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博来霉素与DNA的结合:双噻唑环的嵌入

Binding of bleomycin to DNA: intercalation of the bithiazole rings.

作者信息

Povirk L F, Hogan M, Dattagupta N

出版信息

Biochemistry. 1979 Jan 9;18(1):96-101. doi: 10.1021/bi00568a015.

Abstract

At pH 5.5, binding of bleomycin relaxed supercoiled ColE1 DNA without breaking it. Binding of tripeptide S, a fragment of the drug containing the bithiazole rings, also relaxed and then recoiled supercoiled DNA, at pH 5.5 and at pH 8.0, where bleomycin is normally active. The unwinding angle was 12 degrees. Both compounds lengthened linear DNA by 3.1 A per molecule bound, and linear dichroism (303--315 nm) of bleomycin bound to linear DNA oriented in an electric field indicated the presence of a chromophore making an angle of 59--61 degrees with the helix axis. These results strongly suggest that bleomycin binding to DNA involves intercalation of the bithiazole rings. In 0.1 M Na Cl at pH 8, supercoiled ColE1 DNA was broken at a rate 50% greater than relaxed closed circular ColE1 DNA. Since supercoiling increases the affinity of DNA for intercalators, this result suggests that intercalative binding is involved in bleomycin-induced breakage of DNA.

摘要

在pH 5.5时,博来霉素与松弛的超螺旋ColE1 DNA结合而不将其切断。三肽S(该药物含有双噻唑环的一个片段)在pH 5.5以及博来霉素通常具有活性的pH 8.0时,也能使超螺旋DNA松弛然后再卷曲。解旋角度为12度。两种化合物每结合一个分子可使线性DNA延长3.1埃,并且与电场中定向的线性DNA结合的博来霉素的线性二色性(303 - 315纳米)表明存在一个与螺旋轴成59 - 61度角的发色团。这些结果有力地表明博来霉素与DNA的结合涉及双噻唑环的嵌入。在pH 8的0.1 M氯化钠中,超螺旋ColE1 DNA的断裂速率比松弛的闭环ColE1 DNA高50%。由于超螺旋增加了DNA对嵌入剂的亲和力,这一结果表明嵌入结合参与了博来霉素诱导的DNA断裂。

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