Organic compounds -- part of the class 532-570 series – Organic compounds – Carbohydrates or derivatives
Reexamination Certificate
2005-03-15
2005-03-15
Horlick, Kenneth R. (Department: 1637)
Organic compounds -- part of the class 532-570 series
Organic compounds
Carbohydrates or derivatives
C435S006120, C435S091100, C536S024300
Reexamination Certificate
active
06867290
ABSTRACT:
Provided is a polynucleotide comprising mRNA, rRNA or viral RNA, comprising ribose rings that are covalently modified at the 2′-OH position. Further provided are methods for producing a double-stranded oligo- or polynucleotide from a template comprising an oligo- or polyribonucleotide, a proportion of the ribose rings of which are covalently modified at the 2′-OH position to bear a substituent which enables replication of the template by the nucleic acid polymerase. Also provided is use of a poly-nucleotide comprising mRNA, rRNA or viral RNA, a proportion of the ribose rings of which are covalently modified at the 2′-OH position, in a hybridisation reaction.
REFERENCES:
patent: 5426180 (1995-06-01), Kool
patent: 5660985 (1997-08-01), Pieken et al.
patent: 5681726 (1997-10-01), Huse et al.
patent: 5700642 (1997-12-01), Monforte et al.
patent: 5707796 (1998-01-01), Gold et al.
patent: 5783425 (1998-07-01), Dudycz et al.
patent: 5859221 (1999-01-01), Cook et al.
patent: 5872232 (1999-02-01), Cook et al.
patent: 6008334 (1999-12-01), Hanna
patent: 9203568 (1992-03-01), None
patent: WO 9419012 (1994-01-01), None
patent: 9813526 (1998-04-01), None
patent: 9914346 (1999-03-01), None
patent: 9936517 (1999-07-01), None
patent: 9955857 (1999-11-01), None
patent: WO 0075302 (2000-12-01), None
Yu et al., “mRNA acetylated at 2′-OH group of ribose residues is functionally active in the cell-free translation system from whe embryos,” FEBS, Sep. 1990, vol. 270, p. 111-114.*
Lewis, R. “Kits take the trickiness out of RNA isolation, purification”, The Scientist 11(7):16-20 (1997).
Pagratis, N.C. et al. “Potent 2′-amino-, and 2′-flouro-2′-deoxyribonucleotide RNA inhibitors of keratinocyte growth factor”, Nature Biotechnology 15(1): 68-73 (1997).
Sproat, B.S., “Chemistry and applications of oligonucleotide analogues”, Journal of Biotechnology 41:221-238 (1995).
Ovodov, S.Y., “mRNA acetylated at 2′-OH-groups of ribose residues is functionally active in the cell-free translation system from wheat embryos”, FEBS 270(1,2):111-114 (1990).
Ru, K. et al. “Specific inhibition of breast cancer cells by antisense poly-DNP-oligoribonucleotides and targeted apoptosis”, Oncology Res. 10:389-397 (1998).
Roche Applied Science Advertisement: Protector RNase Inhibitor: Enhance the protection of RNA against Degradation.
Knorre, D.G., et al. “Production of transfer RNA acetylated at its 2′-hydroxy groups” Biochemistry USSR 1045-1050 (1965): translated from Biokhimiya 30:6 (1965).
Knorre, D.G., et al., “Investigation of the role of 2′-OH groups in the formation of secondary structure in polyribonucleotides” Biochim. Biophys. Acta 142:555 (1987).
Roland, A., et al., “Measurement of Copper-Binding Sites on Low Density Lipoprotein”, Arterioscler Thromb Vasc Biol, pp. 594-602 (2001).
Knorre, D.G., et al. “Effect of Acetylation of the Ribose 2′-Hydroxyl Groups of Polyribonucleotides on Their Template Activity”, Molekul.Biol 1: 837 (1967).
Heidenrich, Olaf et al., “Chemically Modified RNA: Approaches and Applications”, The FASEB Journal, Jan. 1993, vol. 7.
Heidenrich, Olaf et al., “High Activity and Stability of Hammerhead Ribozymes Containing 2′-Modified Pyrimidine Nucleosides and Phosphorothioates”, The Journal of Biological Chemistry, vol. 269, No. 3, Jan. 21, pp.2131-2138, 1994.
Aurup, Helle et al., “Translation of 2′-Modified mRNA in vitro and in vivo”, Nucleic Acids Research, 1994, vol. 22, No. 23. pp. 4963-4968.
Xin, Wei et al., “Treatment of Duck Hepatitis B Virus by Antisense Poly-2′-O-(2,4-Dinitrophenyl)-Oligoribonucleotides”, Bioenergetics Laboratory, Natural Sciences Center, State University of NY, Buffalo, Jul. 1998.
Iribarren, Adolfo M. et al., “2′-0-Alkyl Oligoribonucleotides as Antisense Probes”, Proc. Natl. Acad. Sci.., vol. 87, pp 7747-7751, Oct. 1990.
Inoue, Hideo et al, “Synthesis and Hybridization Studies on Two Complementary Nona(2′-0-methyl) Ribonucleotides”, Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060, Japan, Jun. 1987.
Cyclops Genome Sciences, Ltd.
Horlick Kenneth R.
Kim Young J.
Saliwanchik Lloyd & Saliwanchik
LandOfFree
Modified polynucleotides and uses thereof does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Modified polynucleotides and uses thereof, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Modified polynucleotides and uses thereof will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-3438984