首页> 美国卫生研究院文献>Journal of Virology >Interaction with Coxsackievirus and Adenovirus Receptor but Not with Decay-Accelerating Factor (DAF) Induces A-Particle Formation in a DAF-Binding Coxsackievirus B3 Isolate
【2h】

Interaction with Coxsackievirus and Adenovirus Receptor but Not with Decay-Accelerating Factor (DAF) Induces A-Particle Formation in a DAF-Binding Coxsackievirus B3 Isolate

机译:与柯萨奇病毒和腺病毒受体的相互作用但不与衰变加速因子(DAF)相互作用在结合DAF的柯萨奇病毒B3分离物中诱导A颗粒形成。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Although many coxsackie B viruses interact with decay accelerating factor (DAF), attachment to DAF by itself is not sufficient to initiate infection. We examined the early events in infection that follow virus interaction with DAF, and with the coxsackievirus and adenovirus receptor (CAR). Interaction with soluble CAR in a cell-free system, or with CAR on the surfaces of transfected cells, induced the formation of A particles; interaction with soluble or cell surface DAF did not. The results suggest that CAR, but not DAF, is capable of initiating the conformational changes in the viral capsid that lead to release of viral nucleic acid.
机译:尽管许多柯萨奇B病毒与衰变加速因子(DAF)相互作用,但仅依附于DAF不足以引发感染。我们检查了病毒与DAF以及与柯萨奇病毒和腺病毒受体(CAR)相互作用后感染的早期事件。在无细胞系统中与可溶性CAR相互作用,或在转染细胞表面与CAR相互作用,诱导了A颗粒的形成。与可溶性或细胞表面DAF的相互作用没有。结果表明,CAR(而不是DAF)能够引发病毒衣壳中导致病毒核酸释放的构象变化。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号