IP Library Granted Patent US 11,912,794
Granted Patent B2
US 11,912,794 · App. 16/899,192 · Granted Feb 27, 2024

Modulation of structured polypeptide specificity

Inventors: John Tite (Cambridge, GB); Edward Walker (Cambridge, GB); Catherine Stace (Cambridge, GB); Daniel Teufel (Cambridge, GB)
Assignee: BicycleRD Limited
C07K7/56A61K38/10A61K38/12C07K1/00C07K1/1075C07K2/00C07K7/08C07K7/64
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Quick Facts
Patent No.
US 11,912,794
App. No.
16/899,192
Granted
Feb 27, 2024
Kind
B2
Abstract

The invention describes peptide ligands specific for human plasma Kallikrein.

Claims (22)

1. A peptide ligand specific for human kallikrein comprising a polypeptide comprising at least three cysteine residues, separated by at least two loop sequences, and a molecular scaffold which forms covalent bonds with the cysteine residues of the polypeptide such that at least two polypeptide loops are formed on the molecular scaffold, wherein the loops of the peptide ligand comprise five amino acids and a first loop comprises the motif G r x W / F PX K / R G r (SEQ ID NO: 209), a second loop comprises the motif G r xHXDLG r (SEQ ID NO: 210) and wherein the first G r of the second loop is the second G r of the first loop, wherein G r represents cysteine and x represents any amino acid, and wherein R may optionally be replaced with N-methyl arginine, homoarginine or guanidylphenylalanine, and/or P may optionally be replaced with azetidine carboxylic acid.

2. The peptide ligand according to claim 1 , wherein the first loop comprises the sequence selected from G r xWPARG r (SEQ ID NO: 4), G r xWPSRG r (SEQ ID NO: 5), G r xFPFRG r (SEQ ID NO: 6), and G r xFPYRG r (SEQ ID NO: 7), wherein G r represents cysteine and x represents any amino acid.

3. The peptide ligand according to claim 2 , wherein x is S or R.

4. The peptide ligand according to claim 1 , wherein R is replaced with N-methyl arginine.

5. The peptide ligand according to claim 1 , wherein R is replaced with homoarginine.

6. The peptide ligand according to claim 1 , wherein R is replaced with guanidylphenylalanine.

7. The peptide ligand according to claim 1 , wherein P is replaced with azetidine carboxylic acid.

8. The peptide ligand according to claim 1 , wherein x at position 2 of SEQ ID NO: 209 is S or R.

9. The peptide ligand according to claim 1 , wherein the polypeptide comprises two adjacent loops which comprise the motif G r x W / F PX K / R G r xHxDLG r (SEQ ID NO: 211).

10. The peptide ligand according to claim 1 , wherein the molecular scaffold comprises reactive groups for forming covalent bonds with the cysteine residues of the polypeptide, wherein the reactive groups are selected from the group consisting of alkyl halides and maleimides.

11. The peptide ligand according to claim 10 , wherein the molecular scaffold is a tris(bromomethyl)benzene, or a derivative thereof.

12. The peptide ligand according to claim 11 , wherein the molecular scaffold is 1,3,5-Tris(bromomethyl)-2,4,6-trimethylbenzene, 1,3,5-Tris(bromomethyl)benzene, or 1,3,5-Tris(bromomethyl)-2,4,6-triethylbenzene.

13. The peptide ligand according to claim 12 , wherein the molecular scaffold is 1,3,5-Tris(bromomethyl)benzene.

14. The peptide ligand according to claim 10 , wherein the molecular scaffold is tris-(2-maleimidoethyl)amine, tris-(2-maleimidoethyl)benzene, or tris-(maleimido)benzene.

15. The peptide ligand according to claim 1 , wherein the peptide ligand is attached to an antibody or a fragment thereof.

16. The peptide ligand according to claim 15 , wherein:

the antibody fragment is selected from an antibody light chain constant region (CL), an antibody CH1 heavy chain domain, an antibody CH2 heavy chain domain, an antibody CH3 heavy chain domain, or any combination thereof, in addition to the one or more constant region domains; or

the antibody fragment comprises a hinge region of an antibody; or

the antibody fragment comprises an Fc region of an IgG molecule.

17. The peptide ligand according to claim 16 , wherein the hinge region comprises the region between the CH1 and CH2 domains of an IgG molecule.

18. The peptide ligand according to claim 9 , wherein the polypeptide comprises two adjacent loops which comprise the motif G r SFPYRG r xHQDLG r (SEQ ID NO: 212), wherein x represents any amino acid, and wherein R is replaced with N-methyl arginine; or R is replaced with homoarginine, or R is replaced with guanidylphenylalanine, and/or wherein P is replaced with azetidine carboxylic acid.

19. A pharmaceutical composition comprising the peptide ligand according to claim 1 , and a pharmacologically appropriate carrier.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 21, 2020
From: TITE, JOHN; WALKER, EDWARD; STACE, CATHERINE; TEUFEL, DANIEL
To: BICYCLE THERAPEUTICS LIMITED
Reel/Frame 053264/0691 →
CHANGE OF NAME Recorded Jul 21, 2020
From: BICYCLE THERAPEUTICS LIMITED
To: BICYCLERD LIMITED
Reel/Frame 053264/0842 →
Priority Claims (2)
GB 1117408 · Oct 7, 2011 · national
GB 1205612 · Mar 29, 2012 · national
Continuity (2)
Continuation 14350192
Related Publication 20210122786A1 · Apr 29, 2021