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Large-scale purification of recombinant human angiostatin.
- Source :
-
Protein expression and purification [Protein Expr Purif] 2000 Nov; Vol. 20 (2), pp. 216-27. - Publication Year :
- 2000
-
Abstract
- A process for the purification of recombinant human angiostatin (rhAngiostatin), produced by Pichia pastoris fermentation operated at the 2000-L scale, is reported. rhAngiostatin was recovered and purified directly from crude fermentation broth by cation exchange expanded bed adsorption chromatography. Anion exchange chromatography, hydroxyapatite chromatography, and hydrophobic interaction chromatography were used for further purification. Full-length rhAngiostatin was separated from rhAngiostatin molecules fragmented by endoproteolysis. On average, 140 g of rhAngiostatin was produced per batch, with an overall yield of 59% (n = 9). The purification process was completed in approximately 48 h and used only inexpensive and nontoxic raw materials. Methods development, process synthesis, and process scale-up data are presented and discussed.<br /> (Copyright 2000 Academic Press.)
- Subjects :
- Ammonium Sulfate metabolism
Angiostatins
Antineoplastic Agents isolation & purification
Chromatography methods
Chromatography, High Pressure Liquid
Durapatite metabolism
Electrophoresis, Polyacrylamide Gel
Humans
Peptide Fragments genetics
Phosphates
Pichia genetics
Plasminogen genetics
Recombinant Proteins biosynthesis
Recombinant Proteins isolation & purification
Reproducibility of Results
Peptide Fragments biosynthesis
Peptide Fragments isolation & purification
Plasminogen biosynthesis
Plasminogen isolation & purification
Subjects
Details
- Language :
- English
- ISSN :
- 1046-5928
- Volume :
- 20
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Protein expression and purification
- Publication Type :
- Academic Journal
- Accession number :
- 11049746
- Full Text :
- https://doi.org/10.1006/prep.2000.1276