Damsky C H, Sheffield J B, Tuszynski G P, Warren L
J Cell Biol. 1977 Nov;75(2 Pt 1):593-605. doi: 10.1083/jcb.75.2.593.
Electrophoretic data from both sodium dodecyl sulfate-polyacrylamide gels (SDS-PAGE) and acid-urea gels reveal a protein in purified murine mammary tumor virus (MuMTV) which co-migrates with purified chick skeletal muscle actin. 125I-labeling of intact and disrupted virus preparations shows that the actin-like protein is not artifactually adsorbed to the outside of virions during isolation. Quantitative SDS-PAGE and examination of negatively stained preparations show that the actin cannot be accounted for by a contaminating population of virus-free vesicles. The ultrastructure of mammary epithelial cells and of Rous sarcoma virus-transformed chick embryo fibroblasts shows that virus extrusion is associated with filament-containing cellular processes. In particular, MuMTV is released from the ends of long microvilli which contain a bundle of 6-8-nm microfilaments and share other structural features with intestinal microvilli. We suggest that virus nucleoids require an interaction with host cell contractile proteins for their extrusion from the cell.
来自十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和酸性尿素凝胶的电泳数据显示,在纯化的鼠乳腺肿瘤病毒(MuMTV)中有一种蛋白质,它与纯化的鸡骨骼肌肌动蛋白迁移率相同。对完整和破碎病毒制剂进行¹²⁵I标记表明,在分离过程中,类肌动蛋白并非人为吸附在病毒粒子外部。定量SDS-PAGE和对负染制剂的检查表明,肌动蛋白不能用不含病毒的囊泡污染群体来解释。乳腺上皮细胞和劳氏肉瘤病毒转化的鸡胚成纤维细胞的超微结构表明,病毒的挤出与含有细丝的细胞过程有关。特别是,MuMTV从长微绒毛的末端释放,这些微绒毛含有一束6-8纳米的微丝,并且与肠道微绒毛具有其他结构特征。我们认为病毒核样物从细胞中挤出需要与宿主细胞收缩蛋白相互作用。