Binding of actinomycin D to single-stranded DNA

被引:10
作者
JaresErijman, EA
Klement, R
Machinek, R
Wadkins, RM
Kankia, BI
Marky, LA
Jovin, TM
机构
[1] MAX PLANCK INST BIOPHYS CHEM,DEPT MOL BIOL,D-37018 GOTTINGEN,GERMANY
[2] UNIV GOTTINGEN,INST ORGAN CHEM,D-3400 GOTTINGEN,GERMANY
[3] NYU,DEPT CHEM,NEW YORK,NY 10003
来源
NUCLEOSIDES & NUCLEOTIDES | 1997年 / 16卷 / 5-6期
关键词
D O I
10.1080/07328319708002931
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 sequence specificity and structural aspects of the mode of interaction of the antitumor drug actinomycin D (AMD) with single-stranded DNA were studied by fluorescence, absorption and NMR spectroscopy, calorimetry, ultrasonic velocity and density measurements, and molecular modeling. The binding is length and sequence dependent, with the tetranucleotide motif TAGT showing the highest affinity. A ''hemi-intercalation'' model for the interaction is proposed.
引用
收藏
页码:661 / 667
页数:7
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