2005 Fiscal Year Final Research Report Summary
Synthesis and properties of artificial nucleic acids utilizing pentaerythritol.
Project/Area Number |
16590082
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Drug development chemistry
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Research Institution | Gifu University |
Principal Investigator |
UENO Yoshihito Gifu University, Department of Biomolecular Science, Faculty of Engineering, Associate Professor, 工学部, 助教授 (20250467)
|
Project Period (FY) |
2004 – 2005
|
Keywords | nucleoside / nucleotide / DNA / triplex / protein / linker / antigene method |
Research Abstract |
First, the synthesis and thermal stabilities of the triplexes containing either 2'-deoxyinosine (1) or 2'-deoxyxanthosine (3) in their second strands were examined. It was found that the triplexes with the 2'-deoxy-5-methylcytidine(dM)・1:dC and dM・1:dA base triplets are thermally stable, but those containing the dM・1:T and dM・1:dG base triplets are unstable under both neutral and slightly acidic conditions. On the other hand, it was found that the oligonucleotide containing 3 could form thermally stable triplexes with the oligonucleotides that involve four natural bases opposite the sites of 3. The rank of the thermal stabilities of the triplexes was as follows : the triplex containing the dM・3:dC base triplet > that containing the dM・3:dA base triplet > that containing the dM・3:T base triplet > that containing the dM・3:dG base triplet. Furthermore, the synthesis of triplexes possessing an anthraquinonyl group and composed of branched oligonucleotides (ONs) was examined. Binding ability of a triplex-binding protein (MBP-LOR3^<ARF>) to the triplexes was evaluated by an electrophoretic mobility shift assay (EMSA). It was found that the triplex, which has an antraquinonecarbonyl group at the 5'-end of the third strand and is connected with the pentaerythritol linker, has greater affinity to the protein than an unmodified triplex.
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Research Products
(8 results)