Process for producing sugar chains using β1,3-N-acetylglucosaminyltransferase
The present invention provides a novel polypeptide having a β1,3-N-acetylglucosaminyltransferase activity, an agent for synthesizing a sugar chain comprising the polypeptide, a process for producing a sugar chain or a complex carbohydrate using the agent for synthesizing a sugar chain, DNA encoding the polypeptide, a process for producing the polypeptide, an antibody against the polypeptide, and a diagnosis method and a medicament for treatment for inflammation, cancer or tumor metastasis using the DNA or the antibody. The present invention is useful for synthesis of a useful sugar chain and diagnosis and treatment for inflammatory diseases, cancer or tumor metastasis.
1. A process for producing a sugar chain or complex carbohydrate comprising the steps of:
a) selecting an enzyme source selected from the group consisting of (i) a polypeptide comprising SEQ ID NO: 1, (ii) a polypeptide comprising positions 39 to 378 of SEQ ID NO: 1, and (iii) a polypeptide comprising an amino acid sequence having 95% or more of homology with the amino acid sequence in the polypeptide according to (i) or (ii), and has β1,3-N-acetylglucosaminyltransferase activity,
b) an acceptor selected from i) lactosylceramide (Galβ1-4Glc-ceramide) or paragloboside (Galβ1-4GlcNAcβ1-3Galβ1-4Glc-ceramide), ii) galactose, N-acetyllactosamine (Galβ1-4GlcNAc), Galβ1-3GlcNAc or lactose (Galβ1-4Glc), iii) an oligosaccharide having galactose, N-acetyllactosamine (Galβ1-4GlcNAc), Galβ1-3GlcNAc or lactose structure in its non-reducing terminal, and iv) a complex carbohydrate having galactose, N-acetyllactosamine, Galβ1-3GlcNAc or lactose structure in its non-reducing terminal, and
c) N-acetylglucosamine uridine 5′-diphosphate (UDP-GlcNAc)
to be present in an aqueous medium to produce and accumulate a sugar chain or complex carbohydrate in which N-acetylglucosamine is added via β1,3-linkage to a galactose residue of the acceptor in the aqueous medium, and recovering the sugar chain or complex carbohydrate from the aqueous medium.
2. A process for producing a galactose-added sugar chain or complex carbohydrate by using the N-acetylglucosamine-added sugar chain or complex carbohydrate obtained by the process according to claim 1 as an acceptor, which comprises allowing
a) the acceptor,
b) GlcNAc β1,4-galactosyltransferase, and
c) uridine 5′-diphosphate galactose (UDP-Gal)
to be present in an aqueous medium to produce and accumulate a reaction product in which galactose is added via β3 1,4-linkage to an N-acetylglucosamine residue at the non-reducing terminal of the acceptor in the aqueous medium, and recovering the galactose-added sugar chain or complex carbohydrate from the aqueous medium.
3. A process for producing a poly-N-acetyllactosamine sugar chain-added sugar chain or complex carbohydrate comprising the steps of:
a) selecting an enzyme source selected from the group consisting of (i) a polypeptide comprising SEQ ID NO: 1, (ii) a polypeptide comprising positions 39 to 378 of SEQ ID NO: 1, and (iii) a polypeptide comprising an amino acid sequence having 95% or more of homology with the amino acid sequence in the polypeptide according to (i) or (ii), and has β1,3-N-acetylglucosaminyltransferase activity,
b) GlcNAc β1,4-galactosyltransferase,
c) an acceptor selected from i) lactosylceramide (Galβ1-4Glc-ceramide) or paragloboside (Galβ1-4GlcNAcβ1-3Galβ1-4Glc-ceramide), ii) galactose, N-acetyllactosamine (Galβ1-4GlcNAc), Galβ1-3GlcNAc or lactose (Galβ1-4Glc), iii) an oligosaccharide having galactose, N-acetyllactosamine (Galβ1-4GlcNAc), Galβ1-3GlcNAc or lactose (Gal β1-4Glc) structure in its non-reducing terminal, iv) a complex carbohydrate having galactose, N-acetyllactosamine, Galβ1-3GlcNAc or lactose structure in its non-reducing terminal and v) a sugar chain or complex carbohydrate obtained by the process according to claim 1 or 2 ,
d) uridine 5′-diphosphate N-acetylglucosamine (UDP-GlcNAc), and
e) uridine 5′-diphosphate galactose (UDP-Gal)
to be present in an aqueous medium to produce and accumulate a reaction product in which poly-N-acetyllactosamine sugar chain is added to the non-reducing terminal of the acceptor in the aqueous medium, and recovering the poly-N-acetyllactosamine sugar chain-added sugar chain or complex carbohydrate from the aqueous medium.
4. The process according to any one of claims 1 - 3 , wherein the β1,3-N-acetylglucosaminyltransferase activity is an activity to transfer N-acetylglucosamine via β1,3-linkage to a galactose residue present in its non-reducing terminal of a sugar chain.
5. The process according to claim 4 , wherein the β1,3-N-acetylglucosaminyltransferase activity is an activity to transfer N-acetylglucosamine via β1,3-linkage to a galactose residue present in its non-reducing terminal of a sugar chain of an acceptor selected from i) galactose, N-acetyllactosamine (Galβ1-4GlcNAc), Galβ1-3GlcNAc or lactose (Galβ1-4Glc), ii) an oligosaccharide having galactose, N-acetyllactosamine, Galβ1-3GlcNAc or lactose structure in its non-reducing terminal, and iii) a complex carbohydrate having galactose, N-acetyllactosamine, Galβ1-3GlcNAc or lactose structure in its non-reducing terminal.
6. The process according to claim 5 , wherein the complex carbohydrate having galactose, N-acetyllactosamine, Galβ1-3GlcNAc or lactose structure in its non-reducing terminal is lactosylceramide (Galβ1-4Glc-ceramide) or paragloboside (Galβ1-4GlcNAcβ1-3Galβ1-4Glc-ceramide).
7. The process according to claim 5 or 6 , wherein the complex carbohydrate is a complex carbohydrate selected from a glycoprotein, a glycolipid, a proteoglycan, a glycopeptide, a lipopolysaccharide, a peptidoglycan and a glycoside in which a sugar chain is linked to a steroid compound.
8. A process for producing a sugar chain or complex carbohydrate, which comprises the steps of using a transformant harboring a recombinant vector comprising DNA or RNA encoding (i) a polypeptide comprising SEQ ID NO:1, (ii) a polypeptide comprising positions 39 to 378 of SEQ ID NO:1, and (iii) a polypeptide comprising an amino acid sequence having 95% or more of homology with the amino acid sequence in the polypeptide according to (i) or (ii), and has β1,3-N-acetylglucosaminyltransferase activity to produce and accumulate a sugar chain comprising a saccharide selected from the group consisting of GlcNAcβ1-3Galβ1-4Glc-ceramide, a lacto-series glycolipid (a glycolipid having Galβ1-3GlcNAcβ1-3Galβ1-4Glc-ceramide as a backbone), a neolacto-series glycolipid (a glycolipid having Galβ1-4GlcNAcβ1-3Galβ1-4Glc-ceramide as a backbone), a saccharide having GlcNAcβ1-3Gal structure, a saccharide having GlcNAcβ1-3Galβ1-4GlcNAc structure, a saccharide having GlcNAcβ1-3Galβ1-3GlcNAc structure, a saccharide having GlcNAcβ1-3Galβ1-4Glc structure, a saccharide having (Galβ1-4GlcNAcβ1-3) n Galβ1-4G1cNAc structure wherein n is 1 or more and a saccharide having a (Galβ1-4GlcNAcβ1-3) n Galβ1-4Glc structure wherein n is 1 or more, or a complex carbohydrate containing the sugar chain, and recovering the sugar chain or complex carbohydrate from the culture.
9. The process according to claim 8 , wherein the recombinant vector comprises SEQ ID NO:2.
10. The process according to claim 8 , wherein the recombinant vector comprises positions 135 to 1268 of SEQ ID NO:2.
11. The process according to claim 8 , wherein the recombinant vector comprises positions 249 to 1268 of SEQ ID NO:2.
12. The process according to claim 8 , wherein the recombinant vector comprises a nucleotide sequence that hybridizes to the nucleotide sequence (i) encoding SEQ ID NO: 1, (ii) SEQ ID NO:2, (iii) positions 135 to 1268 of SEQ ID NO:2 or (iv) positions 249 to 1268 of SEQ ID NO:2 at 65° C., in the presence of 0.7 to 1.0M sodium chloride followed by washing at 65° C. with 0.1×SSC, and encodes a polypeptide having β1,3-N-acetylglucosaminyltransferase activity.
13. The process according to claim 12 , wherein the β1,3-N-acetylglucosaminyltransferase activity is an activity to transfer N-acetylglucosamine via β1,3-linkage to a galactose residue present in its non-reducing terminal of a sugar chain.
14. The process according to claim 12 or 13 , wherein the β1,3-N-acetylglucosaminyltransferase activity is an activity to transfer N-acetylglucosamine via β1,3-linkage to a galactose residue present in its non-reducing terminal of a sugar chain of an acceptor selected from i) galactose, N-acetyllactosamine (Galβ1-4GlcNAc), Galβ1-3GlcNAc or lactose (Galβ1-4Glc), ii) an oligosaccharide having galactose, N-acetyllactosamine, Galβ1-3GlcNAc or lactose structure in its non-reducing terminal, and iii) a complex carbohydrate having galactose, N-acetyllactosamine, Galβ1-3GlcNAc or lactose structure in its non-reducing terminal.
15. The process according to claim 14 , wherein the complex carbohydrate having galactose, N-acetyllactosamine, Galβ1-3GlcNAc or lactose structure in its non-reducing terminal is lactosylceramide or paragloboside.
16. The process according to claim 14 or 15 , wherein the complex carbohydrate is a complex carbohydrate selected from a glycoprotein, a glycolipid, a proteoglycan, a glycopeptide, a lipopolysaccharide, a peptidoglycan and a glycoside in which a sugar chain is linked to a steroid compound.
17. The process according to claim 8 , wherein the transformant is selected from the group consisting of a microorganism, an animal cell, a plant cell and an insect cell.
18. The process according to claim 17 , wherein the transformant is a microorganism belonging to the genus Eseherichia.
19. The process according to claim 17 , wherein the transformant is an animal cell selected from the group consisting of a mouse myeloma cell, a rat myeloma cell, a mouse hybridoma cell, a CHO cell, a BHK cell, an African green monkey kidney cell, a Namalwa cell, a Namalwa KJM-1 cell, a human fetal kidney cell and a human leukemia cell.
20. The process according to claim 17 , wherein the transformant is a plant cell selected from the group consisting of plant cells of tobacco, potato, tomato, carrot, soybean, rape, alfalfa, rice plant, wheat, barley, rye, corn or flax.
21. The process according to claim 17 , wherein the transformant is an insect cell selected from the group consisting of Spodoptera frugiperda ovarian cells, Trichoplusia ni ovarian cells and silkworm ovarian cells.
22. The process according to claim 8 , wherein the transformant is a transgenic plant.
23. A process for producing a sugar chain or complex carbohydrate, which comprises using the transgenic plant according to claim 22 , further comprising recovering the sugar chain or complex carbohydrate.
24. The process according to any one of claims 1 to 23 , wherein the complex carbohydrate is selected from a glycoprotein, a glycolipid, a proteoglycan, a glycopeptide, a lipopolysaccharide, a peptidoglycan and a glycoside in which a sugar chain is linked to a steroid compound.