Discovery of G-quadruplex stabilizing ligands through direct ELISA of a one-bead-one-compound library.

We describe the identification of small-molecule G-quadruplex ligands using a direct ELISA screen of a one-bead-one-compound library of unnatural polyamides displayed on a branched linker with a biotin tag. This general purpose parallel screen for small molecule-oligonucleotide interactions was validated by surface plasmon resonance and ELISA of resynthesized compounds. Linear polyamides displayed similar rankings in their affinity for quadruplex as their branched counterparts. Quadruplex affinity as judged by these surface based techniques was a useful predictor of the ability of the ligands to stabilize the quadruplex to thermal unfolding in solution.

[1]  Á. Furka,et al.  General method for rapid synthesis of multicomponent peptide mixtures. , 2009, International journal of peptide and protein research.

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

[3]  Dinshaw J. Patel,et al.  Structure of the human telomere in K+ solution: an intramolecular (3 + 1) G-quadruplex scaffold. , 2006, Journal of the American Chemical Society.

[4]  Stephen Neidle,et al.  A conserved quadruplex motif located in a transcription activation site of the human c-kit oncogene. , 2006, Biochemistry.

[5]  Yan Xu,et al.  Formation of the G-quadruplex and i-motif structures in retinoblastoma susceptibility genes (Rb) , 2006, Nucleic acids research.

[6]  Stephen Neidle,et al.  Putative DNA quadruplex formation within the human c-kit oncogene. , 2005, Journal of the American Chemical Society.

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

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

[9]  J. Riou G-quadruplex interacting agents targeting the telomeric G-overhang are more than simple telomerase inhibitors. , 2004, Current medicinal chemistry. Anti-cancer agents.

[10]  W. Hahn,et al.  Telomerase Maintains Telomere Structure in Normal Human Cells , 2003, Cell.

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

[12]  G. Parkinson,et al.  The structure of telomeric DNA. , 2003, Current opinion in structural biology.

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

[14]  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.

[15]  Stephen Neidle,et al.  Crystal structure of parallel quadruplexes from human telomeric DNA , 2002, Nature.

[16]  M. Searle,et al.  Recognition and stabilization of quadruplex DNA by a potent new telomerase inhibitor: NMR studies of the 2:1 complex of a pentacyclic methylacridinium cation with d(TTAGGGT)4 , 2001 .

[17]  Stephen Neidle,et al.  Structure-based design of selective and potent G quadruplex-mediated telomerase inhibitors , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[18]  P. Dervan,et al.  Fmoc solid phase synthesis of polyamides containing pyrrole and imidazole amino acids. , 2001, Organic letters.

[19]  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.

[20]  C. Carlson,et al.  Solid-phase synthesis of acridine-peptide conjugates and their analysis by tandem mass spectrometry. , 2000, Organic letters.

[21]  P. Pečinka,et al.  DNA tetraplex formation in the control region of c-myc. , 1998, Nucleic acids research.

[22]  C B Harley,et al.  Specific association of human telomerase activity with immortal cells and cancer. , 1994, Science.

[23]  D. Patel,et al.  Solution structure of the human telomeric repeat d[AG3(T2AG3)3] G-tetraplex. , 1993, Structure.

[24]  D. Patel,et al.  Guanine residues in d(T2AG3) and d(T2G4) form parallel-stranded potassium cation stabilized G-quadruplexes with anti glycosidic torsion angles in solution. , 1992, Biochemistry.

[25]  S. Blondelle,et al.  The use of synthetic peptide combinatorial libraries for the identification of bioactive peptides. , 1992, BioTechniques.

[26]  K. Lam,et al.  A new type of synthetic peptide library for identifying ligand-binding activity , 1992, Nature.

[27]  David M. Prescott,et al.  Inhibition of telomerase by G-quartet DMA structures , 1991, Nature.

[28]  Kathryn S. Prickett,et al.  A Short Polypeptide Marker Sequence Useful for Recombinant Protein Identification and Purification , 1988, Bio/Technology.

[29]  J. Tam,et al.  Synthetic peptide vaccine design: synthesis and properties of a high-density multiple antigenic peptide system. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[30]  W. D. Wilson,et al.  Surface plasmon resonance biosensor analysis of RNA-small molecule interactions. , 2001, Methods in enzymology.

[31]  K. Lam Enzyme-linked colorimetric screening of a one-bead one-compound combinatorial library. , 1998, Methods in molecular biology.