Fusion constructs and use of same to produce antibodies with increased Fc receptor binding affinity and effector function
The present invention relates to the field of glycosylation engineering of proteins. More particularly, the present invention relates to nucleic acid molecules, including fusion constructs, having catalytic activity and the use of same in glycosylation engineering of host cells to generate polypeptides with improved therapeutic properties, including antibodies with increased Fc receptor binding and increased effector function.
1. A method for modifying the glycosylation profile of a polypeptide produced by a mammalian host cell, comprising introducing into said host cell an isolated nucleic acid comprising a sequence encoding a fusion polypeptide, wherein said fusion polypeptide has β(1,4)-N-acetylglucosaminyltransferase III activity and comprises the Golgi localization domain of mannosidase II, and wherein said modified polypeptide has increased Fc-receptor binding or effector function as a result of said modification.
2. A method for modifying the glycosylation profile of a polypeptide produced by a mammalian host cell, comprising introducing into said host cell an expression vector which comprises an isolated nucleic acid comprising a sequence encoding a fusion polypeptide, wherein said fusion polypeptide has β(1,4)-N-acetylglucosaminyltransferase III activity and comprises the Golgi localization domain of mannosidase II, and wherein said modified polypeptide has increased Fc-receptor binding or effector function as a result of said modification.
3. A method according to claim 1 or 2 , wherein said polypeptide is IgG or a fragment thereof.
4. A method according to claim 3 , wherein said polypeptide is IgG1 or a fragment thereof.
5. A method according to claim 3 , wherein said polypeptide is a fusion protein that includes a region equivalent to the Fc region of a human IgG.
6. A method for producing a polypeptide in a mammalian host cell, comprising:
a. culturing a mammalian host cell engineered to express at least one nucleic acid encoding a fusion polypeptide having β(1,4)-N-acetylglucosaminyltransferase III activity under conditions which permit the production of a polypeptide selected from the group consisting of a whole antibody molecule, an antibody fragment, and a fusion protein that includes a region equivalent to the Fc region of an immunoglobulin, wherein said fusion polypeptide is expressed in an amount sufficient to modify the oligosaccharides in the Fc region and increase the Fc-receptor binding or effector function of said polypeptide produced by said host cell and wherein said fusion polypeptide having β(1,4)-N-acetylglucosaminyltransferase III activity comprises the Golgi localization domain of mannosidase II; and
b. isolating said polypeptide.
7. A method according to claim 6 wherein said fusion polypeptide consists essentially of the catalytic domain of β(1,4)-N-acetylglucosaminyltransferase III and the Golgi localization domain of mannosidase II.
8. A method according to claim 6 , wherein said produced polypeptide selected from the group consisting of a whole antibody molecule, an antibody fragment, and a fusion protein that includes a region equivalent to the Fc region of an immunoglobulin exhibits at least 15% greater antibody-dependent cellular cytotoxicity compared to polypeptides produced in a host cell expressing wild-type β(1,4)-N-acetylglucosaminyltransferase III.
9. A method according to claim 6 , wherein said increased effector function is increased Fc-mediated cellular cytotoxicity.
10. A method according to claim 6 , wherein said polypeptide produced by said host cell exhibits increased Fc receptor binding affinity as a result of said modification.
11. A method according to claim 10 , wherein said Fc receptor is Fc activating receptor.
12. A method according to claim 10 , wherein said Fc receptor is FcγRIIIA receptor.
13. A method according to claim 6 , wherein said polypeptide produced by said host cell has an increased proportion of bisected oligosaccharides in the Fc region of said polypeptide.
14. A method according to claim 6 , wherein said polypeptide produced by said host cell has an increased proportion of nonfucosylated oligosaccharides in the Fc region of said polypeptide.
15. A method according to claim 14 , wherein said nonfucosylated oligosaccharides are hybrid.
16. A method according to claim 14 , wherein said nonfucosylated oligosaccharides are complex.
17. A method according to claim 6 , wherein said polypeptide produced by said host cell has an increased proportion of bisected, nonfucosylated oligosaccharides in the Fc region of said polypeptide.
18. A method according to claim 17 , wherein said bisected, nonfucosylated oligosaccharides are hybrid.
19. A method according to claim 17 , wherein said bisected, nonfucosylated oligosaccharides are complex.
20. A method according to claim 17 , wherein at least 20% of the oligosaccharides in the Fc region of said polypeptide are bisected, nonfucosylated.
21. A method according to claim 17 , wherein at least 25% of the oligosaccharides in the Fc region of said polypeptide are bisected, nonfucosylated.
22. A method according to claim 17 , wherein at least 30% of the oligosaccharides in the Fc region of said polypeptide are bisected, nonfucosylated.
23. A method according to claim 17 , wherein at least 35% of the oligosaccharides in the Fc region of said polypeptide are bisected, nonfucosylated.
24. A method for producing a polypeptide in a mammalian host cell, comprising:
a. culturing a mammalian host cell engineered to express at least one nucleic acid encoding a fusion polypeptide having GnT III activity and at least one nucleic acid encoding a polypeptide having Man II activity under conditions which permit the production of a polypeptide selected from the group consisting of a whole antibody molecule, an antibody fragment, and a fusion protein that includes a region equivalent to the Fc region of an immunoglobulin, wherein said fusion polypeptide is expressed in an amount sufficient to modify the oligosaccharides in the Fc region and increase the Fc-receptor binding or effector function of said polypeptide produced by said host cell and wherein said fusion polypeptide having GnT III activity comprises the Golgi localization domain of mannosidase II; and
b. isolating said polypeptide.
25. A method according to claim 24 wherein said fusion polypeptide consists essentially of the catalytic domain of GnT III and the Golgi localization domain of mannosidase II.
26. A method according to claim 24 , wherein said produced polypeptide selected from the group consisting of a whole antibody molecule, an antibody fragment, and a fusion protein that includes a region equivalent to the Fc region of an immunoglobulin exhibits at least 15% greater antibody-dependent cellular cytotoxicity compared to polypeptides produced in a host cell expressing wild-type β(1,4)-N-acetylglucosaminyltransferase III.
27. A method according to claim 24 , wherein said polypeptide produced by said host cell has an increased proportion of bisected, nonfucosylated oligosaccharides in the Fc region of said polypeptide.
28. A method according to claim 27 , wherein said bisected, nonfucosylated oligosaccharides are hybrid.
29. A method according to claim 27 , wherein said bisected, nonfucosylated oligosaccharides are complex.
30. A method according to claim 27 , wherein at least 20% of the oligosaccharides in the Fc region of said polypeptide are bisected, nonfucosylated.
31. A method according to claim 27 , wherein at least 25% of the oligosaccharides in the Fc region of said polypeptide are bisected, nonfucosylated.
32. A method according to claim 27 , wherein at least 30% of the oligosaccharides in the Fc region of said polypeptide are bisected, nonfucosylated.
33. A method according to claim 27 , wherein at least 35% of the oligosaccharides in the Fc region of said polypeptide are bisected, nonfucosylated.