PORPHYRIN INTERCALATION AND NONSPECIFIC EDGE ON OUTSIDE BINDING TO NATURAL DNA

被引:21
作者
FENG, Y
PILBROW, JR
机构
[1] Department of Physics, Monash University, Clayton
关键词
Base sequence specificity; DNA binding; Ionic strength dependence; Modified matrix method; Theoretical model; Two-mode binding;
D O I
10.1016/0301-4622(90)85015-X
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
A theoretical two-mode binding model for porphyrin binding to natural DNA is presented. One of the binding modes is assumed to be base sequence specific with binding sites n base-pairs long. The other binding mode has binding sites which consist of only one base-pair and can involve cooperativity. The model fits satisfactorily to data for H2TMPyP-4, Cu(II)TMPyP-3 and Cu(II)TMPyP-4 binding to calf thymus DNA in both a high (μ {reversed tilde equals} 1.0 M) and a low (μ {reversed tilde equals} 0.2 M) ionic strength buffer. The results show that the fraction of porphyrin bound in the non-specific mode reaches a maximum at certain input DNA to porphyrin concentration ratios. The value of this maximum decreased, and its position shifted to higher DNA to porphyrin concentration ratios for binding in the high ionic strength buffer. The value of the cooperativity parameter obtained through the fitting process suggests that the non-specific binding is positively cooperative. The results are compared with the data analysed using other techniques. © 1990.
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页码:117 / 131
页数:15
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