PHOTOSENSITIZED CROSS-LINKING AND CLEAVAGE OF PBR322 AND M13 DNA - COMPARISON OF 4,4',6-TRIMETHYLANGELICIN AND 3-CARBETHOXYPSORALEN

被引:31
作者
CHEN, X
KAGAN, J
MIOLO, G
ACQUA, FD
AVERBECK, D
BISAGNI, E
机构
[1] UNIV ILLINOIS CHICAGO, DEPT CHEM, M-C 111, 845 W TAYLOR ST, CHICAGO, IL 60607 USA
[2] INST CURIE, F-75231 PARIS, FRANCE
[3] INST CURIE, SYNTH ORGAN LAB, CNRS, UA 533, F-91405 ORSAY, FRANCE
[4] UNIV PADUA, DIPARTIMENTO SCI FARMACEUT, I-35131 PADUA, ITALY
关键词
DENATURING GEL; DNA CROSS-LINKING; DNA CLEAVAGE; ELECTROPHORESIS; LINEARIZED DNA; M13; DNA; PBR322; PUVA THERAPY;
D O I
10.1016/1011-1344(93)06953-Z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The furocoumarins 3-carbethoxypsoralen (3-CP) and 4,4',6-trimethylangelicin (TMA) were generally believed to be incapable of cross-linking DNA upon irradiation with ultraviolet light. Denaturation of photosensitized pBR322 DNA, either supercoiled or previously linearized with a restriction enzyme, proved that 3-CP was indeed monofunctional, but that TMA produced cross-links. Identical conclusions were reached with double stranded M13 DNA which had been linearized with EcoR 1. Both sensitizers also induced partial DNA cleavage. In contrast to 3-CP, photosensitization with TMA made the DNA resistant to enzymatic cleavage.
引用
收藏
页码:51 / 57
页数:7
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