Mortara R A, Koch G L
Medical Research Council, Laboratory of Molecular Biology, Cambridge, U.K.
J Submicrosc Cytol Pathol. 1989 Apr;21(2):295-306.
Mammalian cells infected with retroviruses frequently display virus particles budding at the tip of cellular projections resembling microvilli and filopodia. In normal and infected cells these cellular projections contain actin microfilaments and in specialized retrovirus-tipped projections from the P815 cell, a direct association between actin filaments and the apical virus particle could be demonstrated (Mortara and Koch, 1986). Here we confirm and extend these observations using a murine macrophage cell line chronically infected with a C-type retrovirus. Immunochemical and biochemical methods were used to identify actin-associated and actin-binding components among the retroviral polypeptides. The results show that Pr65gag and its p15 N-terminal domain can bind to actin in vitro and may be major binding sites for actin filaments on the retroviral nucleocapsid.
感染逆转录病毒的哺乳动物细胞常常会出现病毒粒子在类似微绒毛和丝状伪足的细胞突起尖端出芽的现象。在正常细胞和受感染细胞中,这些细胞突起含有肌动蛋白微丝,并且在源自P815细胞的特殊逆转录病毒尖端突起中,可以证明肌动蛋白丝与顶端病毒粒子之间存在直接关联(莫尔塔拉和科赫,1986年)。在此,我们使用长期感染C型逆转录病毒的小鼠巨噬细胞系证实并扩展了这些观察结果。采用免疫化学和生化方法来鉴定逆转录病毒多肽中与肌动蛋白相关及结合肌动蛋白的成分。结果表明,Pr65gag及其p15 N端结构域在体外可与肌动蛋白结合,可能是逆转录病毒核衣壳上肌动蛋白丝的主要结合位点。