DNA DISTORTION IN BIS-INTERCALATED COMPLEXES

被引:41
作者
PEEK, ME
LIPSCOMB, LA
BERTRAND, JA
GAO, Q
ROQUES, BP
GARBAYJAUREGUIBERRY, C
WILLIAMS, LD
机构
[1] GEORGIA INST TECHNOL,SCH CHEM & BIOCHEM,ATLANTA,GA 30332
[2] BRISTOL MYERS SQUIBB CO,DEPT ANALYT CHEM,WALLINGFORD,CT 06492
[3] UER SCI PHARMACEUT & BIOL,CNRS,RA 4500,INSERM,U266,DEPT CHIM ORGAN,F-75006 PARIS,FRANCE
关键词
D O I
10.1021/bi00179a002
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 bis-intercalators Flexi-Di and ditercalinium are synthetic dimers that bis-intercalate into DNA and cause cell death in prokaryotes from futile and abortive repair of DNA. Each is composed of two 7H-pyridocarbazole units and a linker. Flexi-Di has a flexible spermine-like linker while ditercalinium has a rigid bis(ethylpiperidinium) linker. This report, describing the 2.5-angstrom X-ray structure of Flexi-Di complexed with [d((Br)CGCG)]2, appears to be the first report of a three-dimensional structure of a DNA complex with a bis-intercalator with a flexible linker. DNA complex formation with a ditercalinium analog having a flexible linker was not anticipated to yield unstacked and bent DNA as was observed in the previously reported ditercalinium.[d(CGCG)]2 complex. Surprisingly, the DNA in the Flexi-Di complex is bent to a degree exceeding that of the ditercalinium complex. A comparison of the DNA complexes of Flexi-Di and ditercalinium has allowed us to propose a mechanism by which these bis-intercalators distort DNA. We propose that this class of bis-intercalators pulls the internal base pairs into the major groove and pushes the external base pairs into the minor groove. The result is a bend toward the minor groove. It appears that hydrogen bonds between the linker and the internal guanines effectively pull the central base pairs of the complex out into the major groove. At the external regions of the complex, stacking interactions between the chromophores and terminal base pairs effectively push the terminal base pairs into the minor groove. The result of this push/pull combination is to bend the DNA.
引用
收藏
页码:3794 / 3800
页数:7
相关论文
共 35 条
[1]  
BRUNGER AT, 1988, XPLOR SOFTWARE
[2]   STEREOCHEMISTRY OF NUCLEIC ACIDS AND THEIR CONSTITUENTS .10. SOLID-STATE BASE-STACKING PATTERNS IN NUCLEIC ACID CONSTITUENTS AND POLYNUCLEOTIDES [J].
BUGG, CE ;
THOMAS, JM ;
RAO, ST ;
SUNDARALINGAM, M .
BIOPOLYMERS, 1971, 10 (01) :175-+
[3]   EFFECTS OF HALOGEN SUBSTITUENTS ON BASE STACKING IN NUCLEIC ACID COMPONENTS - CRYSTAL STRUCTURE OF 8-BROMOGUANOSINE [J].
BUGG, CE ;
THEWALT, U .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1969, 37 (04) :623-&
[4]   GEOMETRY OF THE ANTITUMOR DRUG DITERCALINIUM BISINTERCALATED INTO D(CPGPCPG)2 BY H-1-NMR [J].
DELBARRE, A ;
DELEPIERRE, M ;
GARBAY, C ;
IGOLEN, J ;
LEPECQ, JB ;
ROQUES, BP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (08) :2155-2159
[5]   BISINTERCALATION OF DITERCALINIUM INTO A D[CPGPCPG]2 MINIHELIX - STRUCTURE AND DYNAMICS ASPECTS - A 400-MHZ H-1-NMR STUDY [J].
DELBARRE, A ;
DELEPIERRE, M ;
DESTAINTOT, BL ;
IGOLEN, J ;
ROQUES, BP .
BIOPOLYMERS, 1987, 26 (07) :1001-1033
[6]   CRYSTAL-LATTICE PACKING IS IMPORTANT IN DETERMINING THE BEND OF A DNA DODECAMER CONTAINING AN ADENINE TRACT [J].
DIGABRIELE, AD ;
SANDERSON, MR ;
STEITZ, TA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (06) :1816-1820
[7]   STRUCTURE OF A B-DNA DODECAMER - CONFORMATION AND DYNAMICS .1. [J].
DREW, HR ;
WING, RM ;
TAKANO, T ;
BROKA, C ;
TANAKA, S ;
ITAKURA, K ;
DICKERSON, RE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (04) :2179-2183
[8]   STRUCTURE OF THE PURE-SPERMINE FORM OF Z-DNA (MAGNESIUM FREE) AT 1-A RESOLUTION [J].
EGLI, M ;
WILLIAMS, LD ;
GAO, Q ;
RICH, A .
BIOCHEMISTRY, 1991, 30 (48) :11388-11402
[9]   DRUG-INDUCED DNA-REPAIR - X-RAY STRUCTURE OF A DNA-DITERCALINIUM COMPLEX [J].
GAO, Q ;
WILLIAMS, LD ;
EGLI, M ;
RABINOVICH, D ;
CHEN, SL ;
QUIGLEY, GJ ;
RICH, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (06) :2422-2426
[10]   SYNTHESIS AND BIOLOGICAL-ACTIVITY OF NEW DIMERS IN THE 7H-PYRIDO[4,3-C]CARBAZOLE ANTITUMOR SERIES [J].
GARBAYJAUREGUIBERRY, C ;
BARSI, MC ;
JACQUEMINSABLON, A ;
LEPECQ, JB ;
ROQUES, BP .
JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (01) :72-81