Netzer K O, Schliephake A, Maurer B, Watanabe R, Aguzzi A, Rethwilm A
Institut für Virologie und Immunologie, Würzburg, Germany.
Virology. 1993 Jan;192(1):336-8. doi: 10.1006/viro.1993.1039.
Human foamy virus pol gene fragments were molecularly cloned into a procaryotic expression vector. The expression pattern of the cloned fragments and nucleotide sequence analysis of the 5' pol gene region revealed that in HFV the protease (PR) is located in the pol open reading frame. Purified recombinant proteins were used to generate antibodies in rats. In immunoblot assay, using infected cells as antigen, a precursor protein with an apparent molecular mass (M(r)) of 127K was identified by antibodies directed against the reverse transcriptase (RT), RNaseH, or integrase (IN) domains of pol. With concentrated virus as antigen, the RT and RNaseH antibodies recognized a protein of 80K, the IN antiserum recognized a protein of 40K, and the PR antiserum detected a protein of approximately 10K.
人泡沫病毒pol基因片段被分子克隆到原核表达载体中。对克隆片段的表达模式及pol基因5'区域的核苷酸序列分析表明,在人泡沫病毒中蛋白酶(PR)位于pol开放阅读框内。用纯化的重组蛋白在大鼠中制备抗体。在免疫印迹分析中,以感染细胞为抗原,针对pol的逆转录酶(RT)、核糖核酸酶H(RNaseH)或整合酶(IN)结构域的抗体鉴定出一种表观分子量(M(r))为127K的前体蛋白。以浓缩病毒为抗原,RT和RNaseH抗体识别出一种80K的蛋白,IN抗血清识别出一种40K的蛋白,PR抗血清检测到一种约10K的蛋白。