Cripto mutant and uses thereof
View Patent ↗The present invention is based on the discovery that CRIPTO mutants each comprising at least one amino acid substitution from a CRIPTO polypeptide demonstrate tumor blocking activity.
1. An in vitro method for inhibiting fucosylation-dependent signaling of the CRIPTO polypeptide shown in SEQ ID NO:1 in a tumor cell that expresses said CRIPTO polypeptide, comprising exposing said tumor cell to an effective amount of the CRIPTO polypeptide shown in SEQ ID NO: 1 in which from one to three amino acids are substituted with a different replacement amino acid to form a mutant CRIPTO polypeptide, wherein the position of the from one to three amino acid substitutions are selected from the group consisting of amino acid residues 86, 87 and 88 of the CRIPTO polypeptide.
2. The method of claim 1 , wherein the replacement amino acids are selected from the group consisting of an alanine or a glycine.
3. The method of claim 1 , wherein the mutant CRIPTO polypeptide comprises an amino acid substitution at position 86.
4. The method of claim 1 , wherein the mutant CRIPTO polypeptide comprises an amino acid substitution at position 87.
5. The method of claim 1 , wherein the mutant CRIPTO polypeptide comprises an amino acid substitution at position 88.
6. The method of any one of claims 3 - 5 , wherein the replacement amino acid is an alanine or a glycine.
7. An in vitro method for inhibiting fucosylation-dependent signaling of the CRIPTO polypeptide shown in SEQ ID NO:1 in a tumor cell that expresses said CRIPTO polypeptide, comprising exposing said tumor cell to an effective amount of a mutant CRIPTO polypeptide, wherein the mutant CRIPTO polypeptide is encoded by a nucleic acid molecule which hybridizes over its full length to the complement of the nucleic acid molecule of SEQ ID NO:36 (CR-1) under conditions of 68° C. in 5×SSC/5× Denhardt's solution/1.0% SDS followed by washing in 0.2×SSC/0.1% SDS at room temperature, and wherein said mutant CRIPTO polypeptide comprises from one to three amino acid substitutions, wherein the position of the from one to three amino acid substitutions are selected from the group consisting of amino acid residues 86, 87, and 88 of the CRIPTO polypeptide.