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针对转录中间体单链DNA的大肠杆菌RNA聚合酶抑制剂。1,10-菲咯啉的四面体亚铜螯合物。

Inhibitors of Escherichia coli RNA polymerase specific for the single-stranded DNA of transcription intermediates. Tetrahedral cuprous chelates of 1,10-phenanthrolines.

作者信息

Perrin D M, Hoang V M, Xu Y, Mazumder A, Sigman D S

机构信息

Department of Biological Chemistry, School of Medicine, University of California, Los Angeles 90095-1570, USA.

出版信息

Biochemistry. 1996 Apr 23;35(16):5318-26. doi: 10.1021/bi952197r.

Abstract

Single-stranded DNA of the lacUV-5 promoter formed at the active site of Escherichia coli RNA polymerase during transcription is specifically cleaved by the redox active tetrahedral cuprous chelates of 1,10-phenanthroline and its derivatives. The cleavage sites are observed in the open, initiating, and elongating complexes. Redox-inert, tetrahedral cuprous chelates of neocuproine (2,9-dimethyl-1,10- phenanthroline) and its 5-phenyl and 4-phenyl derivatives protect the template strand of DNA from scission within these steady state intermediates and inhibit transcription. Although these cuprous chelates of neocuproine bind at multiple sites within three distinct enzyme intermediates, the highest affinity site is within the elongation complex. The I50 of 5 microM for the 2:1 5-phenylneocuproine cuprous complex ((5 phi NC)2Cu+) in runoff transcription therefore primarily reflects its intermediate. The neocuproine cuprous chelates are novel transcription inhibitors because they bind to single-stranded DNA sites generated during the course of catalysis by RNA polymerase.

摘要

在转录过程中,在大肠杆菌RNA聚合酶活性位点形成的lacUV - 5启动子单链DNA被1,10 - 菲咯啉及其衍生物的氧化还原活性四面体亚铜螯合物特异性切割。在开放、起始和延伸复合物中观察到切割位点。新铜试剂(2,9 - 二甲基 - 1,10 - 菲咯啉)及其5 - 苯基和4 - 苯基衍生物的氧化还原惰性四面体亚铜螯合物可保护DNA模板链在这些稳态中间体中不被断裂,并抑制转录。尽管这些新铜试剂的亚铜螯合物在三种不同的酶中间体的多个位点结合,但最高亲和力位点在延伸复合物内。因此,在连续转录中,2:1的5 - 苯基新铜试剂亚铜络合物((5 phi NC)2Cu+)的半数抑制浓度为5 microM,这主要反映了其与中间体的结合情况。新铜试剂亚铜螯合物是新型转录抑制剂,因为它们与RNA聚合酶催化过程中产生的单链DNA位点结合。

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