Soluble intein fusion proteins and methods for purifying biomolecules
The present invention relates to fusion proteins comprising an N-intein polypeptide and an N-intein solubilization partner, and affinity chromatography matrices comprising such fusion proteins, as well as methods of using same.
1. A soluble fusion protein comprising an N-intein polypeptide capable of forming an active intein complex by associating with a second fusion protein comprising a C-intein polypeptide, and at least one cysteine of the N-intein is substituted with an amino acid selected from the group consisting of: threonine, lysine, asparagine, serine, methionine, and tyrosine, wherein the N-intein polypeptide is covalently attached to a solid support.
2. The N-intein polypeptide of claim 1 , wherein the solid support is a bead, a hollow fiber, a solid fiber, a pad, a gel, a membrane, a cassette, a column, a chip, a slide, a plate or a monolith.
3. The N-intein polypeptide of claim 1 , wherein the solid support is a chromatography resin.
4. A matrix comprising an N-intein polypeptide having at least one cysteine of the N-intein substituted with an amino acid selected from the group consisting of: threonine, lysine, asparagine, serine, methionine, and tyrosine, and attached, by covalent attachment, to a solid support.
5. The matrix of claim 4 , wherein the solid support is a chromatography resin.
6. The matrix of claim 5 , wherein the chromatography resin includes a hydrophilic polyvinyl ether base.
7. The matrix of claim 4 , wherein the solid support is a bead, a hollow fiber, a solid fiber, a pad, a gel, a membrane, a cassette, a column, a chip, a slide, a plate or a monolith.
8. The matrix of claim 7 , wherein the solid support is a magnetic bead.
9. The matrix of claim 8 , wherein the solid support comprises controlled pore glass, silica, zirconium oxide, titanium oxide, agarose, polymethacrylate, polyacrylate, polyacrylamide, polyvinyl alcohol, polystyrene or derivatives thereof.