Synthesis and nucleic acid binding properties of novel peptide nucleic acids carrying beta amino acid spacer
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Title Synthesis and nucleic acid binding properties of novel peptide nucleic acids carrying beta amino acid spacer
Creator Chaturong Suparpprom
Contributor Tirayut Vilaivan
Publisher Chulalongkorn University
Publication Year 2549
Keyword Nucleic acids -- Synthesis, Nucleic acids -- Properties, กรดนิวคลีอิก -- การสังเคราะห์, กรดนิวคลีอิก -- คุณสมบัติ, ปริญญาดุษฎีบัณฑิต
Abstract A synthetic method for novel Peptide Nucleic Acid (PNA) carrying Beta-amino acid spacers has been developed. The PNA monomers in this research were pyrrolidine derivatives modified with 4 natural nucleobases at C-4 position. The thymine monomers were synthesized in all possible stereoisomers including "cis-D", "trans-D", "cis-L" and "trans-L". The adenine, cytosine and guanine monomers were synthesized only in "cis-D" configuration. These PNA monomers were coupled with Beta-amino acid spacers in an alternate fashion by Fmoc solid phase peptide synthesis. The spacers included in this studies were classified into three categories: acyclic (amino-oxy acetic acid, N-amino N-methylglycine), cyclic with one stereogenic center (D-aminopyrrolidine carboxylic acid or D-APC, L-aminopyrrolidine carboxylic acid or (L-APC), cyclic with two stereogenic centers [(1S,2S), (1R,2R), (1S,2R) and (1R,2S)-2-aminocylopentane carboxylic acids (ACPC)]. The solid-phase synthesis proceeded efficiently with more than 90% average efficiency for each individual coupling step. PNA sequences in 5-10 base lengths were successfully synthesized and were characterized by MALDI-TOF MS. Binding properties of these PNA with DNA were studied by UV-titration, T[subscript m], gel electrophoresis, circular dichroism and fluorescence experiments. These revealed that the cis-D pyrrolidine PNA containing the D-aminopyrrolidine carboxylic acid (D-APC) or (1S,2S)-2-aminocyclopentane carboxylic acid [(1S,2S)-ACPC] spacers can form stable 1:1 hybrids with DNA. The PNA-DNA interactions followed the Watson-Crick base-pairing rules (A.T, C.G). The cis-D/D-APC PNA also exhibited a strong preference for binding to DNA in antiparallel fashion.
URL Website cuir.car.chula.ac.th
Chulalongkorn University

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