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Crosslinking and cleavage of pBR322 DNA photosensitized by 7-methylpyrido[3,4-c]psoralen.

作者信息

Chen X, Kagan J

机构信息

Department of Chemistry, University of Illinois, Chicago 60607-7061.

出版信息

J Photochem Photobiol B. 1994 Apr;23(1):27-33. doi: 10.1016/1011-1344(93)06979-d.

DOI:10.1016/1011-1344(93)06979-d
PMID:8021747
Abstract

7-Methylpyrido[3,4-c]psoralen (7-MPP) had been designed to be a monofunctional sensitizer in which the pyrone double bond, being engaged in a pyridine ring, would be incapable of participating in the formation of a cyclobutane ring with a DNA component. However, one example of photosensitization of thymine-thymine dimer formation in DNA by 7-MPP had been reported. This paper proves that 7-MPP can sensitize interstrand crosslinks in pBR322 DNA. It also proves that 7-MPP photosensitizes double strand cleavage reactions in the DNA with an unusually large degree of site selectivity.

摘要

相似文献

1
Crosslinking and cleavage of pBR322 DNA photosensitized by 7-methylpyrido[3,4-c]psoralen.
J Photochem Photobiol B. 1994 Apr;23(1):27-33. doi: 10.1016/1011-1344(93)06979-d.
2
Sites of preferred interaction between double-stranded pBR322 DNA and 7-methylpyrido[3,4-c]psoralen.双链pBR322 DNA与7-甲基吡啶并[3,4-c]补骨脂素之间优先相互作用的位点
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