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首页> 外文期刊>Nucleic acids research >Detection of a cellular polypeptide associated with adenovirus-coded VA RNA using in vitro labeling of proteins cross-linked to RNA
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Detection of a cellular polypeptide associated with adenovirus-coded VA RNA using in vitro labeling of proteins cross-linked to RNA

机译:检测与腺病毒编码的VA RNA相关的细胞多肽,使用与RNA交联的蛋白质的体外标记

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摘要

Ultraviolet light induced RNA-protein cross-linking for identification of polypeptides interacting with RNA in intact cells (wagenmakers et al. 1980), is limited by the intensity of the label in the proteins or in residual nucleotides remaining attached to the proteins after RNase treatment of the RNA-protein complexes. Here we report a method, where the cross-linked RNA-protein complexes are treated with RNase T1 and the T1-oligonucleotides covalently linked to the proteins are labeled in the 5' terminus using γ-32p-ATP and T4 polynucleotide kinase. The cross-linked proteins can then readily be identified owing to the incorporated 32p label. As examples, proteins associated with polyadenylated mRNA, hnRNA and adenoviral VA RNA were identified. A protein with a molecular weight of approximately 50,000 is found associated with adenovirus-coded VA RNA. This was confirmed by binding assays, in which labeled VAI RNA is incubated with proteins from uninfected and adenovirus infected HeLa cells immobilized on nitrocellulose sheets.
机译:紫外线诱导的RNA蛋白交联用于鉴定与完整细胞中的RNA相互作用的多肽(Wagenmakers等,1980),受蛋白质中标签强度的限制,或在RNase治疗后剩余的残留核苷酸留在蛋白质中RNA蛋白质复合物的含量。在这里,我们报告了一种方法,其中用RNaseT1处理交联的RNA蛋白质复合物,并使用γ- 32-sup> p-在5'末端标记与蛋白质共价连接的T1-寡核苷酸。 ATP和T4多核苷酸激酶。然后可以容易地识别交联的蛋白质,因为掺入的 32/15> p标记。作为实例,鉴定了与聚腺苷酸化mRNA,HNRNA和腺病毒VA RNA相关的蛋白质。发现分子量约为50,000的蛋白质与腺病毒编码的VA RNA相关。通过结合测定来证实,其中标记的Vai RNA与来自未感染的蛋白质和固定在硝酸纤维素片上的腺病毒感染的Hela细胞的蛋白质一起温育。

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