Studies on ZAP, a broad-spectrum alphavirus inhibitor

广谱甲病毒抑制剂ZAP的研究

• 批准号: 7019145
• 负责人: MARGARET R MACDONALD
• 金额: $ 37.13万
• 依托单位: ROCKEFELLER UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-03-01 至 2010-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7019145
• 关键词: Alphavirus; RNA binding protein; Sindbis virus; antiviral agents; host organism interaction; laboratory mouse; messenger RNA; nucleic acid quantitation /detection; posttranscriptional RNA processing; protein structure; protein structure function; virus RNA; virus infection mechanism; virus replication

DESCRIPTION (provided by applicant): Infection by viruses in the Togaviridae family causes significant worldwide morbidity and mortality. There is currently no specific treatment for patients infected with any virus from this family. Viruses in the Alphavirus genus cause diseases ranging from fever, rash and arthritis to fatal encephalitis. Several members of this genus have been identified as possible agents of bioterrorism. Our preliminary studies indicate that the rat zinc-finger antiviral protein (ZAP), which was originally discovered as a host protein that inhibits replication of retroviruses, potently inhibits replication of multiple members of the Alphavirus genus. Sindbis virus (SIN), Ross River virus, Semliki Forest virus and Venezuelan equine encephalitis virus replication were all inhibited to varying extents. The long-term objectives of this project are to elucidate, using virological, molecular and cell biological approaches, the mechanism(s) by which ZAP inhibits replication of alphaviruses. Investigations using SIN, which has been studied extensively and is dramatically inhibited by ZAP, show that replication is blocked after entry and at or before translation of the incoming plus strand genomic viral RNA. Experiments outlined in this proposal will determine the relationship between ZAP levels and SIN replication, and will investigate the mechanism by which ZAP blocks SIN RNA translation. We will characterize the interaction between ZAP and the SIN RNA, as well as the interaction, if any, between ZAP and other host or viral factors. Understanding the mechanism of ZAP's inhibition of alphavirus replication may lead to the development of new therapeutic or preventative agents for illness due to alphavirus infection.

描述（由申请方提供）：披膜病毒科病毒感染导致全球范围内的显著发病率和死亡率。目前没有针对感染该家族任何病毒的患者的特异性治疗方法。甲病毒属的病毒引起的疾病范围从发烧、皮疹和关节炎到致命的脑炎。该属的几个成员已被确定为生物恐怖主义的可能代理人。我们的初步研究表明，大鼠锌指抗病毒蛋白（ZAP），这是最初发现的宿主蛋白，抑制逆转录病毒的复制，有效地抑制多个成员的甲病毒属的复制。辛德毕斯病毒（SIN）、罗斯河病毒、塞姆利基森林病毒和委内瑞拉马脑炎病毒的复制均受到不同程度的抑制。该项目的长期目标是使用病毒学、分子和细胞生物学方法阐明ZAP抑制甲病毒复制的机制。使用SIN的研究，已被广泛研究，并显着抑制ZAP，显示复制被阻断后进入和翻译的传入正链基因组病毒RNA或之前。本提案中概述的实验将确定ZAP水平与SIN复制之间的关系，并将研究ZAP阻断SIN RNA翻译的机制。我们将描述ZAP和SIN RNA之间的相互作用，以及ZAP和其他宿主或病毒因子之间的相互作用。了解ZAP抑制甲病毒复制的机制可能会导致开发新的治疗或预防剂，用于治疗甲病毒感染引起的疾病。