Solution NMR Structure of a Ligand/Hybrid-2-G-Quadruplex Complex Reveals Rearrangements that Affect Ligand Binding

被引:42
作者
Wirmer-Bartoschek, Julia [1 ]
Bendel, Lars Erik [1 ]
Jonker, Hendrik R. A. [1 ]
Gruen, J. Tassilo [1 ]
Papi, Francesco [2 ]
Bazzicalupi, Carla [2 ]
Messori, Luigi [2 ]
Gratteri, Paola [3 ]
Schwalbe, Harald [1 ]
机构
[1] Goethe Univ Frankfurt Main, Ctr Biomol Magnet Resonance BMRZ, Inst Organ Chem & Chem Biol, Max von Laue Str 7, D-60439 Frankfurt, Germany
[2] Univ Firenze, Dipartimento Chim Ugo Schiff, Via Lastruccia 3, I-50019 Sesto Fiorentino, FI, Italy
[3] Univ Firenze, Dipartimento Neurosci, Area Farmaco, Salute Bambino NEUROFARBA,Psicol, Via Ugo Schiff 6, I-50019 Sesto Fiorentino, FI, Italy
基金
欧盟地平线“2020”;
关键词
DNA-ligand complexes; drug design; G-quadruplexes; NMR spectroscopy; structure elucidation; TELOMERIC G-QUADRUPLEX; C-MYC TRANSCRIPTION; FIELD GRADIENTS; K+ SOLUTION; DNA; SPECTROSCOPY; SENSITIVITY; SEQUENCES; POLYMORPHISM; SUPPRESSION;
D O I
10.1002/anie.201702135
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Telomeric G-quadruplexes have recently emerged as drug targets in cancer research. Herein, we present the first NMR structure of a telomeric DNAG-quadruplex that adopts the biologically relevant hybrid-2 conformation in a ligand-bound state. We solved the complex with a metalorganic gold(III) ligand that stabilizes G-quadruplexes. Analysis of the free and bound structures reveals structural changes in the capping region of the G-quadruplex. The ligand is sandwiched between one terminal G-tetrad and a flanking nucleotide. This complex structure involves a major structural rearrangement compared to the free G-quadruplex structure as observed for other G-quadruplexes in different conformations, invalidating simple docking approaches to ligand-G-quadruplex structure determination.
引用
收藏
页码:7102 / 7106
页数:5
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