IP Library Granted Patent US 9,382,537
Granted Patent B2
US 9,382,537 · App. 14/459,182 · Granted Jul 5, 2016

Methods and compositions involving miRNA and miRNA inhibitor molecules

Inventors: David Brown (Austin, TX); Lance Ford (Austin, TX); Angie Cheng (Austin, TX); Rich Jarvis (Austin, TX); Mike Byrom (Austin, TX); Dmitriy Ovcharenko (Austin, TX); Eric Devroe (Pflugerville, TX); Kevin Kelnar (Kyle, TX)
Assignee: ASURAGEN, INC.
C12N15/113A61K9/127A61K31/7088A61K31/713A61K31/7105A61K45/06A61N5/10C12N15/111C12N15/1136C12Q1/68C12N2310/14C12N2310/141C12N2310/321C12N2310/322C12N2310/33C12N2310/344C12N2310/35C12N2310/351C12N2310/3527C12N2310/3535C12N2310/533C12N2320/12C12N2320/30C12N2320/50C12N2330/10
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Quick Facts
Patent No.
US 9,382,537
App. No.
14/459,182
Granted
Jul 5, 2016
Kind
B2
Abstract

The present invention concerns methods and compositions for introducing miRNA activity or function into cells using synthetic nucleic acid molecules. Moreover, the present invention concerns methods and compositions for identifying miRNAs with specific cellular functions that are relevant to therapeutic, diagnostic, and prognostic applications wherein synthetic miRNAs and/or miRNA inhibitors are used in library screening assays.

Claims (16)

1. A synthetic miR-101 molecule comprising:

(a) an active strand comprising a sequence identical to human miR-101; and

(b) a separate complementary strand that is at least 60% complementary to the active strand and has a 5′-terminal nucleotide that is chemically modified to comprise a lower alkylamine group.

2. The synthetic miR-101 molecular of claim 1 , wherein the lower alkylamine group is attached to a 5′ phosphate of the 5′-terminal nucleotide of the complementary strand.

3. The synthetic miR-101 molecule of claim 1 , wherein the active strand is 22-30 nucleotides in length.

4. The synthetic miR-101 molecule of claim 1 , wherein the active strand is 23 nucleotides in length.

5. A pharmaceutical composition comprising:

(a) a synthetic miR-101 molecule comprising

i. an active strand comprising a sequence identical to human miR-101; and

ii. a separate complementary strand that is at least 60% complementary to the active strand and has a 5′-terminal nucleotide that is chemically modified to comprise a lower alkylamine group; and

(b) a pharmaceutically acceptable delivery vehicle.

6. The pharmaceutical composition of claim 5 , where the lower alkylamine group is attached to a 5′ phosphate of the 5′-terminal nucleotide of the complementary strand.

7. The pharmaceutical composition of claim 5 , wherein the active strand is 22-30 nucleotides in length.

8. The pharmaceutical composition of claim 5 , where the active strand is 23 nucleotides in length.

9. The pharmaceutical composition of claim 5 , wherein the delivery vehicle comprises a liposome.

10. The pharmaceutical composition of claim 5 , wherein the composition is suitable for intravenous administration to a subject.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 13, 2015
From: BROWN, DAVID; FORD, LANCE; CHENG, ANGIE; JARVIS, RICH; BYROM, MIKE; OVCHARENKO, DMITRIY; DEVROE, ERIC; KELNAR, KEVIN
To: AMBION, INC.
Reel/Frame 035631/0268 →
MERGER Recorded May 13, 2015
From: AMBION, INC.
To: APPLERA CORPORATION
Reel/Frame 035631/0500 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 13, 2015
From: APPLERA CORPORATION
To: ASURAGEN, INC.
Reel/Frame 035631/0703 →
Continuity (6)
Division 13190232 · Jul 25, 2011
Division 11273640 · Nov 14, 2005
Provisional Application 60683736 · May 23, 2005
Provisional Application 60649634 · Feb 3, 2005
Provisional Application 60627171 · Nov 12, 2004
Related Publication 20150004221A1 · Jan 1, 2015