Asgpr-binding compounds for the degradation of extracellular proteins
US-2024424108-A1 · Dec 26, 2024 · US
US9518090B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9518090-B2 |
| Application number | US-201314431622-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 26, 2013 |
| Priority date | Sep 26, 2012 |
| Publication date | Dec 13, 2016 |
| Grant date | Dec 13, 2016 |
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The present invention provides compositions and methods for treating hepatitis B virus (HBV) infection as well as methods for identifying a compound or a composition that is suitable for treating HBV infection. In addition, the present invention provides a suitable non-mammalian animal model that can be used to screen for a compound or a composition that can inhibit HBV replication or treat HBV infection in a mammal. In particular, the present invention provides compositions and methods for treating hepatitis B infection by inhibiting interaction between HBV x protein and a Bcl-2 family protein or by reducing the expression level of a Bcl-2 family protein.
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What is claimed is: 1. A method for treating hepatitis B infection in a subject, said method comprising administering to a subject in need of such a treatment a composition (i) that is capable of inhibiting binding of hepatitis B virus X protein to a Bcl-2 family member protein in said subject; (ii) that is capable of reducing the expression of Bcl-2family member protein in said subject; or (iii) a combination thereof. 2. The method of claim 1 , wherein said Blc-2 family member protein comprises Bcl-2, Bcl-xL, or a combination thereof. 3. The method of claim 1 , wherein said composition comprises a binding inhibitor that is capable of inhibiting binding of hepatitis B virus X protein to said Bcl-2 family member protein. 4. The method of claim 3 , wherein said binding inhibitor is capable of interacting with Bcl-2 homology 3 (BH3)-like motif of hepatitis B virus X protein or a Bcl-2 family member. 5. The method of claim 1 , wherein said composition comprises an expression inhibitor that is capable of reducing the expression of Bcl-2 family member protein. 6. The method of claim 5 , wherein said expression inhibitor is a siRNA or a small RNA that is capable of reducing the expression of Bcl-2, Bcl-xL, or a combination thereof. 7. A method for identifying a composition that is capable of treating hepatitis B virus (HBV) infection in a mammal, said method comprising determining the effect of said composition in an interaction between HBV X protein and CED-9 protein of C. elegans, wherein modulation of the interaction between HBV X protein and CED-9 protein in the presence of said composition is an indication that said composition is capable of treating HBV infection in a mammal. 8. A method for treating hepatitis B infection in a subject, said method comprising administering to a subject in need of such a treatment a therapeutically effective amount of a composition comprising peptaibol TK. 9. The method of claim 8 , wherein said peptaibol TK comprises peptaibol TK VI (SEQ ID NO: 1), peptaibol TK VII (SEQ ID NO: 2), peptaibol TK VIII (SEQ ID NO: 3) or a mixture thereof.
for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics · CPC title
Screening involving studying the effect of compounds C on the interaction between interacting molecules A and B (e.g. A = enzyme and B = substrate for A, or A = receptor and B = ligand for the receptor) · CPC title
against oncogenes or tumor suppressor genes · CPC title
involving cells · CPC title
Medicinal preparations containing peptides (peptides containing beta-lactam rings A61K31/00; cyclic dipeptides not having in their molecule any other peptide link than those which form their ring, e.g. piperazine-2,5-diones, A61K31/00; ergot alkaloids of the cyclic peptide type A61K31/48; containing macromolecular compounds having statistically distributed amino acid units A61K31/74; medicinal preparations containing antigens or antibodies A61K39/00; medicinal preparations characterised by the non-active ingredients, e.g. peptides as drug carriers, A61K47/00) · CPC title
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