Looped out and perpendicular: Deformation of Watson-Crick base pair associated with actinomycin D binding

被引:29
|
作者
Chou, SH [1 ]
Chin, KH
Chen, FM
机构
[1] Natl Chung Hsing Univ, Inst Biochem, Taichung 40227, Taiwan
[2] Tennessee State Univ, Dept Chem, Nashville, TN 37209 USA
关键词
D O I
10.1073/pnas.102580399
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Many anticancer drugs interact directly with DNA to exert their biological functions. To date, all noncovalent, intercalating drugs interact with DNA exclusively by inserting their chromophores into base steps to form elongated and unwound duplex structures without disrupting the flanking base pairs. By using actinomycin D (ActD)-5'-GXC/CYG-5' complexes as examples, we have found a rather unusual interaction mode for the intercalated drug; the central Watson-Crick X/Y base pairs are looped out and displaced by the ActD chromophore. The looped-out bases are not disordered but interact perpendicularly with the base/chromophore and form specific H bonds with DNA. Such a complex structure provides intriguing insights into how ligand interacts with DNA and enlarges the repertoires for sequence-specific DNA recognition.
引用
收藏
页码:6625 / 6630
页数:6
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