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首页> 外文期刊>Antiviral Research >Specific ligands for classical swine fever virus screened from landscape phage display library
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Specific ligands for classical swine fever virus screened from landscape phage display library

机译:从景观噬菌体展示库筛选经典猪瘟病毒的特异性配体

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摘要

Classical swine fever (CSF) is a devastating infectious disease caused by classical swine fever virus (CSFV). The screening of CSFV-specific ligands is of great significance for diagnosis and treatment of CSF. Affinity selection from random peptide libraries is an efficient approach to discover ligands with high stability and specificity. Here, we screened phage ligands for the CSFV E2 protein from f8/8 landscape phage display library by biopanning and obtained four phage clones specific for the E2 protein of CSFV. Viral blocking assays indicated that the phage clone displaying the octapeptide sequence DRATSSNA remarkably inhibited the CSFV replication in PK-15 cells at a titer of 1010 transduction units, as evidenced by significantly decreased viral RNA copies and viral titers. The phage-displayed E2-binding peptides have the potential to be developed as antivirals for CSF.
机译:古典猪瘟(CSF)是由古典猪瘟病毒(CSFV)引起的毁灭性传染病。 CSFV特异性配体的筛选对CSF的诊断和治疗具有重要意义。从随机肽库中进行亲和力选择是发现具有高稳定性和特异性的配体的有效方法。在这里,我们通过生物淘选从f8 / 8景观噬菌体展示文库中筛选了CSFV E2蛋白的噬菌体配体,并获得了对CSFV E2蛋白具有特异性的四个噬菌体克隆。病毒阻断试验表明,展示八肽序列DRATSSNA的噬菌体克隆以1010转导单位的效价显着抑制PK-15细胞中的CSFV复制,这通过病毒RNA拷贝和病毒效价的显着降低得以证明。噬菌体展示的E2结合肽有可能被开发为CSF的抗病毒药。

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