PATENTSCOPE sera indisponible quelques heures pour des raisons de maintenance le mardi 19.11.2019 à 16:00 CET
Recherche dans les collections de brevets nationales et internationales
Certains contenus de cette application ne sont pas disponibles pour le moment.
Si cette situation persiste, veuillez nous contacter àObservations et contact
1. (WO2005067437) METHODES ET COMPOSITIONS PERMETTANT D'UTILISER IN VITRO ET IN VIVO DES EPINGLES A CHEVEUX ET DES STRUCTURES TRIPLEX A BRINS PARALLELES EN TANT QUE LIGANDS D'ACIDES NUCLEIQUES
Note: Texte fondé sur des processus automatiques de reconnaissance optique de caractères. Seule la version PDF a une valeur juridique

CLAIMS

We claim:

1. A nucleic acid ligand comprising a parallel-stranded hairpin.

2. The nucleic acid ligand of claim 1, wherein said parallel-stranded hairpin

comprises a polypurine part and a polypyrimidine connected at their 5' ends by a linker.

3. The nucleic acid ligand of claim 1, wherein said parallel-stranded hairpins

comprise a polypurine part and a polypyrimidine connected at their 3' ends by a linker.

4. The nucleic acid ligand of claim 1, wherein said parallel-stranded hairpins

comprise at least one modified aminopurine.

5. The nucleic acid ligand of claim 1, wherein said parallel-stranded hairpins

comprise at least one 8-aminopurine.

6. The nucleic acid ligand of claim 5, wherein said 8-aminopurine is selected from the group consisting of 8-aminoadenine, 8-aminoguanine, and 8- aminohypoxanthine.

7. The nucleic acid ligand of claim 1, wherein said nucleic acid ligand is an

oligonucleotide triplex.

8. The nucleic acid ligand of claim 7, wherein said oligonucleotide triplex

comprises at least one 8-aminopurine.

9. The nucleic acid ligand of claim 1, further comprising a polypeptide.

10. The nucleic acid ligand of claim 9, wherein said polypeptide is a binder

polypeptide.

11. The nucleic acid ligand of claim 9, wherein said polypeptide is a label polypeptide.

12. A method for preparing a parallel oligonucleotide duplex, comprising:

(a) providing a branching phosphoramidite with a first track and a second track; (b) protecting each of said first track and said second track with a protecting group, wherein the protecting group of the first track is different from the protecting group of the second track;

(c) removing the protecting group of the first track and bonding a purine to said first track;

(d) replacing a protecting group on the first track;

(e) removing the protecting group of the second track and bonding a pyrimidine to said second track, wherein said pyrimidine is complementary to the purine of step (c);

(f) replacing a protecting group on the second track; and

(g) repeating steps (c) through (e) to form a parallel oligonucleotide duplex.

13. The method of claim 12, further comprising the step of performing a mix and split procedure before step (g).

14. The method of claim 12, wherein said protecting groups are selected from the group consisting of an acid labile protecting group, a base labile protecting group, a fluoride labile protecting group, a hydrazine labile protecting group, and a photolabile protecting group.

15. The method of claim 14, wherein said acid labile protecting group is selected from the group consisting of dimethoxytrityl and monomethoxytril.

16. The method of claim 14, wherein said base labile protecting group is fluorenylmethoxycarbonyl .

17. The method of claim 14, wherein said fluoride labile protecting group is tert- butyldimethylsilyl.

18. The method of claim 14, wherein said hydrazine labile protecting group is levulenyl.

19. The method of claim 14, wherein said photolabile protecting group is

c-Nitrobenzyl.

20. The method of claim 14, wherein said parallel oligonucleotide duplex

comprises at least member of the group consisting of 8-aminoguanine, 8- aminoadenine, 8-aminohypoxanthine and 5-methylcytosine.

21. A method for binding a target molecule comprising:

(a) providing a target molecule;

(b) providing a nucleic acid ligand comprising a parallel-stranded hairpin, wherein said parallel-stranded hairpin has a secondary or tertiary structure that allows binding with said target molecule;

(c) combining said target molecule and said nucleic acid ligand; and

(d) binding said target molecule to said nucleic acid ligand.

22. The method of claim 21, including wherein said parallel-stranded hairpin includes at least one 8-aminopurine.

23. The method of claim 22, including wherein said at least one 8-aminopurine is selected from the group consisting of 8-aminoadenine, 8-aminoguanine, and 8- aminohypoxanthine.

24. The method of claim 21, including wherein said nucleic acid ligand is an oligonucleotide triplex

25. The method of claim 21, including wherein said target molecule is selected from the group consisting of human proteins, animal proteins, viral proteins, bacterial proteins, peptides, proteins with enzymatic activity, lipases, kinases, esterases, phosphatases, proteases, toxins, prions, hormones, antigen, antibodies, cell receptors, cell surface antigens, adaptor binding proteins, adhesion molecules, apohpoproteins, apoptosis-related proteins, cancer-related proteins, cell cycle proteins, growth factors, Prekallikrein (Fletcher Factor), Kallikrein, Kininogen, Factor I (Fibrinogen), Factor II (Prothrombin), Factor III (Tissue

Factor), Factor V, Factor VI (Accelerin), Factor VII, Factor VIII, Factor IX, Factor X, Factor XI (Plasma thromboplastin), Factor XII, Factor XIII, and plasminogen, Plasminogen Activator inhibitor-1 (PAH), Plasminogen Activator inhibitor-2 (PAI2), disease related proteins, cell matrix proteins, cytoskelaton proteins, phosphoproteins, signal transduction related proteins, transcriptional factors, protein translation protein factors, transporters, tissue-specific proteins, complement proteins, carbohydrates, polysaccharides, lipids, Elastase, von Willebrand Factor, Protein C, Protein S, Thrombomodulin, Antithrombin III, Eph-receptor and ephrin-ligand, PTEN, Protein tyrosine phosphatases SHP-1, PRL-3, p53, CDKN2A, MMAC1/PTEN/TEP1 protein, Pim-2, HIV Protease,

NS3 protease of hepatitis C vims, Ricin Toxin, 5-alpha reductase, HIV-1 reverse transcriptase, cyclooxygenase, S-adenosylhomocysteine, caffeine, cocaine, and neurotransmitters.

26. The method of claim 21, including wherein said nucleic acid ligand is stable in a human patient.

27. The method of claim 21, including wherein said nucleic acid ligand is bound to a solid support.

28. The method of claim 21, including wherein said nucleic acid ligand is

administered to a human patient in need of treatment.

29. The method of claim 28, including wherein said nucleic acid ligand is

administered while bound to a carrier.

30. The method of claim 29, including wherein said carrier is selected from the group consisting of an erythrocyte and an erythrocyte ghost.

31. The method of claim 30, including the further step of eliminating said nucleic acid ligand, target, and carrier from the body of a patient through the apoptotic cell pathway.

32. The method of claim 30, including the further step of eliminating said nucleic acid ligand, target, and carrier from the body of a patient through complement activity.

33. A nucleic acid ligand comprising a parallel-stranded hairpin, wherein said parallel-stranded hairpin is selected from the group consisting of PSH01, PSH02, PSH03, PSH04, PSH05, PSH06, PSH07, PSH08, PSH09, PSH10, PSH11, PSH12, PSH13, PSH14, PSH15, PSH16, PSH17, PSH18, PSH19,

PSH20,PSH21, PSH22, PSH23, PSH24, PSH25, PSH26, PSH27, PSH28, PSH29, PSH30, PSH31, PSH32, PSH33, PSH34, PSH35, PSH36, PSH37,

PSH38, PSH39, PSH40, PSH41, PSH42, PSH43, PSH44, PSH45, PSH46,

PSH47.

34. A nucleic acid ligand including an oligonucleotide triplex, said oligonucleotide triplex selected from the group consisting of TS01, TS02, and TS03.

35. Parallel-stranded hairpin sequences as aptamers.

36. Oligonucleotide triplexes as aptamers.