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DNA嵌入剂对限制性内切酶切割的选择性抑制作用。

Selective inhibition of restriction endonuclease cleavage by DNA intercalators.

作者信息

Soslau G, Pirollo K

出版信息

Biochem Biophys Res Commun. 1983 Sep 15;115(2):484-91. doi: 10.1016/s0006-291x(83)80170-3.

Abstract

The preferred dye binding sites and the microenvironment of known nucleotide sequences within mitochondrial and plasmid pBR322 DNA was probed in a gross fashion with restriction endonucleases. The intercalating dyes, ethidium bromide and propidium iodide, do not inhibit a given restriction endonuclease equally at all of the restriction sites within a DNA molecule. The selective inhibition may be explained, in part, by the potential B to Z conformation transition of DNA flanking the restriction site and by preferred dye binding sites. Propidium iodide was found to be a more potent inhibitor than ethidium bromide and the inhibition is independent of the type of cut made by the enzyme.

摘要

利用限制性内切酶大致探测了线粒体和质粒pBR322 DNA内已知核苷酸序列的优选染料结合位点和微环境。嵌入染料溴化乙锭和碘化丙啶,在DNA分子内的所有限制性位点处,对给定的限制性内切酶的抑制作用并不相同。这种选择性抑制部分可通过限制性位点侧翼DNA潜在的B到Z构象转变以及优选的染料结合位点来解释。发现碘化丙啶是比溴化乙锭更有效的抑制剂,且这种抑制与酶所产生的切割类型无关。

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