IP Library Granted Patent US 8,614,069
Granted Patent B2
US 8,614,069 · App. 13/059,695 · Granted Dec 24, 2013

Non-cytotoxic fusion proteins comprising EGF muteins

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Quick Facts
Patent No.
US 8,614,069
App. No.
13/059,695
Granted
Dec 24, 2013
Kind
B2
Abstract

The present invention relates to fusion proteins comprising a non-cytotoxic protease and a EGF mutein ligand. The EGF mutein provides improved EGF receptor activation for the claimed fusion proteins. Also provided is the use of said polypeptides as therapeutics for suppressing mucus hypersecretion, inflammation, endocrine neoplasia and/or neuroendocrine disorders, neuroendocrine tumors, for suppressing cancers such as colorectal cancer, prostate cancer, breast cancer, and lung cancer.

Claims (12)

1. A polypeptide, comprising:

a) a non-cytotoxic protease selected from the group consisting of Clostridial neurotoxin protease and Neisseria IgA protease, wherein the non-cytotoxic protease is capable of cleaving a SNARE, protein;

b) a translocation peptide that is capable of translocating said non-cytotoxic protease from within an endosome of a mammalian cell, across the endosomal membrane thereof and into the cytosol of the mammalian cell, wherein the translocation peptide is selected from the group consisting of: a clostridial neurotoxin translocation domain selected from the group consisting of Botulinum Type A, B, C, D, F, F and G neurotoxin translocation domain and tetanus neurotoxin translocation domain, diphtheria toxin translocation domain, Pseudomonas exotoxin type A translocation domain, Anthrax toxin translocation domain, Influenza Virus haemagglutinin translocation domain, Semliki Forest Virus fusogenic protein translocation domain, Semliki Forest Virus E1 protein translocation domain, Vesicular Stomatitis Virus glycoprotein G translocation domain, SER Virus F protein translocation domain, and Foamy Virus envelope glycoprotein translocation domain; and

c) an epidermal growth factor (EGF) mutein, wherein said EGF mutein comprises an amino acid sequence having at least 95% sequence identity to the amino acid sequence of SEQ ID NO: 11, and wherein said EGF mutein retains the binding ability of SEQ ID NO: 11 to bind to an EGF receptor.

2. A polypeptide comprising an amino acid sequence having at least 95% sequence identity to an amino acid sequence selected from the group consisting of SEQ ID NOs: 37, 64, 66 and 68;

wherein the amino acid sequence comprises:

a non-cytotoxic protease that is capable of cleaving a snare protein;

a translocation peptide that is capable of translocating the non-cytotoxic protease from within an endosome of a mammalian cell, across the endosomal membrane thereof and into the cytosol of the mammalian cell; and

a targeting moiety which is capable of binding to EGF receptor.

3. The polypeptide according to claim 1 , wherein the translocation peptide comprises a clostridial neurotoxin translocation domain.

4. The polypeptide according to claim 1 , wherein the polypeptide is present as a di-chain polypeptide, wherein the non-cytotoxic protease is linked to the translocation peptide by a disulphide bond.

5. The polypeptide according to claim 1 , wherein the polypeptide is an isolated or recombinant polypeptide.

Assignments (2)
CHANGE OF NAME AND ADDRESS Recorded May 15, 2017
From: SYNTAXIN LIMITED
To: IPSEN BIOINNOVATION LIMITED
Reel/Frame 042458/0982 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 30, 2011
From: COSSINS, AIMEE; BIRCH-MACHIN, IAN; STANCOMBE, PATRICK
To: SYNTAXIN LIMITED
Reel/Frame 026047/0754 →