Identification of RNA replicase subunits responsible for initiation of RNA synthesis of tick-borne encephalitis virus by affinity labelling.

Biomedical science Pub Date : 1991-01-01
O V Morozova, N A Belyavskaya, E F Zaychikov, E A Kvetkova, A A Mustaev, A G Pletnev
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Abstract

Porcine embryo kidney cells infected by tick-borne encephalitis virus (TBEV) were fractionated into nuclear, membrane, and cytoplasmic fractions. To identify proteins involved in the initiation of RNA replication at different stages of infection a highly specific affinity labelling technique was used. In samples of the nuclear fraction taken from cells 45 h after infection (late stage), affinity labelling with aldehyde-containing derivatives of ATP and elongation of this label with [alpha-32P]GTP identified a polypeptide with a molecular mass of about 69 kDa. By means of affinity labelling with aldehyde-containing analogues of GMP, GDP, and GTP as initiation substrates and [alpha-32P]ATP as the elongation substrate, a polypeptide of 100 kDa was selectively modified in the nuclear fraction of cells at the early stages of infection (8 h). These proteins were immunostained with TBEV-specific antibodies, and were identified as the nonstructural TBEV proteins NS3 and NS5, respectively. It was concluded that NS3 and NS5 take part in the initiation of TBEV genome replication at the late and early stages of infection, respectively.

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用亲和标记法鉴定蜱传脑炎病毒启动RNA合成的RNA复制酶亚基。
将感染蜱传脑炎病毒(TBEV)的猪胚肾细胞分离成核、膜和细胞质部分。为了鉴定在感染的不同阶段参与RNA复制起始的蛋白质,使用了一种高度特异性的亲和标记技术。在感染后45小时(晚期)取自细胞的核部分样本中,用含醛的ATP衍生物进行亲和标记,并用[α - 32p]GTP延长该标记,鉴定出分子量约为69 kDa的多肽。通过以含醛的GMP、GDP和GTP类似物作为起始底物,以[α - 32p]ATP作为延伸底物的亲和标记,在感染早期(8 h)的细胞核部分选择性修饰了一个100 kDa的多肽。这些蛋白用TBEV特异性抗体免疫染色,分别鉴定为非结构性TBEV蛋白NS3和NS5。由此可见,NS3和NS5分别在感染后期和早期参与了TBEV基因组复制的启动。
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