IP Library › Granted Patent US 7,745,390
Granted Patent B2
US 7,745,390 · App. 11/438,563 · Granted Jun 29, 2010

Antimicrobial peptides

Assignee: The Board of Trustees of the Leland Stanford Junior University
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Quick Facts
Patent No.
US 7,745,390
App. No.
11/438,563
Granted
Jun 29, 2010
Kind
B2
Abstract

Artificial antimicrobial peptides are obtained by alterations in alpha helical portions of a known antimicrobial protein, granulysin. The peptides obtained have significantly improved antimicrobial activity and lack the ability to lyse mammalian cells, which may be toxic to a host. The peptides may be designed according to certain guidelines, and may further be modified by the addition of altered residues and alterations in normal peptide secondary and tertiary structure, including modifications in quaternary (multimeric) structure.

Claims (31)

1. An artificial antimicrobial peptide having:

at least 90% sequence identity to peptide G11.46 (SEQ ID NO: 93), G12.21 (SEQ ID NO: 64) or G14.15 (SEQ ID NO: 83), but further having at least one non-identical amino acid when compared to SEQ ID NO: 2, an MIC against at least one of a pathogenic bacterium selected from the group consisting of E. coli, S. typhimurium and B. cereus of less than 10 μM; and

having minimal lytic activity against mammalian cells.

2. The artificial antimicrobial peptide of claim 1 further comprised in a pharmaceutically acceptable composition.

3. The pharmaceutical preparation of claim 2 further comprising a sterile lyophilized powder.

4. The artificial antimicrobial peptide of claim 1 having a net positive charge of at least 8.

5. The artificial peptide of claim 1 having more D-amino acids than L-amino acids.

6. The artificial peptide of claim 1 having at least 3 hydrophobic residues.

7. An artificial antimicrobial peptide selected from the group consisting of:

G8.17, (SEQ ID NO: 9), G8.3, (SEQ ID NO: 12), G8.15, (SEQ ID NO: 13), G8.11, (SEQ ID NO: 18), G11.6, (SEQ ID NO: 16), G11.3, (SEQ ID NO: 26), G11.24, (SEQ ID NO: 26), G11.30, (SEQ ID NO: 39), G11.32, (SEQ ID NO: 41), G11.34, (SEQ ID NO: 26), G11.35, (SEQ ID NO: 48), G11.55, (SEQ ID NO: 35), G11.46, (SEQ ID NO: 93), G12.5, (SEQ ID NO: 51), G12.10, (SEQ ID NO: 61), G12.19, (SEQ ID NO: 65), G12.20, (SEQ ID NO: 66), G12.21, (SEQ ID NO: 64), G14.2, (SEQ ID NO: 81), G14.10, (SEQ ID NO: 81), G14.11, (SEQ ID NO: 83), and G14.15 (SEQ ID NO: 83), wherein said peptide has an MIC (μM) in at least two microbial organisms selected from the group consisting of: E. coli, S. typhimurium, V. cholerae and B. cereus of less than about 2.0, and further has minimal lysis of mammalian cells.

8. The peptide of claim 7 wherein said peptide is selected from: G8.3, (SEQ ID NO: 12), G8.15, (SEQ ID NO: 13), G 8.11, (SEQ ID NO: 18), G11.46, (SEQ ID NO: 93), G12.21 (SEQ ID NO: 64), and G14.15 (SEQ ID NO: 83).

9. The peptide of claim 7 selected from the group consisting of G11.46, (SEQ ID NO: 93), G12.21 (SEQ ID NO: 64), and G14.15 (SEQ ID NO: 83).

10. The peptide of claim 7 comprising at least 50% D-amino acids.

11. The peptide of claim 7 comprising the sequence arg-arg-val-ser-arg-arg (SEQ ID NO: 92).

12. The peptide of claim 7 comprising at least 50% D-amino acids.

13. The peptide of claim 7 comprising the sequence arg-arg-val-ser-arg-arg (SEQ ID NO: 92).

14. A method of inhibiting microbial growth in an infected subject, comprising administering to said subject a composition comprising a peptide having a formula according to claim 7 .

15. A method of inhibiting microbial growth in an infected subject, comprising administering to said subject a composition comprising a peptide having a formula according to claim 4 .

16. A method for treating bacterial or fungal infection, comprising administering to a living body in need of such treatment a therapeutically effective amount of a peptide according to claim 1 .

17. A method for preparing an antimicrobial peptide, comprising:

(a) selecting a sequence of between 10 and 20 residues comprised in SEQ ID NO: 2;

(b) modifying the sequence by increasing a selected number of charged residues to be at least 8 residues;

(c) modifying the sequence to include at least one D-amino acid;

(d) preparing the peptide;

(e) testing the peptide for antimicrobial activity against at least 3 microorganisms and selecting only a peptide with an MIC less than 1.0 μM against at least one of the microorganisms, and selecting as the antimicrobial peptide one having at least 90% sequence identity to peptide G11.46, (SEQ ID NO: 93), G12.21 (SEQ ID NO: 64), or 90% sequence identity to G14.15 (SEQ ID NO: 83), having at least one non-identical amino acid when compared to SEQ ID NO: 2 and having minimum lytic activity against mammalian cells.

18. The method of claim 17 further comprising the step of preparing a dendrimer containing the peptide.

19. The method of claim 17 further comprising the step of including at least one chemically modified amino acid.

20. The peptide of claim 1 further comprised in a dendrimer.

21. The peptide of claim 1 comprising at least 7 arg residues.

22. The peptide of claim 1 further comprising at least one chemically modified amino acid.

23. The peptide of claim 1 wherein the MIC against at least one of a pathogenic bacterium is less than 1 μM.

Assignments (2)
EXECUTIVE ORDER 9424, CONFIRMATORY LICENSE Recorded Nov 17, 2008
From: STANFORD UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 021843/0546 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 1, 2006
From: CLAYBERGER, CAROL; KRENSKY, ALAN M.
To: THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
Reel/Frame 017708/0236 →
Continuity (2)
Provisional Application 6068403200 · May 23, 2005
Related Publication 20060287232A1 · Dec 21, 2006