Method of producing recombinant proteins with mannose-terminated N-glycans
View Patent ↗We describe a method of expressing a recombinant protein comprising mannose-terminated N-glycans from a host cell, the method comprising: (a) introducing a nucleic acid encoding a recombinant protein into a Chinese Hamster Ovary (CHO) cell comprising a mutation in the GnT 1 gene (GenBank Accession Number AF343963) leading to loss of GnT 1 function; and (c) expressing the recombinant protein from the host cell, in which the expressed recombinant protein comprises a mannose-terminated glycan structure, and in which the method does not include a step of introducing functional GnT-1 into the host cell. The method may be used for producing recombinant glucocerebrosidase with a mannose-terminated glycan structure, suitable for treatment or prevention of Gaucher's Disease.
1. A method of expressing a recombinant protein comprising mannose-terminated N-glycans from a host cell, the method comprising:
(a) introducing a nucleic acid encoding a recombinant protein into a host cell comprising a mutation in the GnT I gene leading to loss of GnT I function, the host cell is a Chinese Hamster Ovary (CHO) cell selected with Ricinus communis agglutinin I (RCA-I) or a descendent thereof; and
(b) expressing the recombinant protein from the host cell, in which the expressed recombinant protein comprises mannose-terminated N-glycans structure
in which the method does not include a step of introducing functional GnT I into the host cell.
2. A method of expressing a recombinant protein comprising mannose-terminated N-glycans from a host cell, the method comprising:
(a) introducing a nucleic acid encoding a recombinant protein into a host cell comprising a mutation in the GnT I gene leading to loss of GnT I function, wherein the host cell is a Chinese Hamster Ovary (CHO) cell selected with Ricinus communis agglutinin I (RCA-I) or a descendent thereof; and
(b) expressing the recombinant protein from the host cell, in which the expressed recombinant protein comprises mannose-terminated N-glycans structure;
wherein the method does not include a step of introducing functional GnT I into the host cell and the CHO cell was selected with RCA-I by culturing CHO cells in the presence of Ricinus communis agglutinin I (RCA-I) and selecting cells which survive the culture.
3. The method according to claim 1 , in which the host cell is adapted to suspension culture.
4. The method according to claim 1 , in which the host cell comprises a JW152 cell (deposited at ATCC under the Budapest Treaty as accession number PTA-9657).
5. The method according to claim 1 , in which at step (b) an expression construct comprising nucleic acid encoding the recombinant protein in an expression vector is introduced into the host cell.
6. The method according to claim 1 , in which the nucleic acid encoding the recombinant protein is transformed or stably integrated into the host cell.
7. The method according to claim 1 , further comprising the step of isolating and/or purifying the expressed recombinant protein.
8. The method according to claim 1 , in which the recombinant protein comprises:
(a) a sequence of SEQ ID NO. 3 or a variant, homologue, derivative or fragment thereof having glucocerebrosidase activity;
(b) a tumour-specific or tumour-associated antigen; or
(c) a viral antigen.
9. The method according to claim 1 , in which the nucleic acid comprises a sequence of SEQ ID NO. 4 or a variant, homologue, derivative or fragment thereof encoding a protein comprising glucocerebrosidase activity.
10. A JW152 cell (deposited at ATCC under the Budapest Treaty as accession number PTA-9657) comprising a nucleic acid sequence encoding a recombinant protein.
11. A method of expressing a recombinant protein comprising mannose-terminated N-glycans from a JW152 host cell, the method comprising:
(a) providing a JW152 host cell (deposited at ATCC under the Budapest Treaty as accession number PTA-9657) comprising a nucleic acid encoding a protein having glucocerebrosidase activity, MUC1, HER2/neu or carcinoembryonic antigen (CEA); and
(b) allowing the recombinant protein to be expressed from the JW152 host cell in which the method does not include a step of introducing functional GnT I into the host cell.
12. The method according to claim 2 , in which the CHO cells were cultured in the presence of RCA-I at a concentration of between 0.1 μg/ml to 100 μg/ml.
13. The method according to claim 2 , in which the CHO cells were cultured in the presence of RCA-I at a concentration of between 0.1 μg/ml to 50 μg/ml.
14. The method according to claim 2 , in which the CHO cells were cultured in the presence of RCA-I at a concentration of between 0.1 μg/ml to 20 μg/ml.
15. The method according to claim 2 , in which the CHO cells are exposed to RCA-I for a period of at least an hour.
16. The method according to claim 2 , in which the CHO cells are exposed to RCA-I for a period of 2 to 12 hours.
17. The method according to claim 2 , in which the CHO cells are exposed to RCA-I for a period of 2 to 3 days.
18. The method according to claim 2 , further comprising a step of selecting CHO cells which do not react with RCA-I in an agglutination test.
19. The method according to claim 5 , in which the expression vector is pcDNA3.1.
20. The method according to claim 11 , in which the recombinant protein comprising mannose-terminated N-glycans is a protein having glucocerebrosidase activity, MUC1, HER2/neu, or carcinoembryonic antigen (CEA).
21. The JW152 cell according to claim 10 , in which the nucleic acid sequence encodes a protein with glucocerebrosidase activity, MUC1, HER2/neu, or carcinoembryonic antigen (CEA).
22. The JW152 cell according to claim 10 , in which the nucleic acid sequence is capable of expression of the recombinant protein.
23. The method according to claim 8 , wherein the tumour-specific or tumour-associated antigen is selected from the group consisting of MUC1, HER2/neu, carcinoembryonic antigen (CEA) and antigenic portions thereof.