We propose to develop a fundamentally new approach to nucleic acid targeting of DNA duplexes. In the proposed recognition complexes, the targeting strand of DNA inserts itself between the two Watson-Crick faces of the duplex to result in a new type of DNA triplex. These triplexes are termed Janus Wedge triplexes after the Roman god Janus. The targeting Janus Wedge (Jw) residue in the Janus Wedge helix contains two hydrogen bonding faces such that after insertion into the DNA duplex, the Janus Wedge residue is hydrogen bonded to both Watson-Crick faces of the target base pair. The final three-stranded complex contains significantly more interstrand hydrogen bonds than does the target Watson-Crick DNA duplex. We will examine both pyrimidine-like and purine-like analogues for the Janus Wedge residues. Initial studies will focus on the nature of the Janus Wedge triplex - those formed without competing Watson-Crick interactions. Subsequently we will focus on strand invasion processes that will be necessary to permit the targeting of duplex DNA. In this respect, the peptide nucleic acid (PNA) oligomers, other oligomers with neutral backbones, selected tethered ligands, and the process of DNA breathing may all be valuable to the strand invasion process. The results of this study will provide a new approach for the targeting of double-stranded DNA, one that can be used for both purine-pyrimidine and pyrimidine-purine base pairs equally. It will generalize the process of sequence recognition to include essentially any DNA sequence.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM053201-08
Application #
6636147
Study Section
Bio-Organic and Natural Products Chemistry Study Section (BNP)
Program Officer
Schwab, John M
Project Start
1995-07-01
Project End
2006-06-30
Budget Start
2003-07-01
Budget End
2006-06-30
Support Year
8
Fiscal Year
2003
Total Cost
$211,550
Indirect Cost
Name
Boston College
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
045896339
City
Chestnut Hill
State
MA
Country
United States
Zip Code
02467
Stewart, Kristen M; McLaughlin, Larry W (2004) Four-arm oligonucleotide Ni(II)-cyclam-centered complexes as precursors for the generation of supramolecular periodic assemblies. J Am Chem Soc 126:2050-7
Chen, Dongli; Meena, Meena; Sharma, Sunil K et al. (2004) Formation and stability of a Janus-Wedge type of DNA triplex. J Am Chem Soc 126:70-1
Sharma, Sunil K; McLaughlin, Larry W (2004) Triplex mediated delivery of a platinum complex to a specific DNA target site. J Inorg Biochem 98:1570-7
Sharma, Sunil K; McLaughlin, Larry W (2002) Cross-linking of a DNA conjugate tethering a cis-bifunctional platinated complex to a target DNA duplex. J Am Chem Soc 124:9658-9
Gianolio, D A; Segismundo, J M; McLaughlin, L W (2000) Tethered naphthalene diimide-based intercalators for DNA triplex stabilization. Nucleic Acids Res 28:2128-34
Chen, D L; McLaughlin, L W (2000) Use of pK(a) differences to enhance the formation of base triplets involving C-G and G-C base pairs. J Org Chem 65:7468-74
Gianolio, D A; McLaughlin, L W (1999) Synthesis and triplex forming properties of pyrimidine derivative containing extended functionality. Nucleosides Nucleotides 18:1751-69
Wiederholt, K; McLaughlin, L W (1999) A 2,2""-bipyridine ligand for incorporation into oligodeoxynucleotides: synthesis, stability and fluorescence properties of ruthenium-DNA complexes. Nucleic Acids Res 27:2487-93
St Clair, A; Xiang, G; McLaughlin, L W (1998) Synthesis and triplex forming properties of an acyclic N7-glycosylated guanine nucleoside. Nucleosides Nucleotides 17:925-37
Xiang, G; Bogacki, R; McLaughlin, L W (1996) Use of a pyrimidine nucleoside that functions as a bidentate hydrogen bond donor for the recognition of isolated or contiguous G-C base pairs by oligonucleotide-directed triplex formation. Nucleic Acids Res 24:1963-70