Process for purifying bacterially produced M-CSF

Chemistry: natural resins or derivatives; peptides or proteins; – Proteins – i.e. – more than 100 amino acid residues – Lymphokines – e.g. – interferons – interlukins – etc.

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530412, 530414, 530427, 435 711, 435 712, 435 695, 424 851, C07K 1453, C07K 114, C07K 134, C12P 2102

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active

054667810

ABSTRACT:
A process is described for producing M-CSF from bacteria. It includes: fermentation of bacteria containing M-CSF DNA; harvest of the fractions that contain the M-CSF protein (refractile bodies); primary recovery of the protein; solubilization and denaturation of refractile bodies; M-CSF refolding; purification by column chromatography and other methods; and formulation of the properly refolded M-CSF. This method is advantageous over prior methods in terms of yield and purity.

REFERENCES:
patent: 4572798 (1986-02-01), Koths et al.
patent: 4929700 (1990-05-01), Halenbeck et al.
patent: 5248769 (1993-09-01), Darin
Yamanishi et al. "Renaturation, Purification & Characterization of Human Truncated MLSE Expressed in Escherichia coli" J. Biochem 404-409 1991.
Remingtons Pharmaceutical Scienes 17th Ed. 1985 pp. 1538-1539 "Freeze Drying".
Halenbeck et al "Purification & Characterization of Recombinant Human M-CSF & Generation of a Neutralizing Ab Useful for Western Analysis". J Biotechnol. 8:45-58 1988.
Halenbeck et al. "Renaturation & Purification of Biologically Active Recombinant Human MCSF Expressed in E coli Bio Technology". 7:(7) 1989 pp. 710-715.

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