Copper supplementation for control of glycosylation in mammalian cell culture process
The present invention pertains to a cell culture medium comprising copper as a media supplement, which was shown to control recombinant protein glycosylation and methods of using thereof. The present invention further pertains to a method of controlling or manipulating glycosylation of a recombinant protein of interest in a large scale cell culture.
1. A method for achieving a predetermined galactosylation profile of an anti-α4-integrin antibody comprising:
culturing host cells producing the anti-α4-integrin antibody in a cell culture comprising an amount of copper within a target copper concentration range, wherein the target copper concentration range in the cell culture is between 200 nM and 500 nM, wherein the target copper concentration is achieved by supplementing the cell culture with a yeast hydrolysate comprising copper.
2. The method of claim 1 , comprising supplementing the cell culture with the yeast hydrolysate comprising copper if the copper concentration in the cell culture is below the target copper concentration range.
3. The method of claim 1 , wherein the target copper concentration is maintained through a feedback loop.
4. The method of claim 1 , wherein the copper concentration is constantly monitored and maintained within the target copper concentration range.
5. The method of claim 1 , wherein the target copper concentration is achieved with a single dose of the yeast hydrolysate comprising copper.
6. The method of claim 1 , wherein the anti-α4-integrin antibody is produced by a eukaryotic host cell.
7. The method of claim 6 , wherein the eukaryotic host cell is a mammalian host cell.
8. The method of claim 1 , wherein the copper concentration alters the levels of the isoform variants of the anti-α4-integrin antibody.
9. The method of claim 1 , wherein the anti-α4-integrin antibody is natalizumab.
10. The method of claim 1 , wherein the yeast hydrolysate used to supplement the cell culture comprises copper (II) sulfate.
11. The method of claim 1 , wherein the target copper concentration range in the cell culture is transitioned to between 200 nM and 500 nM after an initial culture comprising a target copper concentration of between 20 nM and 50 nM.