IP Library Granted Patent US 9,464,125
Granted Patent B2
US 9,464,125 · App. 14/376,223 · Granted Oct 11, 2016

Engineered potent cytotoxic stapled BH3 peptides

Inventors: A. James Link (Princeton, NJ); Siyan Zhang (Plainsboro, NJ)
Assignee: The Trustees of Princeton University
C07K14/4747A61K38/00A61K38/10A61K38/12A61K38/1761C07K7/08
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Quick Facts
Patent No.
US 9,464,125
App. No.
14/376,223
Granted
Oct 11, 2016
Kind
B2
Abstract

Compositions comprising peptide sequences with high cytotoxicity to cancer cell lines are provided. Pharmaceutical compositions comprising peptide sequences with high cytotoxicity to cancer cell lines are provided. A method for treating cancer is provided.

Claims (14)

1. A composition comprising an engineered cytotoxic stapled BH3 peptide comprising a fourteen amino acid sequence having the sequence of one of Trp-Val-Ala-Gln-Trp-Leu-Arg-Arg-Trp-Gly-Asp-Glu-Phe-Asn (SEQ ID NO: 2); Trp-Tyr-Ala-Gln-Ile-Leu-Arg-Arg-Met-Gly-Asp-Glu-Phe-Asn (SEQ ID NO: 3); Trp-Leu-Ala-Gln-Leu-Leu-Arg-Arg-Tyr-Gly-Asp-Glu-Phe-Asn (SEQ ID NO: 4); Trp-Ile-Ala-Gln-Ile-Leu-Arg-Arg-Trp-Gly-Asp-Glu-Phe-Asn (SEQ ID NO: 5); Trp-Val-Ala-Gln-Thr-Leu-Arg-Arg-Trp-Gly-Asp-Glu-Phe-Asn (SEQ ID NO: 6); Trp-Ile-Ala-Gln-Leu-Leu-Arg-Arg-Ile-Gly-Asp-Glu-Val-Asn (SEQ ID NO: 7); Trp-Val-Ala-Gln-Leu-Leu-Arg-Arg-Ile-Gly-Asp-Glu-Val-Asn (SEQ ID NO: 8); Trp-Met-Ala-Gln-Ile-Leu-Arg-Arg-Ile-Gly-Asp-Glu-Val-Asn (SEQ ID NO: 9); Trp-Leu-Ala-Gln-Leu-Leu-Arg-Arg-Ile-Gly-Asp-Glu-Ile-Asn (SEQ ID NO: 10); or Trp-Leu-Ala-Gln-Glu-Leu-Arg-Arg-Ile-Gly-Asp-Glu-Val-Asn (SEQ ID NO: 11) and a crosslink, wherein the crosslink is from amino acid side chain to amino acid side chain within the fourteen amino acid sequence, from amino acid side chain to peptide backbone within the fourteen amino acid sequence, or between the Arg residue at position 8 of the fourteen amino acid sequence or a replacement thereof and the Glu residue at position 12 of the fourteen amino acid sequence or a replacement thereof.

2. The composition of claim 1 , wherein the engineered cytotoxic stapled BH3 peptide is 14, 15, or 16 amino acids in length.

3. The composition of claim 1 , wherein the crosslink is between the Arg residue at position 8 of the fourteen amino acid sequence or a replacement thereof and the Glu residue at position 12 of the fourteen amino acid sequence or a replacement thereof.

4. The composition of claim 1 further comprising at least one of ABT-737 or ABT-199.

5. The composition of claim 1 further comprising a pharmaceutically acceptable carrier.

6. The composition of claim 5 , wherein the pharmaceutically acceptable carrier includes at least one substance selected from the group consisting of ion exchangers; alumina; aluminum stearate; lecithin; serum proteins; human serum albumin; buffer substances; phosphates; glycine; sorbic acid; potassium sorbate; partial glyceride mixtures of saturated vegetable fatty acids; water; salts; electrolytes; protamine sulfate; disodium hydrogen phosphate; potassium hydrogen phosphate; sodium chloride; zinc salts; colloidal silica; magnesium trisilicate; polyvinyl pyrrolidone; cellulose-based substances; polyethylene glycol; sodium carboxymethylcellulose; waxes; polyethylene glycol; starch; lactose; dicalcium phosphate; microcrystalline cellulose; sucrose; dextrose; talc; magnesium carbonate; kaolin; non-ionic surfactants; edible oils; physiological saline; bacteriostatic water; and phosphate buffered saline (PBS).

7. A composition comprising an engineered cytotoxic stapled BH3 peptide having the structure of

wherein the Xaa-bracket-Xaa is a crosslink between an α,α-disubstituted 5-carbon olefinic unnatural amino acid at position 8 and an α,α-disubstituted 5-carbon olefinic unnatural amino acid at position 12.

8. The composition of claim 7 , wherein the engineered cytotoxic stapled BH3 peptide has the structure of Formula I:

9. The composition of claim 7 , wherein the engineered cytotoxic stapled BH3 peptide has the structure of Formula III:

10. The composition of claim 7 , wherein the engineered cytotoxic stapled BH3 peptide has the structure of Formula VII:

11. The composition of claim 7 , wherein the engineered cytotoxic stapled BH3 peptide has the structure of Formula IX:

12. The composition of claim 7 further comprising a pharmaceutically acceptable carrier.

13. The composition of claim 12 , wherein the pharmaceutically acceptable carrier includes at least one substance selected from the group consisting of ion exchangers; alumina; aluminum stearate; lecithin; serum proteins; human serum albumin; buffer substances; phosphates; glycine; sorbic acid; potassium sorbate; partial glyceride mixtures of saturated vegetable fatty acids; water; salts; electrolytes; protamine sulfate; disodium hydrogen phosphate; potassium hydrogen phosphate; sodium chloride; zinc salts; colloidal silica; magnesium trisilicate; polyvinyl pyrrolidone; cellulose-based substances; polyethylene glycol; sodium carboxymethylcellulose; waxes; polyethylene glycol; starch; lactose; dicalcium phosphate; microcrystalline cellulose; sucrose; dextrose; talc; magnesium carbonate; kaolin; non-ionic surfactants; edible oils; physiological saline; bacteriostatic water; and phosphate buffered saline (PBS).

Assignments (2)
CONFIRMATORY LICENSE Recorded Apr 10, 2015
From: PRINCETON UNIVERSITY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 035412/0851 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 29, 2014
From: LINK, A. JAMES; ZHANG, SIYAN
To: THE TRUSTEES OF PRINCETON UNIVERSITY
Reel/Frame 033841/0544 →
Continuity (2)
Provisional Application 61594810 · Feb 3, 2012
Related Publication 20150045310A1 · Feb 12, 2015