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Large-scale purification of recombinant human angiostatin.

Authors :
Shepard SR
Boucher R
Johnston J
Boerner R
Koch G
Madsen JW
Grella D
Sim BK
Schrimsher JL
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.)

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