Apparatus and method for mixed-bed lectin chromatography

• US 20050245737A1
• Filed: 04/21/2005
• Published: 11/03/2005
• Est. Priority Date: 04/22/2004
• Status: Abandoned Application

• Current Assignee: The Board of Regents of the University of Colorado (University of Colorado System)
• Original Assignee: The Board of Regents of the University of Colorado (University of Colorado System)
• Inventors: Cummings, Richard D.
• Application Number:
  US11/111,322
• Publication Number:
  US 20050245737A1
• Time in Patent Office: Days
• US Class Current: 536/55.300
• CPC Class Codes: C07H 5/04 to nitrogen
• CPC Class Codes: C07H 5/06 Aminosugars

Abstract

The present invention contemplates an apparatus and method for isolating glycoconjugates from mixtures or contaminated mixtures thereof. In the present invention, a bed or other support element comprising a mixture of immobilized lectins is provided. The mixture of glycoconjugates is passed over the mixed lectin bed wherein glycoconjugates which correspond to the lectins in the bed are bound thereto while non-glycoconjugates flow away. Thus, the method can be used to isolate glycoproteins from mixtures of glycoproteins and non-glycosylated proteins, glycopeptides from mixtures of glycopeptides and non-glycosylated peptides, glycolipids from non-glycosylated lipids, and free oligosaccharides from extracts or preparations. This invention solves the problem of isolating glycoconjugates from complex mixtures of glycoconjugates with non-gyconconjugates. For example, in most cells, a large fraction of the total macromolecules are not glycosylated. Glycomics and glycoproteomics specifically are concerned with macromolecules which contain carbohydrates. Thus, the mixed bed lectin chromatography described herein will expand both glycomics and glycoproteomics, which are currently hampered by lack of methods or devices or approaches able to be used to generally isolate all or most of the glycoconjugates in cells or extracts of cells in a simple and direct approach that has few steps.

Claims

1. A method of separating glycosylated molecules from non-glycosylated molecules, comprising:

providing a support element having at least two types of lectins immobilized on a support material;

providing a mixture of molecules comprising glycosylated molecules and non-glycosylated molecules;

combining the mixture of molecules with the support element having the at least two types of immobilized lectins;

removing the glycosylated molecules which are bound to the at least two types of immobilized lectins on the support element by washing the support element with a mixed hapten buffer comprising one or more saccharides which bind to the at least two types of immobilized lectins on the support element thereby displacing the glycosylated molecules from the at least two types of immobilized lectins; and

collecting the glycosylated molecules which are eluted from the support element due to displacement from the at least two types of immobilized lectins by the mixed hapten buffer.

2. The method of claim 1 comprising the additional step of collecting the non-glycosylated molecules which pass over the support element without binding to the at least two types of immobilized lectins after combining the mixture of molecules with the support element.

3. The method of claim 1 wherein in the step of providing the support element, the at least two types of immobilized lectins comprise at least one of fucose, galactose, N-acetylglucosamine, N-acetylgalactosamine, mannose, glucose, sialic acids, and derivatives thereof.

4. The method of claim 1 wherein in the step of providing a support element, the at least two types of immobilized lectins are selected from the groups of lectins in Table I and Table II.

5. The method of claim 1 wherein in the step of providing a support element, the at least two types of immobilized lectins are selected form the lectins in Appendix I.

6. The method of claim 1 wherein in the step of providing the support element, the support element comprises a chromatography column.

7. The method of claim 1 wherein in the step of removing the glycosylated molecules, the mixed hapten buffer comprises at least one saccharide selected from the group consisting of fucose, mannose, α

-methyl-mannose, GlcNAc, GalNAc, galactose, lactose, raffinose, stachyose, glucose, sialic acids, chitobiose, chitotriose, chitotetraose, and maltose.

8. The method of claim 1 wherein in the step of providing a mixture of molecules comprising glycosylated molecules, the glycosylated molecules comprise glycoproteins, glycopeptides, glycolipids, glycosaminoglycans, free oligosaccharides, and/or polysaccharides, or other glycoconjugates.

9. A chromatography column comprising a support element comprising two or more different lectins immobilized thereon.

10. The chromatography column of claim 9 wherein the two or more lectins immobilized thereon are selected from the lectins listed in Appendix I, Table I, and Table II.

11. A method of separating glycosylated molecules from non-glycosylated molecules, comprising:

providing a support material having at least two types of lectins immobilized thereon;

providing a mixture of molecules comprising glycosylated molecules and non-glycosylated molecules;

combining the mixture of molecules with the support material having the at least two types of immobilized lectins; and

removing the glycosylated molecules which are bound to the at least two types of immobilized lectins on the support material by washing the support material with a mixed hapten buffer comprising one or more saccharides which bind to the at least two types of immobilized lectins on the support material thereby displacing the glycosylated molecules from the at least two types of immobilized lectins on the support material.

12. The method of claim 11 comprising the additional step of collecting the glycosylated molecules which are eluted from the support material due to displacement from the at least two types of immobilized lectins by the mixed hapten buffer.

13. The method of claim 11 comprising the additional step of collecting the non-glycosylated molecules which pass over the support material without binding to the at least two types of immobilized lectins after combining the mixture of molecules with the support material.

14. The method of claim 11 wherein in the step of providing the support material, the at least two types of immobilized lectins comprise at least one of fucose, galactose, N-acetylglucosamine, N-acetylgalactosamine, mannose, glucose, sialic acids, and derivatives thereof.

15. The method of claim 11 wherein in the step of providing a support material, the at least two types of immobilized lectins are selected from the groups of lectins in Table I and Table II.

17. The method of claim 11 wherein in the step of providing the support material, the support material comprises a portion of a chromatography column.

18. The method of claim 11 wherein in the step of removing the glycosylated molecules, the mixed hapten buffer comprises at least one saccharide selected from the group consisting of fucose, mannose, α

-methyl-mannose, GlcNAc, GalNAc, galactose, lactose, raffinose, stachyose, glucose, sialic acids, chitobiose, chitotriose, chitotetraose, and maltose.

19. The method of claim 11 wherein in the step of providing a mixture of molecules comprising glycosylated molecules, the glycosylated molecules comprise glycoproteins, glycopeptides, glycolipids, glycosaminoglycans, free oligosaccharides, and/or polysaccharides, or other glycoconjugates.

16. The method of clam 11 wherein in the step of providing a support material, the at least two types of immobilized lectins are selected form the lectins in Appendix I.

20. A chromatography apparatus comprising a support material comprising two or more different lectins immobilized thereon.

21. The chromatography apparatus of claim 20 wherein the two or more lectins immobilized thereon are selected from the lectins listed in Appendix I, Table I, and Table II.