Qi Y J, Zhou X P, Huang X Z, Li G X
Institute of Biotechnology, Zhejiang University, Hangzhou, PR China.
Arch Virol. 2002 May;147(5):917-28. doi: 10.1007/s00705-001-0782-2.
The VP37 protein encoded by the RNA2 of Broad bean wilt virus 2 (BBWV2) was overexpressed in Escherichia coli. The protein was purified and a polyclonal antibody specific for the protein was produced. Time course studies by Western blot assays in BBWV2-infected Chenopodium quinoa leaves showed that the VP37 protein was present in cells of the inoculated leaves by 12 h post inoculation and in cells of systemically-infected leaves by 2 days post inoculation. The protein was able to accumulate to a high level in infected leaves at the late infection stage. Gel retardation and UV cross-linking assays demonstrated that the VP37 protein bound preferentially single-stranded (ss) RNA and DNA in a non-sequence-specific manner. The VP37 protein-RNA complex was stable in solutions containing less than 400 mM NaCl, but became fully dissociated in the solutions containing 800 mM NaCl. Sequence analysis of the VP37 protein and its ability to bind ssRNA and ssDNA suggest that the protein may play a role similar to the movement proteins reported for other plant viruses.
蚕豆萎蔫病毒2(BBWV2)的RNA2编码的VP37蛋白在大肠杆菌中过表达。该蛋白经纯化后制备了针对该蛋白的多克隆抗体。通过蛋白质免疫印迹分析对感染BBWV2的藜麦叶片进行的时间进程研究表明,接种后12小时,接种叶片的细胞中存在VP37蛋白,接种后2天,系统感染叶片的细胞中存在该蛋白。在感染后期,该蛋白能够在感染叶片中积累到高水平。凝胶阻滞和紫外线交联分析表明,VP37蛋白以非序列特异性方式优先结合单链(ss)RNA和DNA。VP37蛋白-RNA复合物在含有低于400 mM NaCl的溶液中稳定,但在含有800 mM NaCl的溶液中完全解离。VP37蛋白的序列分析及其结合ssRNA和ssDNA的能力表明,该蛋白可能发挥与其他植物病毒报道的运动蛋白类似的作用。