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Volumn 59, Issue 27, 2003, Pages 5123-5128

Selective recognition of CG interruption by 2′,4′-BNA having 1-isoquinolone as a nucleobase in a pyrimidine motif triplex formation

Author keywords

Antigene; Molecular recognition; Nucleic acid analogues; Triplex

Indexed keywords

BRIDGED COMPOUND; DOUBLE STRANDED DNA; NUCLEIC ACID; NUCLEIC ACID BASE; OLIGONUCLEOTIDE; QUINOLONE DERIVATIVE;

EID: 0038380198     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(03)00728-2     Document Type: Article
Times cited : (19)

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    • Recently, 1-isoquinolone and its derivatives with a 2-deoxyribose moiety have been noted as a universal base, capable of isoenergetic hybridization with any natural nucleobase, and as a hydrophobic base to form an enzymatically replicable unnatural base pair for expansion of the genetic alphabet. McMinn D.L., Ogawa A.K., Wu Y., Liu J., Schultz P.G., Romesberg F.E. J. Am. Chem. Soc. 121:1999;11585-11586 Berger M., Wu Y., Ogawa A.K., McMinn D.L., Schultz P.G., Romesberg F.E. Nucleic Acids Res. 28:2000;2911-2914 Ogawa A.K., Wu Y., McMinn D.L., Liu J., Schultz P.G., Romesberg F.E. J. Am. Chem. Soc. 122:2000;3274-3287.
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    • Recently, 1-isoquinolone and its derivatives with a 2-deoxyribose moiety have been noted as a universal base, capable of isoenergetic hybridization with any natural nucleobase, and as a hydrophobic base to form an enzymatically replicable unnatural base pair for expansion of the genetic alphabet. McMinn D.L., Ogawa A.K., Wu Y., Liu J., Schultz P.G., Romesberg F.E. J. Am. Chem. Soc. 121:1999;11585-11586 Berger M., Wu Y., Ogawa A.K., McMinn D.L., Schultz P.G., Romesberg F.E. Nucleic Acids Res. 28:2000;2911-2914 Ogawa A.K., Wu Y., McMinn D.L., Liu J., Schultz P.G., Romesberg F.E. J. Am. Chem. Soc. 122:2000;3274-3287.
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