IP Library Granted Patent US 7,018,984
Granted Patent B1
US 7,018,984 · App. 08/477,895 · Granted Mar 28, 2006

Methods and compositions for controlling translation of HCV proteins

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Quick Facts
Patent No.
US 7,018,984
App. No.
08/477,895
Granted
Mar 28, 2006
Kind
B1
Abstract

Embodiments of the present invention feature methods and compositions for controlling the translation of viral peptides and proteins from viral nucleic acid, with particular applications to pestivirus and HCV. The methods and compositions feature control elements of the 5′UT region of the viral genome.

Claims (12)

1. A method of controlling translation of hepatitis C virus (HCV) proteins from HCV nucleic acid comprising the steps:

providing a non-naturally occurring first nucleic acid which first nucleic acid comprises a sequence having ten or more nucleotides complementary to a sense strand within the 5′ UT region of HCV nucleic acid, wherein said first nucleic acid hybridizes to bases 1–23 of (SEQ ID NO: 1); and

contacting said HCV nucleic acid with said first nucleic acid under conditions where said first nucleic acid and HCV nucleic acid form a hybridization product, whereby translation of the HCV nucleic acid is altered.

2. A method of controlling translation of hepatitis C virus (HCV) proteins from HCV nucleic acid comprising the steps:

providing a non-naturally occurring first nucleic acid which first nucleic acid comprises a sequence having ten or more nucleotides complementary to a sense strand within the 5′ UT region of HCV nucleic acid, wherein said first nucleic acid hybridizes to bases 277–300 of (SEQ ID NO: 1); and

contacting said HCV nucleic acid with said first nucleic acid under conditions where said first nucleic acid and HCV nucleic acid form a hybridization product, whereby translation of the HCV nucleic acid is altered.

3. The method of claim 2 wherein said first nucleic acid is a phosphorothioate nucleic acid analog.

4. A method of controlling the translation of hepatitis C virus (HCV) proteins from HCV nucleic acid comprising the steps:

providing a non-naturally occurring first nucleic acid which first nucleic acid comprises a sequence having ten or more nucleotides complementary to a sense strand within the 5′UT region of HCV nucleic acid, wherein said first nucleic acid comprises a sequence selected from the group consisting of a hairpin-forming region, a pestivirus homology box IV area, and a cleavage area at which the full length HCV RNA is cleaved to form a subgenomic HCV RNA;

contacting said HCV nucleic acid with said first nucleic acid under conditions where said first nucleic acid and HCV nucleic acid form a hybridization product, whereby translation of the HCV nucleic acid is altered; and transcribing a non-naturally occurring second nucleic acid comprising a promoter operatively linked to a sequence complementary to said first nucleic acid.

5. The method of claim 4 wherein said second nucleic acid and promoter are placed in a cell infected with HCV, which cell transcribes said second nucleic acid.

6. The method of claim 3 wherein said first nucleic acid further comprises a cholesteryl moiety linked at the 3′ end.

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE AND ASSIGNOR. PREVIOUSLY RECORDED ON REEL 033886 FRAME 0313. ASSIGNOR(S) HEREBY CONFIRMS THE CONFIRMATORY ASSIGNMENT. Recorded Oct 20, 2014
From: NOVARTIS VACCINES AND DIAGNOSTICS, INC.
To: NOVARTIS VACCINES AND DIAGNOSTICS, INC.; GRIFOLS WORLDWIDE OPERATIONS LIMITED
Reel/Frame 034116/0974 →
CONFIRMATORY ASSIGNMENT Recorded Oct 2, 2014
From: NOVARTIS VACCINES AND DIAGNOSTICS, INC.; NOVARTIS AG
To: NOVARTIS VACCINES AND DIAGNOSTICS, INC.; NOVARTIS AG; GRIFOLS WORLDWIDE OPERATIONS LIMITED
Reel/Frame 033886/0313 →