Sequence-specific cleavage of yeast tRNA(Phe) with oligonucleotides conjugated to a diimidazole construct

Antisense and Nucleic Acid Drug Development

Volumn 7, Issue 1, 1997, Pages 39-42

  Vlassov, Valentin ^a   Abramova, Tatyana ^a   Godovikova, Tatyana ^a   Giege, Richard ^b   Silnikov, Vladimir ^a  

^a INSTITUTE OF CHEMICAL BIOLOGY AND FUNDAMENTAL MEDICINE   (Russian Federation)

^b CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

HISTAMINE; IMIDAZOLE DERIVATIVE; OLIGONUCLEOTIDE; PHENYLALANINE TRANSFER RNA; RIBONUCLEASE A;

ARTICLE; CHEMICAL STRUCTURE; DRUG CONJUGATION; ENZYME ACTIVE SITE; NONHUMAN; PHYSIOLOGY; PRIORITY JOURNAL; RNA DEGRADATION; RNA STRUCTURE; YEAST;

EID: 0030981918     PISSN: 10872906     EISSN: None     Source Type: Journal    
DOI: 10.1089/oli.1.1997.7.39     Document Type: Article

References (7)

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2. BRESLOW, R. (1991). How do imidazole groups catalyze the cleavage of RNA in enzyme models and in enzymes? Evidence from "negative catalysis" Acc. Chem. Res. 24, 317-324.
3. CROOKE, S.T., and LEBLEU, B., eds. (1993). Antisense Research and Applications. (CRC Press, Boca Raton, FL).
4. GODOVIKOVA, T.S., ZARYTOVA, V.F., MALTSEVA, T.V., and KHALIMSKAYA, L.M. (1989). Reactive derivatives of oligonucleotides with a zwitterionic terminal phosphate group for affinity reagents and probe construction. Bioorgan Khim. 15, 1246-1252.
5. HALL, J., HUSKEN, D., PIELES, U., MOSER, H.E., and HANER, R. (1994). Efficient sequence-specific cleavage of RNA using novel europium complexes conjugated to oligonucleotides. Chem. Biol. 1, 185-190.
6. KISFALUDY, L., LÖW., M., and NYEKI, O. (1973). Die Vervendung von Pentafluorphenylestern bei Peptidsynthesen. Liebigs Ann. Chem. 1421-1429.
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