Expression of modified glycoproteins and glycopeptides

US10457970B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10457970-B2
Application numberUS-201715799785-A
CountryUS
Kind codeB2
Filing dateOct 31, 2017
Priority dateNov 1, 2016
Publication dateOct 29, 2019
Grant dateOct 29, 2019

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

The present invention provides recombinant cells that contain a modification causing altered expression or function of at least one mannosyl transferase enzyme. As a result of the modification the cells produce a glycoprotein or glycopeptide that has an N-linked glycan profile that is simplified or humanized. The glycoprotein or glycopeptide can have at least 25% fewer high mannose structures on than the glycoprotein or glycopeptide produced by a cell that does not have the modification. In some embodiments the modification is a deletion, knock out, or disruption of a gene encoding a mannosyl transferase, which can be in an Alg3 gene. Therefore, the proteins produced avoid many of the problems associated with the therapeutic use of glycoproteins from species having foreign or plant-like patterns of glycosylation. The invention also provides compositions of the glycoproteins or glycopeptides and methods of making them.

First claim

Opening claim text (preview).

The invention claimed is: 1. A recombinant cell of the Class Labyrinthulomycetes comprising a genetic modification of a gene that encodes a mannosyl transferase, and further comprising a recombinant nucleic acid encoding a functional glycoprotein or glycopeptide, wherein the cell produces a heterologous glycoprotein or glycopeptide having an N-linked glycan profile that has at least 25% fewer high mannose structures than the N-linked glycan profile from a reference cell that does not comprise the genetic modification in the gene that encodes the mannosyl transferase. 2. The cell of claim 1 wherein the genetic modification is selected from a deletion, an insertion, a replacement, or a disruption. 3. The cell of claim 1 wherein the genetic modification is a deletion, and the mannosyl transferase is an alpha-1,3-mannosyl transferase. 4. The cell of claim 3 wherein the mannosyl transferase is of the class EC 2.4.1.258. 5. The cell of claim 1 wherein the glycoprotein is an antibody. 6. The cell of claim 5 wherein the heterologous glycoprotein is selected from the group consisting of: trastuzumab, eculizumab, natalizumab, cetuximab, omalizumab, usteinumab, panitumumab, and adalimumab, or a functional fragment of any of them. 7. The cell of claim 3 wherein the heterologous glycoprotein or glycopeptide has an N-linked glycan profile having at least 50% fewer high mannose N-linked glycans than the N-linked glycan profile from a Labyrinthulomycetes cell that does not comprise the mannosyl transferase deletion. 8. The cell of claim 1 wherein the glycoprotein or glycopeptide has an N-linked glycan profile having less than 50% high mannose structures. 9. The Labyrinthulomycetes cell of claim 3 selected from the group consisting of: Aurantiochytrium, Schizochytrium , and Thraustochytrium , further wherein the genetic modification is a deletion, and the mannosyl transferase is alg3. 10. The cell of claim 9 which is an Aurantiochytrium sp. 11. The cell of claim 1 wherein the glycoprotein or glycopeptide comprises at least 50% fewer high mannose structures. 12. The cell of claim 1 wherein the glycoprotein or glycopeptide comprises at least 25% more paucimannose structures versus the cell that does not comprise the mannosyl transferase genetic modification. 13. The cell of claim 1 wherein more than 50% of the N-linked glycans comprise a paucimannose structure. 14. The cell of claim 13 wherein the paucimannose structure comprises a Man3 structure. 15. A method of producing a glycoprotein or glycopeptide that comprises a simplified N-glycan profile comprising: a) performing a genetic modification in a gene that encodes a mannosyl transferase in a host cell of the Class Labyrinthulomycetes; b) cultivating the host cell; c) harvesting a glycoprotein or glycopeptide from the cell that has a simplified N-linked glycan profile wherein at least 50% of the N-linked glycans comprise a Man3 and/or Man4 glycan structure. 16. The method of claim 15 wherein the mannosyl transferase is an alpha-1,3-mannosyl transferase. 17. The method of claim 16 wherein the mannosyl transferase is of the class EC 2.4.1.258. 18. The method of claim 16 wherein the genetic modification is a deletion, and the glycoprotein is an antibody. 19. The cell of claim 18 wherein the glycoprotein antibody is selected from the group consisting of: trastuzumab, eculizumab, natalizumab, cetuximab, omalizumab, usteinumab, panitumumab, and adalimumab, or a functional fragment of any of them. 20. The method of claim 15 wherein the glycoprotein or glycopeptide comprises at least 50% fewer N-linked glycans versus a host cell that does not comprise the mannosyl transferase deletion. 21. The method of claim 15 wherein the N-linked glycan profile comprises less than 50% high mannose structures. 22. The method of claim 15 wherein the Labyrinthulomycete cell is selected from the group consisting of: Aurantiochytrium, Schizochytrium , and Thraustochytrium , further wherein the genetic modification is a deletion and the mannosyl transferase is alg3. 23. The method of claim 22 wherein the Labyrinthulomycete is an Aurantiochytrium. 24. The method of claim 15 wherein the glycoprotein or glycopeptide comprises at least 50% fewer high mannose structures. 25. The method of claim 15 wherein the glycoprotein or glycopeptide comprises at least 25% more paucimannose structures versus the cell that does not comprise the mannosyl transferase deletion. 26. The method of claim 15 wherein more than 50% of the N-linked glycans comprise a man3 glycan structure. 27. The method of claim 15 wherein the N-glycan structure comprises at least 70% Man3 and/or Man4 structures. 28. The recombinant cell of claim 3 wherein the gene that encodes a mannosyl transferase is alg3. 29. The method of claim 15 wherein the genetic modification is a deletion, and the gene that encodes a mannosyl transferase is alg3.

Assignees

Inventors

Classifications

  • against translation products of oncogenes · CPC title

  • Hexosyltransferases (2.4.1) · CPC title

  • C12P21/005Primary

    Glycopeptides, glycoproteins · CPC title

  • Dolichyl-P-Man:Man5GlcNAc2-PP-dolichol alpha-1,3-mannosyltransferase (2.4.1.258) · CPC title

  • Specific host cells or culture conditions, e.g. components, pH or temperature · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US10457970B2 cover?
The present invention provides recombinant cells that contain a modification causing altered expression or function of at least one mannosyl transferase enzyme. As a result of the modification the cells produce a glycoprotein or glycopeptide that has an N-linked glycan profile that is simplified or humanized. The glycoprotein or glycopeptide can have at least 25% fewer high mannose structures o…
Who is the assignee on this patent?
Conagen Inc
What technology area does this patent fall under?
Primary CPC classification C12P21/005. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Oct 29 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).