Method for the recombinant production and purification of protein kinases
A method for the recombinant production and purification of a protein kinase selected from the group consisting of tyrosine protein kinases and serine/threonine kinases by expressing a nucleic acid encoding said kinase in a microbial host cell, forming inclusion bodies containing said kinase, isolating, solubilizing, naturing, and purifying said kinase wherein said purification is performed by hydrophobic interaction with an hydrophobic adsorbent under conditions whereby at least 70% of said protein kinase are not bound to said adsorbent and the protein kinase not bound to said adsorbent is recovered.
1. A method for the recombinant production and purification of a correctly folded protein kinase selected from the group consisting of tyrosine protein kinases and serine/threonine kinases comprising:
a) expressing a nucleic acid encoding said protein kinase in a microbial host cell, wherein inclusion bodies containing said protein kinase are formed in said host cell,
b) isolating said protein kinase from the cell, solubilizing said protein kinase, and then renaturing said protein kinase to provide a renatured protein kinase, and
c) purifying said renatured protein kinase by hydrophobic interaction chromatography with a hydrophobic adsorbent wherein said renatured protein kinase is applied directly to said hydrophobic adsorbent in an aqueous solution comprising at least a 1 M salt solution wherein the cation is selected from the group consisting of sodium, potassium and ammonium, and an anion selected from the group consisting of chloride, phosphate and sulfate, except that where the cation is ammonium, the anion is not sulfate,
whereby at least 70% of said protein kinase recovered is correctly folded and is not bound to said hydrophobic adsorbent.
2. The method according to claim 1 , wherein the hydrophobic adsorbent comprises a gel matrix substituted with hydrophobic ligands in the range of 10-50 μmol/ml gel, wherein the hydrophobic ligands are selected from the group C 2 -C 8 alkyl residues or simple aryl(phenyl) residues.
3. The method according to claim 2 , wherein the hydrophobic adsorbent comprises a cross-linked agarose substituted with phenyl-, butyl- or octyl groups.
4. The method according to claim 3 , wherein the hydrophobic adsorbent is selected from the group consisting of phenyl-, octyl- or butyl-sepharose.
5. The method of claim 1 , wherein the salt is KCl or NaCl.
6. The method according to claim 1 , wherein the aqueous solution comprises in addition at least 0.5 M arginine, guanidine or a compound having the general formula I
R 2 —CO—NRR 1 (I),
or combinations thereof,
wherein
R and R 1 are hydrogen or a saturated or unsaturated branched or unbranched C 1 -C 4 alkyl chain and
R 2 is hydrogen, NHR 1 or a saturated or unsaturated branched or unbranched C 1 -C 3 alkyl chain.
7. A method for the recombinant production and purification a correctly folded protein kinase selected from the group consisting of a Src, a PKB, a c-Met, a Lck, an Aurora or a p38 MAPK protein kinase comprising:
a) expressing a nucleic acid encoding said protein kinase in a microbial host cell, wherein inclusion bodies containing said protein kinase are formed in said host cell,
b) isolating said protein kinase from the cell, solubilizing said protein kinase, and then renaturing said protein kinase to provide a renatured protein kinase, and
c) purifying said renatured protein kinase by hydrophobic interaction chromatography with a hydrophobic adsorbent wherein said renatured protein kinase is applied directly to said hydrophobic adsorbent in an aqueous solution comprising at least a 1 M salt solution wherein the cation is selected from the group consisting of sodium, potassium and ammonium, and an anion selected from the group consisting of chloride, phosphate and sulfate, except that where the cation is ammonium, the anion is not sulfate,
whereby at least 70% of said protein kinase recovered is correctly folded and is not bound to said hydrophobic adsorbent.
8. The method according to claim 7 , wherein the hydrophobic adsorbent comprises a gel matrix substituted with hydrophobic ligands in the range of 10-50 μmol/ml gel, wherein the hydrophobic ligands are selected from the group comprising C 2 -C 8 alkyl residues or simple aryl(phenyl) residues.
9. The method according to claim 8 , wherein the hydrophobic adsorbent comprises a cross-linked agarose substituted with phenyl-, butyl- or octyl groups.
10. The method according to claim 9 , wherein the hydrophobic adsorbent is selected from the group consisting of phenyl-, octyl- or butyl-sepharose.
11. The method of claim 7 , wherein the salt is KCl or NaCl.
12. The method according to claim 7 , wherein the aqueous solution comprises in addition at least 0.5 M arginine, guanidine or a compound having the general formula I
R 2 —CO—NRR 1 (I),
or combinations thereof,
wherein
R and R 1 are hydrogen or a saturated or unsaturated branched or unbranched C 1 -C 4 alkyl chain and
R 2 is hydrogen, NHR 1 or a saturated or unsaturated branched or unbranched C 1 -C 3 alkyl chain.