An improved purification method for the lysosomal storage disease protein β-glucuronidase produced in CHO cells.

Abstract:

:Human β-glucuronidase (GUS; EC 3.2.1.31) is a lysosomal enzyme that catalyzes the hydrolysis of β-d-glucuronic acid residues from the non-reducing termini of glycosaminoglycans. Impairment in GUS function leads to the metabolic disorder mucopolysaccharidosis type VII, also known as Sly syndrome. We produced GUS from a CHO cell line grown in suspension in a 15 L perfused bioreactor and developed a three step purification procedure that yields ∼99% pure enzyme with a recovery of more than 40%. The method can be completed in two days and has the potential to be integrated into a continuous manufacturing scheme.

journal_name

Protein Expr Purif

authors

Fratz-Berilla EJ,Ketcham SA,Parhiz H,Ashraf M,Madhavarao CN

doi

10.1016/j.pep.2017.07.011

subject

Has Abstract

pub_date

2017-12-01 00:00:00

pages

28-35

eissn

1046-5928

issn

1096-0279

pii

S1046-5928(17)30134-1

journal_volume

140

pub_type

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