首页> 美国卫生研究院文献>Journal of Virology >Adenovirus early region 1B 58000-dalton tumor antigen is physically associated with an early region 4 25000-dalton protein in productively infected cells.
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Adenovirus early region 1B 58000-dalton tumor antigen is physically associated with an early region 4 25000-dalton protein in productively infected cells.

机译:腺病毒早期区域1B 58000道尔顿的肿瘤抗原与生产性感染细胞中早期区域4 25000道尔顿的蛋白质物理相关。

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摘要

In soluble protein extracts obtained from adenovirus productively infected cells, monoclonal antibodies directed against the early region 1B 58,000-dalton (E1B-58K) protein immunoprecipitated, in addition to this protein, a polypeptide of 25,000 molecular weight. An analysis of tryptic peptides derived from this 25K protein demonstrated that it was unrelated to the E1B-58K protein. The tryptic peptide maps of the 25K protein produced in adenovirus 5 (Ad5)-infected HeLa cells and BHK cells were identical, whereas Ad3-infected HeLa cells produced a different 25K protein. The viral origin of this 25K protein was confirmed by an amino acid sequence determination of five methionine residues in two Ad2 tryptic peptides derived from the 25K protein. The positions of these methionine residues in the 25K protein were compared with the nucleotide sequence of Ad2 and uniquely mapped the gene for this protein to early region 4, subregion 6 of the viral genome. A mutant of Ad5 was obtained (Ad5 dl342) which failed to produce detectable levels of the E1B-58K protein. In HeLa cells infected with this mutant, monoclonal antibodies directed against the E1B-58K protein failed to detect the associated 25K protein. In 293 cells infected with Ad5 dl342, which contain an E1B-58K protein encoded by the integrated adenovirus genome, the mutant produced an E4-25K protein which associated with the E1B-58K protein derived from the integrated genome. Extracts of labeled Ad5 dl342-infected HeLa cells (E1B-58K-) were mixed in vitro with extracts of unlabeled Ad5 wild type-infected HeLa cells or 293 cells (E1B-58K+). When the mixed extracts were incubated with the E1B-58K monoclonal antibody, a labeled E4-25K protein was coimmunoprecipitated. When extracts of Ad5 dl342-infected HeLa cells and uninfected HeLa cells (both E1B-58K-) were mixed, the E1B-58K monoclonal antibody failed to immunoselect the E4-25K protein. These data provide evidence that the E1B-58K antigen is physically associated with an E4-25K protein in productively infected cells. This is the same E1B-58K protein that was previously shown to be associated with the cellular p53 antigen in adenovirus-transformed cells.
机译:在从腺病毒生产性感染细胞中获得的可溶性蛋白质提取物中,针对早期1B 58,000道尔顿(E1B-58K)蛋白的单克隆抗体除该蛋白外,还免疫沉淀了25,000分子量的多肽。对源自该25K蛋白的胰蛋白酶肽的分析表明,它与E1B-58K蛋白无关。在感染了腺病毒5(Ad5)的HeLa细胞和BHK细胞中产生的25K蛋白的胰蛋白酶肽图是相同的,而感染Ad3的HeLa细胞则产生了不同的25K蛋白。通过氨基酸序列确定了两个25K蛋白衍生的两个Ad2胰蛋白酶肽中的五个蛋氨酸残基,从而证实了该25K蛋白的病毒起源。将这些蛋氨酸在25K蛋白中的位置与Ad2的核苷酸序列进行比较,并将该蛋白的基因独特地定位到病毒基因组的早期区域4,子区域6。获得了不能产生可检测水平的E1B-58K蛋白的Ad5突变体(Ad5 dl342)。在感染了该突变体的HeLa细胞中,针对E1B-58K蛋白的单克隆抗体未能检测到相关的25K蛋白。在被Ad5 dl342感染的293细胞中,该细胞含有由整合的腺病毒基因组编码的E1B-58K蛋白,该突变体产生了与源自整合的基因组的E1B-58K蛋白相关的E4-25K蛋白。将标记的Ad5 dl342感染的HeLa细胞(E1B-58K-)的提取物与未标记的Ad5野生型感染的HeLa细胞或293细胞(E1B-58K +)的提取物进行体外混合。当混合提取物与E1B-58K单克隆抗体一起孵育时,标记的E4-25K蛋白被共免疫沉淀。将感染Ad5 dl342的HeLa细胞和未感染的HeLa细胞(均为E1B-58K-)的提取物混合时,E1B-58K单克隆抗体无法免疫选择E4-25K蛋白。这些数据提供了证据,证明E1B-58K抗原与生产性感染细胞中的E4-25K蛋白物理相关。这与以前显示与腺病毒转化细胞中的细胞p53抗原相关的E1B-58K蛋白相同。

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