Template-assembled synthetic G-quadruplex (TASQ): a useful system for investigating the interactions of ligands with constrained quadruplex topologies.

A new biomolecular device for investigating the interactions of ligands with constrained DNA quadruplex topologies, using surface plasmon resonance (SPR), is reported. Biomolecular systems containing an intermolecular-like G-quadruplex motif 1 (parallel G-quadruplex conformation), an intramolecular G-quadruplex 2, and a duplex DNA 3 have been designed and developed. The method is based on the concept of template-assembled synthetic G-quadruplex (TASQ), whereby quadruplex DNA structures are assembled on a template that allows precise control of the parallel G-quadruplex conformation. Various known G-quadruplex ligands have been used to investigate the affinities of ligands for intermolecular 1 and intramolecular 2 DNA quadruplexes. As anticipated, ligands displaying a pi-stacking binding mode showed a higher binding affinity for intermolecular-like G-quadruplexes 1, whereas ligands with other binding modes (groove and/or loop binding) showed no significant difference in their binding affinities for the two quadruplexes 1 or 2. In addition, the present method has also provided information about the selectivity of ligands for G-quadruplex DNA over the duplex DNA. A numerical parameter, termed the G-quadruplex binding mode index (G4-BMI), has been introduced to express the difference in the affinities of ligands for intermolecular G-quadruplex 1 against intramolecular G-quadruplex 2. The G-quadruplex binding mode index (G4-BMI) of a ligand is defined as follows: G4-BMI=K(D)(intra)/K(D)(inter), where K(D)(intra) is the dissociation constant for intramolecular G-quadruplex 2 and K(D)(inter) is the dissociation constant for intermolecular G-quadruplex 1. In summary, the present work has demonstrated that the use of parallel-constrained quadruplex topology provides more precise information about the binding modes of ligands.

[1]  Stephen Neidle,et al.  Human telomeric G‐quadruplex: The current status of telomeric G‐quadruplexes as therapeutic targets in human cancer , 2010, The FEBS journal.

[2]  J. Karlseder,et al.  Telomeric armor: the layers of end protection , 2009, Journal of Cell Science.

[3]  J. Sherman,et al.  Cation-complexation behavior of template-assembled synthetic G-quartets. , 2009, The Journal of organic chemistry.

[4]  Stephen Neidle,et al.  The structures of quadruplex nucleic acids and their drug complexes. , 2009, Current opinion in structural biology.

[5]  S. Balasubramanian,et al.  G-quadruplex nucleic acids as therapeutic targets. , 2009, Current opinion in chemical biology.

[6]  G. Piccialli,et al.  Synthesis of quadruplex‐forming tetra‐end‐linked oligonucleotides: Effects of the linker size on quadruplex topology and stability , 2009, Biopolymers.

[7]  M. Franceschin G‐Quadruplex DNA Structures and Organic Chemistry: More than One Connection , 2009 .

[8]  H. Ihmels,et al.  Diazonia- and tetraazoniapolycyclic cations as motif for quadruplex-DNA ligands. , 2009, Chemical communications.

[9]  A. Canals,et al.  DNA-binding drugs caught in action: the latest 3D pictures of drug-DNA complexes. , 2009, Dalton transactions.

[10]  Stephen Neidle,et al.  Recognition and discrimination of DNA quadruplexes by acridine-peptide conjugates. , 2009, Organic & biomolecular chemistry.

[11]  P. Labbé,et al.  A Novel Conformationally Constrained Parallel G Quadruplex , 2008, Chembiochem : a European journal of chemical biology.

[12]  R. Vilar,et al.  Stabilisation of G-quadruplex DNA by small molecules. , 2008, Current topics in medicinal chemistry.

[13]  E. De Pauw,et al.  Ligand binding to tetra-end-linked (TGGGGT)4 G-quadruplexes: an electrospray mass spectroscopy study. , 2008, Nucleic Acids Symposium Series.

[14]  Danzhou Yang,et al.  Polymorphism of human telomeric quadruplex structures. , 2008, Biochimie.

[15]  N. Smargiasso,et al.  Ligands playing musical chairs with G-quadruplex DNA: a rapid and simple displacement assay for identifying selective G-quadruplex binders. , 2008, Biochimie.

[16]  Laurence H. Hurley,et al.  Structures, folding patterns, and functions of intramolecular DNA G-quadruplexes found in eukaryotic promoter regions. , 2008, Biochimie.

[17]  B. Pagano,et al.  Targeting DNA quadruplexes with distamycin A and its derivatives: an ITC and NMR study. , 2008, Biochimie.

[18]  P. Bolton,et al.  Mix and measure fluorescence screening for selective quadruplex binders , 2008, Nucleic acids research.

[19]  E. De Pauw,et al.  Electrospray mass spectrometry to study drug-nucleic acids interactions. , 2008, Biochimie.

[20]  J. Sherman,et al.  Template-assembled synthetic G-quartets (TASQs). , 2008, Angewandte Chemie.

[21]  M. Teulade‐Fichou,et al.  A hitchhiker's guide to G-quadruplex ligands. , 2008, Organic & biomolecular chemistry.

[22]  Giuseppe Bifulco,et al.  Structural and thermodynamic studies of the interaction of distamycin A with the parallel quadruplex structure [d(TGGGGT)]4. , 2007, Journal of the American Chemical Society.

[23]  J. Chaires,et al.  Use of competition dialysis in the discovery of G-quadruplex selective ligands. , 2007, Methods.

[24]  J. Redman Surface plasmon resonance for probing quadruplex folding and interactions with proteins and small molecules. , 2007, Methods.

[25]  J. Leroy,et al.  The formation pathway of tetramolecular G-quadruplexes , 2007, Nucleic acids research.

[26]  K. Shin‐ya,et al.  Reevaluation of telomerase inhibition by quadruplex ligands and their mechanisms of action , 2007, Proceedings of the National Academy of Sciences.

[27]  M. Graham,et al.  Telomerase recognizes G-quadruplex and linear DNA as distinct substrates. , 2007, Biochemistry.

[28]  L. Kèlland,et al.  Targeting the Limitless Replicative Potential of Cancer: The Telomerase/Telomere Pathway , 2007, Clinical Cancer Research.

[29]  L. Hurley,et al.  Formation of pseudosymmetrical G-quadruplex and i-motif structures in the proximal promoter region of the RET oncogene. , 2007, Journal of the American Chemical Society.

[30]  J. Chaires,et al.  Competition dialysis: a method for the study of structural selective nucleic acid binding. , 2007, Methods.

[31]  Markus Kaiser,et al.  Fluorescence-based melting assays for studying quadruplex ligands. , 2007, Methods.

[32]  J. Mergny,et al.  G‐Quadruplex Recognition by Quinacridines: a SAR, NMR, and Biological Study , 2007, ChemMedChem.

[33]  J. Mergny,et al.  Quadruplex ligands may act as molecular chaperones for tetramolecular quadruplex formation , 2007, Nucleic acids research.

[34]  S. Neidle,et al.  Structure-specific recognition of quadruplex DNA by organic cations: influence of shape, substituents and charge. , 2007, Biophysical chemistry.

[35]  G. Parkinson,et al.  Structural basis for binding of porphyrin to human telomeres. , 2007, Biochemistry.

[36]  T. Bryan,et al.  Physiological relevance of telomeric G‐quadruplex formation: a potential drug target , 2007, BioEssays : news and reviews in molecular, cellular and developmental biology.

[37]  Shankar Balasubramanian,et al.  G-quadruplexes in promoters throughout the human genome , 2006, Nucleic acids research.

[38]  N. Maizels,et al.  Dynamic roles for G4 DNA in the biology of eukaryotic cells , 2006, Nature Structural &Molecular Biology.

[39]  Sarah W. Burge,et al.  Quadruplex DNA: sequence, topology and structure , 2006, Nucleic acids research.

[40]  M. Teulade‐Fichou,et al.  Development of a fluorescent intercalator displacement assay (G4-FID) for establishing quadruplex-DNA affinity and selectivity of putative ligands. , 2006, Bioorganic & medicinal chemistry letters.

[41]  Stephen Neidle,et al.  Synthesis of distamycin A polyamides targeting G-quadruplex DNA. , 2006, Organic & biomolecular chemistry.

[42]  Ping Wang,et al.  A Phenol Quaternary Ammonium Porphyrin as a Potent Telomerase Inhibitor by Selective Interaction with Quadruplex DNA , 2006, Chembiochem : a European journal of chemical biology.

[43]  G. Piccialli,et al.  Synthesis and characterization of monomolecular DNA G-quadruplexes formed by tetra-end-linked oligonucleotides. , 2006, Bioconjugate chemistry.

[44]  T. Bryan,et al.  Extension of G‐quadruplex DNA by ciliate telomerase , 2006, The EMBO journal.

[45]  Laurence H. Hurley,et al.  Facilitation of a structural transition in the polypurine/polypyrimidine tract within the proximal promoter region of the human VEGF gene by the presence of potassium and G-quadruplex-interactive agents , 2005, Nucleic acids research.

[46]  Jean-Louis Mergny,et al.  Affinity and selectivity of G4 ligands measured by FRET. , 2005, Nucleic acids symposium series.

[47]  A. Phan,et al.  Small-molecule interaction with a five-guanine-tract G-quadruplex structure from the human MYC promoter , 2005, Nature chemical biology.

[48]  W. Wilson,et al.  Telomestatin and diseleno sapphyrin bind selectively to two different forms of the human telomeric G-quadruplex structure. , 2005, Journal of the American Chemical Society.

[49]  S. Neidle,et al.  Highly prevalent putative quadruplex sequence motifs in human DNA , 2005, Nucleic acids research.

[50]  Shankar Balasubramanian,et al.  Prevalence of quadruplexes in the human genome , 2005, Nucleic acids research.

[51]  Jean-Louis Mergny,et al.  Kinetics of tetramolecular quadruplexes , 2005, Nucleic acids research.

[52]  M. Blasco,et al.  Porphyrin Derivatives for Telomere Binding and Telomerase Inhibition , 2005, Chembiochem : a European journal of chemical biology.

[53]  S. Balasubramanian,et al.  Tetrapeptides induce selective recognition for G-quadruplexes when conjugated to a DNA-binding platform. , 2004, Organic & biomolecular chemistry.

[54]  L. Hurley,et al.  The different biological effects of telomestatin and TMPyP4 can be attributed to their selectivity for interaction with intramolecular or intermolecular G-quadruplex structures. , 2003, Cancer research.

[55]  N. Maizels,et al.  Specific interactions of distamycin with G-quadruplex DNA. , 2003, Nucleic acids research.

[56]  S. Balasubramanian,et al.  G-quadruplex-specific peptide-hemicyanine ligands by partial combinatorial selection. , 2003, Journal of the American Chemical Society.

[57]  Jean-Louis Mergny,et al.  Selective recognition of G-qQuadruplex telomeric DNA by a bis(quinacridine) macrocycle. , 2003, Journal of the American Chemical Society.

[58]  D. Bearss,et al.  Direct evidence for a G-quadruplex in a promoter region and its targeting with a small molecule to repress c-MYC transcription , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[59]  Laurence H. Hurley,et al.  DNA and its associated processes as targets for cancer therapy , 2002, Nature Reviews Cancer.

[60]  R. Wheelhouse,et al.  Quadruplex-interactive agents as telomerase inhibitors: synthesis of porphyrins and structure-activity relationship for the inhibition of telomerase. , 2001, Journal of medicinal chemistry.

[61]  J. Mergny,et al.  Telomerase inhibitors based on quadruplex ligands selected by a fluorescence assay , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[62]  W D Wilson,et al.  Specific molecular recognition of mixed nucleic acid sequences: an aromatic dication that binds in the DNA minor groove as a dimer. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[63]  J. Chaires,et al.  Sequence and structural selectivity of nucleic acid binding ligands. , 1999, Biochemistry.

[64]  R. Wheelhouse,et al.  Interactions of TMPyP4 and TMPyP2 with Quadruplex DNA. Structural Basis for the Differential Effects on Telomerase Inhibition , 1999 .

[65]  E. Raymond,et al.  Effects of cationic porphyrins as G-quadruplex interactive agents in human tumor cells. , 1999, Cancer research.

[66]  R. Wheelhouse,et al.  Cationic Porphyrins as Telomerase Inhibitors: the Interaction of Tetra-(N-methyl-4-pyridyl)porphine with Quadruplex DNA , 1998 .

[67]  J. Lehn,et al.  Cyclobisintercaland Macrocycles: Synthesis and Physicochemical Properties of Macrocyclic Polyamines Containing Two Crescent-Shaped Dibenzophenanthroline Subunits , 1997 .

[68]  I. Kuntz,et al.  Spectroscopic recognition of guanine dimeric hairpin quadruplexes by a carbocyanine dye. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[69]  Dipankar Sen,et al.  A sodium-potassium switch in the formation of four-stranded G4-DNA , 1990, Nature.

[70]  W. Gilbert,et al.  Formation of parallel four-stranded complexes by guanine-rich motifs in DNA and its implications for meiosis , 1988, Nature.

[71]  Jean-Louis Mergny,et al.  Targeting telomeres and telomerase. , 2008, Biochimie.

[72]  G. Bifulco,et al.  Differential-frequency saturation transfer difference NMR spectroscopy allows the detection of different ligand-DNA binding modes. , 2005, Angewandte Chemie.

[73]  J. Chaires,et al.  Preferential Binding of 3,3‘-Diethyloxadicarbocyanine to Triplex DNA , 2000 .