IP Library Granted Patent US 8,334,373
Granted Patent B2
US 8,334,373 · App. 13/038,672 · Granted Dec 18, 2012

Nuclease resistant double-stranded ribonucleic acid

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Quick Facts
Patent No.
US 8,334,373
App. No.
13/038,672
Granted
Dec 18, 2012
Kind
B2
Abstract

This invention relates to modified double-stranded oligoribonucleic acid (dsRNA) having improved stability in cells and biological fluids, and methods of making and identifying dsRNA having improved stability, and of using the dsRNA to inhibit the expression or function of a target gene.

Claims (40)

1. A double-stranded ribonucleic acid (dsRNA) having a sense strand and an antisense strand and having increased stability in a biological sample, wherein the sense strand and the antisense strand are both modified, said antisense-strand modifications consisting of:

(a) 2′-modified uridines in all occurrences of the sequence motif 5′-uridine-adenine-3′ (5′-ua-3′), and

(b) 2′-modified cytidines in all occurrences of the sequence motif 5′-cytidine-adenine-3′ (5′-ca-3′).

2. The dsRNA of claim 1 , wherein the sense-strand modifications comprise at least one of the features (a) and (b).

3. The dsRNA of claim 1 , wherein the dsRNA comprises at least two occurrences of at least one of the sequence motifs.

4. The dsRNA of claim 1 , wherein the dsRNA comprises at least three occurrences of at least one of the sequence motifs.

5. The dsRNA of claim 1 , wherein the sense strand further comprises at least one dinucleotide selected from the group consisting of 5′-uu-3′, 5′-ug-3′, 5′-uc-3′, 5′-cu-3′, 5′-cg-3′, and 5′-cc-3′, wherein no nucleotide of the at least one dinucletide is a 2′-O-modified nucleotide.

6. The dsRNA of claim 1 , wherein the 2′-modified nucleotide is a 2′-deoxy nucleotide, a 2′-O-methyl nucleotide, a 2′-deoxyfluoro nucleotide, a 2′-O-methoxyethyl (2′-O-MOE) nucleotide, a 2′-O—N-methylacetamido (2′-O-NMA) nucleotide, a 2′-O-dimethylaminoethoxyethyl (2′-O-DMAEOE) nucleotide, a 2′-O-aminopropyl (2′-O-AP) nucleotide, a 2′-ara-F nucleotide, or a locked nucleic acid nucleotide.

7. The dsRNA of claim 2 , wherein the sense strand mocifications further comprising at least one of

(c) 2′-modified uridines in all occurrences of the sequence motif 5′-uridine-guanine-3′ (5′-ug-3′), or

(d) 2′-modified 5′-most uridines in all occurrences of the sequence motif 5′-uridine-uridine-3′ (5′-uu-3′), or

(e) 2′-modified 5′-most cytidines in all occurrences of the sequence motif 5′-cytidine-cytidine-3′ (5′-cc-3′), or

(f) 2′-modified cytidines in all occurrences of the sequence motif 5′-cytidine-uridine-3′ (5′-cu-3′), or

(g) 2′-modified uridines in all occurrences of the sequence motif 5′-uridine-cytidine-3′ (5′-uc-3′).

8. The dsRNA of claim 7 , wherein the sense strand comprises at least one of features (c) and (d).

9. The dsRNA of claim 7 , wherein the sense strand comprises features (c) and (d).

10. A method of preparing a pharmaceutical composition, comprising formulating the dsRNA of claim 1 in a pharmaceutically acceptable carrier.

11. A pharmaceutical composition for inhibiting the expression of a target gene in a mammal, comprising:

(a) at least one dsRNA of claim 1 ; and

(b) a pharmaceutically acceptable carrier.

12. A double-stranded ribonucleic acid (dsRNA) having a sense strand and an antisense strand and having increased stability in a biological sample, wherein the sense strand and the antisense strand are both 2′-modified, said antisense-strand 2′-modifications consisting of:

(a) 2′-modified uridines in all occurrences of the sequence motif 5′-uridine-adenine-3′ (5′-ua-3′), and

(b) 2′-modified cytidines in all occurrences of the sequence motif 5′-cytidine-adenine-3′ (5′-ca-3′).

13. The dsRNA of claim 12 , wherein the sense-strand modifications comprise at least one of the features (a) and (b).

14. The dsRNA of claim 12 , wherein the dsRNA comprises at least two occurrences of at least one of the sequence motifs.

15. The dsRNA of claim 12 , wherein the dsRNA comprises at least three occurrences of at least one of the sequence motifs.

16. The dsRNA of claim 12 , wherein the sense strand further comprises at least one dinucleotide selected from the group consisting of 5′-uu-3′, 5′-ug-3′, 5′-uc-3′, 5′-cu-3′, 5′-cg-3′, and 5′-cc-3′, wherein no nucleotide of the at least one dinucleotide is a 2′-O-modified nucleotide.

17. The dsRNA of claim 12 , wherein the 2′-modified nucleotide is a 2′-deoxy nucleotide, a 2′-O-methyl nucleotide, a 2′-deoxyfluoro nucleotide, a 2′-O-methoxyethyl (2′-O-MOE) nucleotide, a 2′-O-N-methylacetamido (2′-O-NMA) nucleotide, a 2′-O-dimethylaminoethoxyethyl (2′-O-DMAEOE) nucleotide, a 2′-O-aminopropyl (2′-O-AP) nucleotide, a 2′-ara-F nucleotide, or a locked nucleic acid nucleotide.

18. The dsRNA of claim 13 , wherein the sense strand 2′-modifications further comprise at least one of

(c) 2′-modified uridines in all occurrences of the sequence motif 5′-uridine-guanine-3′ (5′-ug-3′), or

(d) 2′-modified 5′-most uridines in all occurrences of the sequence motif 5′-uridine-uridine-3′ (5′-uu-3′), or

(e) 2′-modified 5′-most cytidines in all occurrences of the sequence motif 5′-cytidine-cytidine-3′ (5′-cc-3′), or

(f) 2′-modified cytidines in all occurrences of the sequence motif 5′-cytidine-uridine-3′ (5′-cu-3′), or

(g) 2′-modified uridines in all occurrences of the sequence motif 5′-uridine-cytidine-3′ (5′-uc-3′).

19. The dsRNA of claim 7 , wherein the sense strand comprises at least one of features (c) and (d).

20. The dsRNA of claim 7 , wherein the sense strand comprises features (c) and (d).

21. A method of preparing a pharmaceutical composition, comprising formulating the dsRNA of claim 12 in a pharmaceutically acceptable carrier.

22. A pharmaceutical composition for inhibiting the expression of a target gene in a mammal, comprising:

(a) at least one dsRNA of claim 12 ; and

(b) a pharmaceutically acceptable carrier.

Assignments (2)
SECURITY INTEREST Recorded Oct 1, 2025
From: ALNYLAM PHARMACEUTICALS, INC.; SIRNA THERAPEUTICS, INC.
To: BANK OF AMERICA, N.A.
Reel/Frame 072996/0337 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 14, 2011
From: VORNLOCHER, HANS-PETER; ROEHL, INGO; HADWIGER, PHILIPP; ZIMMERMANN, TRACY STAGE; MANOHARAN, MUTHIAH; RAJEEV, KALLANTHOTTATHIL G.; AKINC, AKIN
To: ALNYLAM PHARMACEUTICALS, INC.
Reel/Frame 027382/0330 →