Asgpr-binding compounds for the degradation of extracellular proteins
US-2024424108-A1 · Dec 26, 2024 · US
US9683017B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9683017-B2 |
| Application number | US-201514801717-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 16, 2015 |
| Priority date | Jul 17, 2014 |
| Publication date | Jun 20, 2017 |
| Grant date | Jun 20, 2017 |
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Disclosed are methods of treating and/or inhibiting a viral infection in a subject. The methods include administering a therapeutically effective amount of heparin-binding peptide. Also disclosed herein are methods for blocking viral binding to a cell. Further disclosed are anti-viral compositions for administration to a subject infected with a virus. Administration of the anti-viral composition inhibits viral infection of the subject.
Opening claim text (preview).
We claim: 1. A method for reducing a viral infection in a subject, comprising: selecting a subject in whom the viral infection is to be reduced; and administering to the subject an effective amount of a heparin-binding peptide comprising an amino acid sequence at least 95% identical to the amino acid sequence set forth as any one of SEQ ID NOs: 1-10, thereby reducing the viral infection in the subject. 2. The method of claim 1 , wherein the virus is an enveloped DNA virus or enveloped RNA virus. 3. The method of claim 1 , wherein the virus is a herpesvirus. 4. The method of claim 3 , wherein the herpesvirus is HSV-1. 5. The method of claim 3 , wherein the herpesvirus is cytomegalovirus (CMV). 6. The method of claim 1 , wherein the virus is human immunodeficiency virus (HIV). 7. A method for reducing binding of a virus to a cell, comprising: contacting a cell with an effective amount of a heparin-binding peptide, the heparin-binding peptide comprising an amino acid sequence at least 95% identical to the amino acid sequence set forth as any one of SEQ ID NOs: 1-10. 8. The method of claim 7 , wherein the virus is an enveloped DNA virus or enveloped RNA virus. 9. The method of claim 7 , wherein the virus is a herpesvirus. 10. The method of claim 9 , wherein the herpesvirus is HSV-1. 11. The method of claim 10 , wherein the herpesvirus is cytomegalovirus (CMV). 12. The method of claim 7 , wherein the virus is human immunodeficiency virus (HIV). 13. The method of claim 7 , wherein the heparin-binding peptide set forth as any one of SEQ ID NOs: 1-10 is a D-form peptide. 14. The method of claim 13 , wherein the D-form of the heparin-binding peptide comprises an amino acid sequence at least 95% identical to the amino acid sequence set forth as SEQ ID NO: 6. 15. The method of claim 7 , wherein contacting the cell with the effective amount of a heparin-binding peptide reduces viral infection of the cell. 16. An anti-viral composition, the composition comprising: a heparin-binding peptide, the heparin-binding peptide comprising an amino acid sequence at least 95% identical to the amino acid sequence set forth as any one of SEQ ID Nos. 3-10. 17. The anti-viral composition of claim 16 , wherein the heparin-binding peptide is present in an effective amount to reduce viral infection in a subject infected with a virus by at least 60%. 18. The anti-viral composition of claim 16 , wherein the heparin-binding peptide is present in an effective amount to reduce herpesvirus infection in a subject infected with herpesvirus. 19. The anti-viral composition of claim 16 , wherein the heparin-binding peptide is present in an effective amount to reduce cytomegalovirus infection in a subject infected with cytomegalovirus. 20. The anti-viral composition of claim 16 , wherein the heparin-binding peptide is present in an effective amount to reduce human immunodeficiency virus (HIV) infection in a subject infected with HIV.
having 12 to 20 amino acids (gastrins C07K14/595; somatostatins C07K14/655; melanotropins C07K14/68) · CPC title
Cytomegalovirus · CPC title
Herpes simplex virus I or II · CPC title
Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof {(enzyme inhibitors A61K38/005)} · CPC title
by chemical synthesis · CPC title
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