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放线菌素与DNA上的结合位点。

Echinomycin binding sites on DNA.

作者信息

Van Dyke M M, Dervan P B

出版信息

Science. 1984 Sep 14;225(4667):1122-7. doi: 10.1126/science.6089341.

Abstract

The preferred binding sites of echinomycin on DNA can be determined by a method called "footprinting." A 32P end-labeled restriction fragment from pBR322 DNA is protected by binding to echinomycin, and cleaved by a synthetic DNA cleaving reagent, methidiumpropyl--EDTA . Fe(II); the DNA cleavage products are then subjected to high-resolution gel analyses. This method reveals that echinomycin has a binding site size of four base pairs. The strong binding sites for echinomycin contain the central two-base-pair sequence 5'-CG-3'. From an analysis of 15 echinomycin sites on 210 base pairs of DNA, key recognition elements for echinomycin are contained in the sequences (5'-3') ACGT and TCGT (A, adenine; C, cytosine; G, guanine; T, thymine).

摘要

放线菌素对DNA的优先结合位点可通过一种称为“足迹法”的方法来确定。来自pBR322 DNA的32P末端标记的限制片段通过与放线菌素结合而受到保护,并被一种合成DNA切割试剂甲啶丙基-乙二胺四乙酸铁(II)切割;然后对DNA切割产物进行高分辨率凝胶分析。该方法表明,放线菌素的结合位点大小为四个碱基对。放线菌素的强结合位点包含中心两碱基对序列5'-CG-3'。通过对210个碱基对DNA上的15个放线菌素位点进行分析,放线菌素的关键识别元件包含在序列(5'-3')ACGT和TCGT中(A,腺嘌呤;C,胞嘧啶;G,鸟嘌呤;T,胸腺嘧啶)。

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