IP Library Granted Patent US 8,501,706
Granted Patent B2
US 8,501,706 · App. 13/552,709 · Granted Aug 6, 2013

Duplex oligonucleotide complexes and methods for gene silencing by RNA interference

Inventors: Christina Yamada (Boulder, CO); Anastasia Khvorova (Northborough, MA); Rob Kaiser (Broomfield, CO); Emily Anderson (Lafayette, CO); Devin Leake (Denver, CO)
Assignee: Dharmacon, Inc.
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Quick Facts
Patent No.
US 8,501,706
App. No.
13/552,709
Granted
Aug 6, 2013
Kind
B2
Abstract

Provided herein are duplex oligonucleotide complexes which can be administered to a cell, tissue or organism to silence a target gene without the aid of a transfection reagent(s). The duplex oligonucleotide complexes of the disclosure include a conjugate moiety that facilitates delivery to a cell, tissue or organism.

Claims (34)

1. A method for inhibiting expression of a target gene in a cell, the method comprising delivering to said cell a duplex oligonucleotide complex comprising:

a. a sense strand that is nineteen nucleotides in length, wherein nucleotides 1 and 2 and all C and all U nucleotides on said sense strand are 2′O-methyl modified and the sense strand has a 3′ end;

b. an antisense strand that is twenty-one nucleotides in length, wherein

i. all C nucleotides and all U nucleotides on said antisense strand are 2′F modified;

ii. the antisense strand has a 5′ end and a 3′ end and one mismatched nucleotide with the sense strand at position 14 within the antisense strand and the opposite nucleotide 6 on the sense strand, wherein all other nucleotides within the sense strand are complementary to nucleotides on the antisense strand; and

iii. the sense strand and the antisense strand form a duplex having a two nucleotide overhang at the 3′end of the antisense strand;

c. a cholesterol molecule attached to the 3′ end of the sense strand via a C5 linker molecule, wherein the cholesterol-linker-sense strand has the structure:

and

d. a phosphate group at the 5′ end of the antisense strand, wherein following said delivering the expression of a target protein is decreased.

2. The method of claim 1 , wherein the delivering is passive.

3. The method of claim 1 , wherein the two nucleotide overhang comprises a phosphorothioate linkage.

4. The method of claim 1 , wherein the two nucleotide overhang comprises a UU sequence.

5. A method for inhibiting expression of a target gene in a cell, the method comprising delivering to said cell a duplex oligonucleotide complex comprising:

a. a sense strand that is nineteen nucleotides in length, wherein nucleotides 1 and 2 and all C and all U nucleotides on said sense strand are 2′O-methyl modified and the sense strand has a 3′ end;

b. an antisense strand that is twenty-one nucleotides in length, wherein

i. all C nucleotides and all U nucleotides on said antisense strand are 2′F modified;

ii. the antisense strand has a 5′ end and a 3′ end and one mismatched nucleotide with the sense strand at position 13 within the antisense strand and the opposite nucleotide 7 on the sense strand, wherein all other nucleotides within the sense strand are complementary to nucleotides on the antisense strand; and

iii. the sense strand and the antisense strand form a duplex having a two nucleotide overhang at the 3′ end of the antisense strand;

c. a cholesterol molecule attached to the 3′ end of the sense strand via a C5 linker molecule, wherein the cholesterol-linker-sense strand has the structure:

and

d. a phosphate group at the 5′ end of the antisense strand, wherein following said delivering the expression of a target protein is decreased.

6. The method of claim 5 , wherein the delivering is passive.

7. The method of claim 5 , wherein the two nucleotide overhang comprises a phosphorothioate linkage.

8. The method of claim 5 , wherein the two nucleotide overhang comprises a UU sequence.

9. The method according to claim 1 , wherein the opposite nucleotide 6 on the sense strand is the same nucleotide that occurs at position 14 of the antisense strand.

10. The method according to claim 5 , wherein the opposite nucleotide 7 on the sense strand is the same nucleotide that occurs at position 13 of the antisense strand.

11. The method according to claim 1 , wherein all nucleotides in the sense strand and in the antisense strand other than nucleotides 1 and 2 of the sense strand and all C nucleotides and all U nucleotides of the sense and antisense strands comprise a 2′-OH.

12. The method according to claim 5 , wherein all nucleotides in the sense strand and in the antisense strand other than nucleotides 1 and 2 of the sense strand and all C nucleotides and all U nucleotides of the sense and antisense strands comprise a 2′-OH.

13. The method according to claim 1 , wherein between about 40% and about 90% of the nucleotides of the sense strand and between about 40% and about 90% of the nucleotides of the antisense strand are chemically modified.

14. The method according to claim 5 , wherein between about 40% and about 90% of the nucleotides of the sense strand and between about 40% and about 90% of the nucleotides of the antisense strand are chemically modified.

15. The method of claim 1 , wherein said delivering to said cell is by reverse transfection.

16. The method of claim 5 , wherein said delivering to said cell is by reverse transfection.

17. The method of claim 1 , wherein said delivering to said cell is in vivo.

18. The method of claim 5 , wherein said delivering to said cell is in vivo.

Assignments (4)
CHANGE OF NAME Recorded Oct 2, 2017
From: GE HEALTHCARE DHARMACON, INC.
To: DHARMACON, INC.
Reel/Frame 044105/0171 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 9, 2014
From: THERMO FISHER SCIENTIFIC BIOSCIENCES INC.
To: GE HEALTHCARE DHARMACON, INC.
Reel/Frame 032863/0603 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 15, 2014
From: YAMADA, CHRISTINA; KHVOROVA, ANASTASIA; KAISER, ROB; ANDERSON, EMILY; LEAKE, DEVIN
To: DHARMACON, INC.
Reel/Frame 032671/0904 →
CHANGE OF NAME Recorded Aug 9, 2013
From: DHARMACON, INC.
To: THERMO FISHER SCIENTIFIC BIOSCIENCES INC.
Reel/Frame 030994/0823 →
Continuity (4)
Division 11858829 · Sep 20, 2007
Provisional Application 60826702 · Sep 22, 2006
Provisional Application 60867706 · Nov 29, 2006
Related Publication 20120322855A1 · Dec 20, 2012