IP Library Granted Patent US 7,632,801
Granted Patent B2
US 7,632,801 · App. 10/337,213 · Granted Dec 15, 2009

Identification and use of antiviral compounds that inhibit interaction of host cell proteins and viral proteins required for viral replication

Assignee: Mount Sinai School of Medicine of New York University
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Quick Facts
Patent No.
US 7,632,801
App. No.
10/337,213
Granted
Dec 15, 2009
Kind
B2
Abstract

The present invention relates to the identification of host cell proteins that interact with viral proteins required for virus replication, and high throughput assays to identify compounds that interfere with the specific interaction between the viral and host cell protein. Interfering compounds that inhibit viral replication can be used therapeutically to treat viral infection. The invention is based, in part, on the Applicants' discovery of novel interactions between viral proteins and a human host cell proteins. One of these host cell proteins, referred to herein as NPI-1, interacts with influenza virus protein NP. Also, host cell proteins, referred to herein as NS1I-1 and NS1-BP interact with influenza virus protein NS 1 . In addition, host cell proteins containing WW domains that interact with viral proteins such as Rhabdoviral M protein are described. Compounds that interfere with the binding of the host cell and viral proteins, and inhibit viral replication can be useful for treating viral infection in vivo.

Claims (18)

1. A method for inhibiting or reducing influenza A virus growth, comprising contacting a first composition comprising a cell and an influenza A virus with a second composition comprising a compound that inhibits or reduces the interaction between amino acid residues 2 to 20 of an influenza A virus nucleoprotein (NP) and nucleoprotein interactor 1 (NPI-1), wherein the compound is a polypeptide which comprises the amino acid sequence of the formula Ala Xaa 2 Xaa 3 Gly Thr Lys Arg Xaa 8 Tyr Xaa 10 Gln Met Glu Thr Xaa 15 Gly Xaa 17 Arg Xaa 19 (SEQ ID NO: 44) or Xaa 2 Xaa 3 Gly Thr Lys Arg Xaa 8 Tyr Xaa 10 Gln Met (SEQ ID NO: 45), wherein Xaa 2 is Ser or Thr, Xaa 3 is Gln or Lys, Xaa 8 is Ser or Pro, Xaa 10 is Glu or Gly, Xaa 15 is Asp or Gly, Xaa 17 is Glu or Asp, and Xaa 19 is Gln or is absent.

2. The method of claim 1 , wherein the polypeptide comprises the amino acid sequence Ala Ser Gln Gly Thr Lys Arg Ser Tyr Glu Gln Met Glu Thr Asp Gly Glu Arg Gln (SEQ ID NO: 22).

3. The method of claim 1 , wherein the polypeptide comprises the amino acid sequence of the formula Xaa 2 Xaa 3 Gly Thr Lys Arg Xaa 8 Tyr Xaa 10 Gln Met (SEQ ID NO: 45).

4. The method of claim 1 , wherein the polypeptide comprises the amino acid sequence of the formula Ala Xaa 2 Xaa 3 Gly Thr Lys Arg Xaa 8 Tyr Xaa 10 Gln Met Glu Thr Xaa 15 Gly Xaa 17 Arg Xaa 19 (SEQ ID NO: 44).

5. A method for inhibiting or reducing influenza A virus growth, comprising contacting a first composition comprising) a cell and an influenza A virus with a second con position comprising a compound that inhibits or reduces the interaction between amino acid residues 2 to 20 of an influenza A virus nucleoprotein (NP) and nucleoprotein interactor 1 (NPI-1), wherein the compound is a polypeptide which comprises the amino acid sequence of the formula Ser Xaa 2 Gly Thr Lys Arg Ser Tyr Xaa 9 Xaa 10 Met (SEQ ID NO: 40).

6. The method of claim 5 , wherein the polypeptide comprises the amino acid sequence Ser Gln Gly Thr Lys Arg Ser Tyr Glu Gln Met (SEQ ID NO: 46).

7. A method for inhibiting or reducing an influenza A virus infection, comprising administering to an animal in need thereof a therapeutically effective amount of a composition comprising a polypeptide that inhibits the interaction of an influenza A virus nucleoprotein (NP) and nucleoprotein interactor 1 (NPI-1), wherein the polypeptide comprises the amino acid sequence of the formula Ala Xaa 2 Xaa 3 Gly Thr Lys Arg Xaa 8 Tyr Xaa 10 Gln Met Glu Thr Xaa 15 Gly Xaa 17 Arg Xaa 19 (SEQ ID NO: 44) or Xaa 2 Xaa 3 Gly Thr Lys Arg Xaa 8 Try Xaa 10 Gln Met (SEQ ID NO: 45), wherein Xaa 2 is Ser or Thr, Xaa 3 is Gln or Lys, Xaa 8 is Ser or Pro, Xaa 10 is Glu or Gly, Xaa 15 is Asp or Gly, Xaa 17 is Glu or Asp, and Xaa 19 is Gln or is absent.

8. The method of claim 7 , wherein the polypeptide comprises the amino acid sequence of the formula Ala Xaa 2 Xaa 3 Gly Thr Lys Arg Xaa 8 Tyr Xaa 10 Gln Met Glu Thr Xaa 15 Gly Xaa 17 Arg Xaa 19 (SEQ ID NO: 44).

9. The method of claim 8 , wherein the polypeptide comprises the amino acid sequence Ala Ser Gln Gly Thr Lys Arg Ser Tyr Glu Gln Met Glu Thr Asp Gly Glu Arg Gln (SEQ ID NO: 22).

10. The method of claim 7 , wherein the animal is a human.

11. The method of claim 7 , wherein the polypeptide comprises the amino acid sequence of the formula Xaa 2 Xaa 3 Gly Thr Lys Arg Xaa 8 Tyr Xaa 10 Gln Met (SEQ ID NO: 45).

12. The method of claim 7 , wherein the composition is administered intranasally, orally, or intramuscularly.

13. A method for inhibiting or reducing an influenza A virus infection, comprising administering to an animal in need thereof a therapeutically effective amount of a composition comprising a polypeptide that inhibits the interaction of an influenza A virus nucleoprotein (NP) and nucleoprotein interactor 1 (NPI-1), wherein the polypeptide comprises the amino acid sequence of the formula Ser Xaa 2 Gly Thr Lys Arg Ser Tyr Xaa 9 Xaa 10 Met (SEQ ID NO: 40).

14. The method of claim 13 , wherein the polypeptide comprises the amino acid sequence Ser Gln Gly Thr Lys Arg Ser Tyr Glu Gln Met (SEQ ID NO: 46).

15. The method of claim 13 , wherein the animal is a human.

16. The method of claim 13 , wherein the composition is administered intranasally, orally, or intramuscularly.

17. The method of claim 9 or 14 , wherein the animal is a human.

18. The method of claim 9 or 14 , wherein the composition is administered intranasally, orally, or intramuscularly.

Assignments (1)
CONFIRMATORY LICENSE Recorded Jun 9, 2016
From: ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 038926/0544 →
Continuity (4)
Division 0963679100 · Aug 11, 2000
Continuation In Part 0844499400 · May 19, 1995
Provisional Application 6014826300 · Aug 11, 1999
Related Publication 20030232325A1 · Dec 18, 2003