Enantiospecific recognition of DNA sequences by a proflavine Troger base

被引:65
作者
Bailly, C
Laine, W
Demeunynck, M
Lhomme, J
机构
[1] Ctr Oscar Lambret, Inst Rech Canc, INSERM, U524, F-59045 Lille, France
[2] Ctr Oscar Lambret, Inst Rech Canc, Pharmacol Lab, F-59045 Lille, France
[3] Univ Grenoble 1, LEDSS, CNRS, UMR 5616, F-38041 Grenoble, France
关键词
DNA binding; sequence recognition; DNase I footprinting; enantiospecificity;
D O I
10.1006/bbrc.2000.2997
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 DNA interaction of a chiral Troger base derived from proflavine was investigated by DNA melting temperature measurements and complementary biochemical assays. DNase I footprinting experiments demonstrate that the binding of the proflavine-based Troger base is both enantio- and sequence-specific. The (+)-isomer poorly interacts with DNA in a non-sequence-selective fashion. In sharp contrast, the corresponding (-)-isomer recognizes preferentially certain DNA sequences containing both A . T and G . C base pairs, such as the motifs 5'-GTT . AAC and 5'-ATGA . TCAT. This is the first experimental demonstration that acridine-type Troger bases can be used for enantiospecific recognition of DNA sequences, (C) 2000 Academic Press.
引用
收藏
页码:681 / 685
页数:5
相关论文
共 37 条
[1]   CHEMISTRY OF SYNTHETIC RECEPTORS AND FUNCTIONAL-GROUP ARRAYS .10. ORDERLY FUNCTIONAL-GROUP DYADS - RECOGNITION OF BIOTIN AND ADENINE-DERIVATIVES BY A NEW SYNTHETIC HOST [J].
ADRIAN, JC ;
WILCOX, CS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (20) :8055-8057
[2]   CHEMISTRY OF SYNTHETIC RECEPTORS AND FUNCTIONAL-GROUP ARRAYS .15. EFFECTS OF ADDED WATER ON THERMODYNAMIC ASPECTS OF HYDROGEN-BOND-BASED MOLECULAR RECOGNITION IN CHLOROFORM [J].
ADRIAN, JC ;
WILCOX, CS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (02) :678-680
[3]   THE CHEMISTRY OF SYNTHETIC RECEPTORS AND FUNCTIONAL GROUP ARRAYS .19. GENERAL EFFECTS OF BINDING-SITE WATER EXCLUSION ON HYDROGEN-BOND BASED MOLECULAR RECOGNITION SYSTEMS - A CLOSED BINDING-SITE IS LESS AFFECTED BY ENVIRONMENTAL-CHANGES THAN AN OPEN SITE [J].
ADRIAN, JC ;
WILCOX, CS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (04) :1398-1403
[4]  
BAG BG, 1995, CURR SCI INDIA, V68, P279
[5]   COMPARISON OF DIFFERENT FOOTPRINTING METHODOLOGIES FOR DETECTING BINDING-SITES FOR A SMALL LIGAND ON DNA [J].
BAILLY, C ;
WARING, MJ .
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 1995, 12 (04) :869-898
[6]   Sequence-selective intercalation of antitumour bis-naphthalimides into DNA - Evidence for an approach via the major groove [J].
Bailly, C ;
Brana, M ;
Waring, MJ .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 240 (01) :195-208
[7]   BINDING MODES AND BASE SPECIFICITY OF TRIS(PHENANTHROLINE)RUTHENIUM(II) ENANTIOMERS WITH NUCLEIC-ACIDS - TUNING THE STEREOSELECTIVITY [J].
BARTON, JK ;
GOLDBERG, JM ;
KUMAR, CV ;
TURRO, NJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (08) :2081-2088
[8]  
CHOW CS, 1992, METHOD ENZYMOL, V212, P219
[9]   Electric linear dichroism as a new tool to study sequence preference in drug binding to DNA [J].
Colson, P ;
Bailly, C ;
Houssier, C .
BIOPHYSICAL CHEMISTRY, 1996, 58 (1-2) :125-140
[10]   ENANTIOSELECTIVE RECOGNITION OF HISTIDINE AND LYSINE ESTERS BY PORPHYRIN CHIRAL CLEFTS AND DETECTION OF AMINO-ACID CONFORMATIONS IN THE BOUND-STATE [J].
CROSSLEY, MJ ;
MACKAY, LG ;
TRY, AC .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1995, (18) :1925-1927