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从未感染和腺病毒2感染的细胞中分离出的细胞质和核膜复合物中的DNA结合蛋白。

DNA binding proteins in the cytoplasm and in a nuclear membrane complex isolated from uninfected and adenovirus 2 infected cells.

作者信息

Shanmugam G, Bhaduri S, Arens M, Green M

出版信息

Biochemistry. 1975 Jan 28;14(2):332-7. doi: 10.1021/bi00673a020.

Abstract

The DNA binding proteins in a nuclear membrane fraction that can synthesize DNA in vitro (referred to as "nuclear membrane complex") and in the cytoplasm of adenovirus infected and uninfected cells were isolated and characterized. Suspension cultures of human KB cells infected with human adenovirus 2 were treated with 25 mu-g/ml of arabinosylcytosine starting at 2 hr to block the synthesis of viral structural proteins, and then labeled with (3H)leucine from 6 to 24 hr after infection. Uninfected cells were treated similarly and labeled with (14C)leucine. The 3H-labeled proteins (infected cells) and 14C-labeled proteins (uninfected cells) isolated from the cytoplasm were mixed, as were the corresponding proteins isolated from the membrane complex, and each mixture was fractionated by stepwise elution from single-stranded DNA-cellulose columns. From 50 to 60% of the labeled protein in the membrane complex from infected cells and 40 to 50% of that from uninfected cells bound to DNA-cellulose in 0.05 M NaCl. Much less protein from the cytoplasm was bound to DNA cellulose, 20% from infected cells and 11% from uninfected cells. Gel electrophoresis of the mixture of 3H- and 14C-labeled proteins eluted from DNA-cellulose by different concentrations of NaCl revealed the following. (1) The 0.15 and 0.40 M NaCl eluates from the membrane complex of infected and uninfected cells contained a heterogenous mixture of similar polypeptides. (2) The 0.6 M NaCl eluate from the membrane complex derived from infected cells contained two major DNA binding proteins with molecular weights of 75,000 and 45,000 that were absent from uninfected cells. Large quantities of these two proteins were present in highly purified form in the 0.6 M NaCl eluate from the cytoplasm of infected cells. The DNA binding proteins of molecular weight 75,000 and 45,000 that are present in the cytoplasm are identical with those present in the membrane complex, as established by coelectrophoresis. (3) Two major cell-specific proteins of molecular weight 40,000 and 15,000-17,000 were present in the 2 M NaCl eluate of the membrane complex from uninfected and infected cells. A major cell-specific protein of molecular weight 33,000 was present in the 0.15 and 0.4 M NaCl eluates of the uninfected and infected cell cytoplasmic fractions. Aanalysis of cells labeled at 2-6 hr after infection in the absence of arabinosyl cytosine indicated that the synthesis of the DNA binding proteins of molecular weight 75,000 and 45,000 begins early after infection prior to the onset of viral DNA replication.

摘要

分离并鉴定了在体外能够合成DNA的核膜组分(称为“核膜复合物”)以及腺病毒感染和未感染细胞的细胞质中的DNA结合蛋白。用人腺病毒2感染的人KB细胞悬浮培养物,从感染后2小时开始用25μg/ml的阿糖胞苷处理,以阻断病毒结构蛋白的合成,然后在感染后6至24小时用(3H)亮氨酸进行标记。未感染的细胞进行类似处理并用(14C)亮氨酸进行标记。从细胞质中分离出的3H标记蛋白(感染细胞)和14C标记蛋白(未感染细胞)进行混合,从膜复合物中分离出的相应蛋白也进行混合,每种混合物通过从单链DNA - 纤维素柱上逐步洗脱进行分级分离。感染细胞的膜复合物中50%至60%的标记蛋白以及未感染细胞中40%至50%的标记蛋白在0.05M NaCl中与DNA - 纤维素结合。细胞质中与DNA纤维素结合的蛋白要少得多,感染细胞中为20%,未感染细胞中为11%。对用不同浓度NaCl从DNA - 纤维素上洗脱的3H和14C标记蛋白混合物进行凝胶电泳,结果如下:(1)感染和未感染细胞的膜复合物中0.15M和0.40M NaCl洗脱物含有相似多肽的异质混合物。(2)感染细胞来源的膜复合物中0.6M NaCl洗脱物含有两种主要的DNA结合蛋白,分子量分别为75,000和45,000,未感染细胞中不存在。在感染细胞细胞质的0.6M NaCl洗脱物中大量存在这两种高度纯化形式的蛋白。通过共电泳确定,细胞质中存在的分子量为75,000和45,000的DNA结合蛋白与膜复合物中的相同。(3)未感染和感染细胞的膜复合物的2M NaCl洗脱物中存在两种主要的细胞特异性蛋白,分子量分别为40,000和15,000 - 17,000。未感染和感染细胞细胞质组分的0.15M和0.4M NaCl洗脱物中存在一种主要的细胞特异性蛋白,分子量为33,000。对在感染后2 - 6小时在无阿糖胞苷情况下标记的细胞进行分析表明,分子量为75,000和45,000的DNA结合蛋白的合成在感染后早期、病毒DNA复制开始之前就开始了。

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