified in Simian Virus 40 large T antigen and had subsequently been identified in a large number of viral they contain short stretches of lysine or arginine residues. These signals are recognized proteins. Usually by the importin super-family (importin α and β) proteins that mediate the transport across the nuclear envelope through Ran-GTP In contrast, only one class of the leucine-rich nuclear export signal (NES) on viral proteins is known at present. Chromosome region maintenance 1 (CRM1) protein mediates nuclear export of hundreds of viral proteins through the recognition of the leucine-rich NES. 展开更多
关键词 Nuclear localization signal (NLS) Nuclear export signal (NES) Nuclear pore complex (NPC) Viral proteins
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PcDNA3.1-GBD-壳聚糖纳米颗粒经鼻免疫小鼠的实验研究 被引量:2
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作者 江川 吴补领 苏凌云 《临床口腔医学杂志》 2004年第5期264-266,共3页
目的 :检测PcDAN 3 .1-GBD -壳聚糖纳米颗粒经鼻免疫小鼠的效果。方法 :制备两种PcDAN3 .1-GBD -壳聚糖纳米颗粒载体系统 ,经鼻黏膜免疫BALB/c小鼠 ,用间接ELISA法检测血清中针对葡聚糖结合蛋白A(GBD)的特异IgG抗体滴度及唾液中针对葡... 目的 :检测PcDAN 3 .1-GBD -壳聚糖纳米颗粒经鼻免疫小鼠的效果。方法 :制备两种PcDAN3 .1-GBD -壳聚糖纳米颗粒载体系统 ,经鼻黏膜免疫BALB/c小鼠 ,用间接ELISA法检测血清中针对葡聚糖结合蛋白A(GBD)的特异IgG抗体滴度及唾液中针对葡聚糖结合蛋白A(GBD)的特异IgA抗体滴度。与阳性对照组霍乱毒素 -PcDAN3 .1-GBD及未免疫组、空白壳聚糖纳米颗粒组作比较。结果 :该载体系统经鼻免疫小鼠所产生的血清及唾液中针对GBD的IgG和IgA抗体滴度远大于未免疫组和空白壳聚糖纳米颗粒组 ,而与阳性对照组霍乱毒素-PcDAN3 .1-GBD组抗体滴度相当。且维持的抗体滴度更稳定和持久。结论 :壳聚糖纳米颗粒系统可作为经鼻运输基因防龋疫苗的载体系统。 展开更多
关键词 PcDAN3.1-GBD 壳聚糖纳米颗粒 ELISA 免疫 病毒基因运输
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