Gambke C, Deppert W
J Virol. 1981 Nov;40(2):585-93. doi: 10.1128/JVI.40.2.585-593.1981.
We analyzed the subcellular locations of the late adenovirus type 2 nonstructural 100,000-dalton (100K) and 33K proteins in adenovirus type 2-infected HeLa cells both by biochemical cell fractionation and by immunofluorescence microscopy, using specific antisera against purified sodium dodecyl sulfate-denatured 100K and 33K polypeptides. Both methods showed that the 100K protein was present in the cytoplasm as well as in the nuclei of infected cells and that it accumulated in the nuclei during the course of infection. Phosphorylated 100K protein also was found both in the cytoplasm and in nuclei. However, the nuclear 100K protein pool was phosphorylated to a higher degree than the cytoplasmic pool. In all experiments the 33K protein, which also is a phosphoprotein, was present exclusively in the nuclei of infected cells. The 100K and 33K proteins were associated with different nuclear substructures; this was demonstrated serologically by an analysis of infected cells in which double color immunofluorescence microscopy was used. In these experiments antibodies against the 100K protein decorated different nuclear structures than antibodies against the 33K protein.
我们通过生化细胞分级分离和免疫荧光显微镜技术,利用针对纯化的十二烷基硫酸钠变性的100K和33K多肽的特异性抗血清,分析了2型腺病毒感染的HeLa细胞中2型腺病毒晚期非结构100,000道尔顿(100K)和33K蛋白的亚细胞定位。两种方法均显示,100K蛋白存在于受感染细胞的细胞质和细胞核中,并且在感染过程中在细胞核中积累。磷酸化的100K蛋白也在细胞质和细胞核中被发现。然而,核内100K蛋白池的磷酸化程度高于细胞质池。在所有实验中,同样作为磷蛋白的33K蛋白仅存在于受感染细胞的细胞核中。100K和33K蛋白与不同的核亚结构相关;通过对使用双色免疫荧光显微镜的受感染细胞进行分析,血清学证明了这一点。在这些实验中,针对100K蛋白的抗体与针对33K蛋白的抗体所标记的核结构不同。