| Literature DB >> 15862354 |
Sabata Martino1, Antonella Consiglio, Cristina Cavalieri, Roberto Tiribuzi, Egidia Costanzi, Giovanni Maria Severini, Carla Emiliani, Claudio Bordignon, Aldo Orlacchio.
Abstract
The production of active Arylsulfatase A is a key step in the development of enzyme replacement therapy for Metachromatic Leukodystrophy. To obtain large amounts of purified Arylsulfatase A for therapeutic use, we combined a retroviral expression system with a versatile and rapid purification protocol that can easily and reliably be adapted to high-throughput applications. The purification method consists of an initial ion-exchange DEAE-cellulose chromatography step followed by immuno-affinity purification using a polyclonal antibody against a 29-mer peptide of the Arylsulfatase A sequence. Immuno-adsorbed protein was eluted with a combination of acidic pH and an optimal concentration of the 29-mer peptide. This protocol reproducibly yielded approximately 100 microg of >99% pure human Arylsulfatase A, corresponding to 152 mU of enzyme activity, per liter of culture medium with properties similar to those of human non-recombinant protein.Entities:
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Year: 2005 PMID: 15862354 DOI: 10.1016/j.jbiotec.2005.01.018
Source DB: PubMed Journal: J Biotechnol ISSN: 0168-1656 Impact factor: 3.307