Structure-specific recognition of quadruplex DNA by organic cations: Influence of shape, substituents and charge

被引:182
作者
White, Elizabeth W.
Tanious, Farial
Ismail, Mohamed A.
Reszka, Anthony P.
Neidle, Stephen
Boykin, David W.
Wilson, W. David [1 ]
机构
[1] Georgia State Univ, Dept Chem, Atlanta, GA 30303 USA
[2] Canc Res UK, Biomol Struct Grp, London WC1N 1AX, England
[3] Univ London, Sch Pharm, London WC1N 1AX, England
关键词
synthetic cations; telomere; DNA-quadruplex binding; G-tetrad; BIAcore; ITC;
D O I
10.1016/j.bpc.2006.06.006
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
Combining structure-specific recognition of nucleic acids with limited sequence reading is a promising method to reduce the size of the recognition unit required to achieve the necessary selectivity and binding affinity to control function. It has been demonstrated recently that G-quadruplex DNA structures can be targeted by organic cations in a structure-specific manner. Structural targets of quadruplexes include the planar end surfaces of the G-tetrad stacked columns and four grooves. These provide different geometries and functional groups relative to duplex DNA. We have used surface plasmon resonance and isothermal titration calorimetry to show that binding affinity and selectivity of a series of quadruplex end-stacking molecules to human telomeric DNA are sensitive to compound shape as well as substituent type and position. ITC results indicate that binding is largely enthalpy driven. Circular dichroism was also used to identify a group of structurally related compounds that selectively target quadruplex grooves. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:140 / 153
页数:14
相关论文
共 92 条
[71]   Telomeres and telomerases as drug targets [J].
Rezler, EM ;
Bearss, DJ ;
Hurley, LH .
CURRENT OPINION IN PHARMACOLOGY, 2002, 2 (04) :415-423
[72]  
Rodger A., 1997, Circular Dichroism and Linear Dichroism
[73]   Selective interaction of ethidium derivatives with quadruplexes: An equilibrium dialysis and electrospray ionization mass spectrometry analysis [J].
Rosu, F ;
De Pauw, E ;
Guittat, L ;
Alberti, P ;
Lacroix, L ;
Mailliet, P ;
Riou, JF ;
Mergny, JL .
BIOCHEMISTRY, 2003, 42 (35) :10361-10371
[74]   Telomerase inhibition as cancer therapy [J].
Saretzki, G .
CANCER LETTERS, 2003, 194 (02) :209-219
[75]   Synthesis, biophysical and biological evaluation of 3,6-bis-amidoacridines with extended 9-anilino substituents as potent G-quadruplex-binding telomerase inhibitors [J].
Schultes, CM ;
Guyen, W ;
Cuesta, J ;
Neidle, S .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2004, 14 (16) :4347-4351
[76]   Design and synthesis of an expanded porphyrin that has selectivity for the c-MYC G-quadruplex structure [J].
Seenisamy, J ;
Bashyam, S ;
Gokhale, V ;
Vankayalapati, H ;
Sun, D ;
Siddiqui-Jain, A ;
Streiner, N ;
Shin-ya, K ;
White, E ;
Wilson, WD ;
Hurley, LH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (09) :2944-2959
[77]   FORMATION OF PARALLEL 4-STRANDED COMPLEXES BY GUANINE-RICH MOTIFS IN DNA AND ITS IMPLICATIONS FOR MEIOSIS [J].
SEN, D ;
GILBERT, W .
NATURE, 1988, 334 (6180) :364-366
[78]   THE STRUCTURE AND REPLICATION OF KINETOPLAST DNA [J].
SHAPIRO, TA ;
ENGLUND, PT .
ANNUAL REVIEW OF MICROBIOLOGY, 1995, 49 :117-143
[79]   Novel antitumor and neuroprotective substances discovered by characteristic screenings based on specific molecular targets [J].
Shin-ya, K .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2005, 69 (05) :867-872
[80]   The structure and replication of kinetoplast DNA [J].
Shlomai, J .
CURRENT MOLECULAR MEDICINE, 2004, 4 (06) :623-647