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重组CTF/NF-1转录因子的过表达及结合活性的重新激活。

Overexpression and reactivation of binding activity of the recombinant CTF/NF-1 transcription factor.

作者信息

Amemiya K, Durham L, Major E O

机构信息

IGEN Inc., Rockville, Maryland 20852.

出版信息

Protein Expr Purif. 1994 Feb;5(1):57-64. doi: 10.1006/prep.1994.1008.

Abstract

The transcription factor CTF/NF-1 is a multifunctional cellular protein which participates in the expression of host and viral genes and in the replication of viral DNA. A procedure was developed to obtain recombinant CTF/NF-1 protein in order to help identify the binding sites of CTF/NF-1 protein in the regulatory region of viral sequences. Cloning and expression of the CTF/NF-1 gene downstream from a T7 RNA polymerase promoter resulted in an insoluble protein produced in Escherichia coli. Specific binding by the recombinant CTF/NF-1 protein to its cognate recognition site was obtained only after a denaturation and renaturation procedure. No special chromatography steps were required to obtain a rCTF/NF-1 preparation which could be used for our binding studies. Specific binding was detected with an NF-1 oligonucleotide and with viral DNA templates. Binding to the viral DNA sequences was identical to that previously published with biochemically purified cellular CTF/NF-1 protein.

摘要

转录因子CTF/NF-1是一种多功能细胞蛋白,它参与宿主基因和病毒基因的表达以及病毒DNA的复制。为了帮助确定CTF/NF-1蛋白在病毒序列调控区域的结合位点,人们开发了一种获取重组CTF/NF-1蛋白的方法。将CTF/NF-1基因克隆并表达于T7 RNA聚合酶启动子下游,结果在大肠杆菌中产生了一种不溶性蛋白。只有经过变性和复性程序后,重组CTF/NF-1蛋白才能与它的同源识别位点发生特异性结合。获得用于我们结合研究的rCTF/NF-1制剂不需要特殊的色谱步骤。用NF-1寡核苷酸和病毒DNA模板检测到了特异性结合。与病毒DNA序列的结合与先前发表的用生化方法纯化的细胞CTF/NF-1蛋白的结合情况相同。

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