Method for preparing recombinant granulocyte colony stimulating factor cysteine muteins
The present invention relates to novel methods for making and refolding insoluble or aggregated proteins having free cysteines in which a host cell expressing the protein is exposed to a cysteine blocking agent. The soluble, refolded proteins produced by the novel methods can then be modified to increase their effectiveness. Such modifications include attaching a PEG moiety to form PEGylated proteins.
1. A method for preparing a biologically active recombinant granulocyte colony-stimulating factor (G-CSF) protein lacking a non-natural N-terminal methionine residue, the method comprising the steps of:
(a) obtaining an Escherichia coli ( E. coli ) host cell transformed with a DNA encoding a G-CSF protein fused to the C-terminus of the E. coli STII signal sequence;
(b) growing the E. coli host cell under conditions that cause the host cell to express the G-CSF protein and secrete the G-CSF protein into the E. coli periplasm, wherein the STII signal sequence is cleaved enzymatically from the G-CSF protein in the periplasm;
(c) lysing the cells;
(d) separating the soluble proteins from the insoluble proteins, wherein the insoluble proteins comprise the G-CSF;
(e) denaturing and reducing the insoluble G-CSF protein; and
(f) refolding the G-CSF protein into a biologically active form, wherein the refolded G-CSF protein lacks a non-natural methionine residue and the STII signal sequence.
2. The method of claim 1 further comprising isolating the refolded G-CSF protein.
3. The method of claim 2 , wherein said G-CSF protein is isolated by column chromatography.
4. The method of claim 2 , wherein the isolated G-CSF protein is modified with polyethylene glycol.
5. The method of claim 4 , wherein the polyethylene glycol is a cysteine-reactive polyethylene glycol.
6. The method of claim 2 , wherein the isolated G-CSF protein is modified with a cysteine-reactive moiety.
7. The method of claim 1 , wherein the G-CSF protein is human G-CSF.
8. The method of claim 1 , wherein the E. coli host cell is E. coli W3110.
9. The method of claim 1 , wherein the G-CSF protein is a human G-CSF cysteine mutein.
10. The method of claim 9 , wherein the G-CSF cysteine mutein comprises a cysteine residue substituted for an amino acid selected from the group consisting of T1, P2, L3, A6, S7, W58, A68, E93, A129, Q131, T133, Q134, A136, A139, A141 and Q173.
11. The method of claim 9 , wherein the G-CSF cysteine mutein comprises a cysteine residue added preceding the first amino acid of the mature protein.
12. The method of claim 9 , wherein the G-CSF cysteine mutein comprises a cysteine residue added following the last amino acid of the protein.
13. The method of claim 9 , wherein the G-CSF cysteine mutein comprises a cysteine residue substituted for an amino acid selected from the group consisting of T1, P2, L3, A6 and S7.
14. The method of claim 9 , wherein the G-CSF cysteine mutein comprises a cysteine residue substituted for an amino acid selected from the group consisting of W58, and A68.
15. The method of claim 9 , wherein the G-CSF cysteine mutein comprises a cysteine residue substituted for an amino acid selected from the group consisting of E93 and Q173.
16. The method of claim 9 , wherein the G-CSF cysteine mutein comprises a cysteine residue substituted for an amino acid selected from the group consisting of A129, Q131, T133, Q134, A136 and A139.
17. The method of claim 9 , wherein the G-CSF cysteine mutein comprises a cysteine residue substituted for A141.
18. The method of claim 9 , wherein the G-CSF cysteine mutein comprises a non-cysteine residue substituted for C17.
19. The method of claim 18 , wherein the non-cysteine amino acid substituted for C17 is serine.