NR AMEJ
AU Walker,S.G.; Dale,C.J.; Lyddiatt,A.
TI Aqueous two-phase partition of complex protein feedstocks derived from brain tissue homogenates
QU Journal of Chromatography. B, Biomedical Applications 1996 May 17; 680(1-2): 91-6
PT journal article
AB This study describes the application of aqueous two-phase partition using polyethylene glycol (PEG)-potassium phosphate systems for the direct recovery of proteins, and aggregates thereof, from mammalian brain tissue homogenates. Investigation of established methodologies for the purification of prion proteins (PrP) from bovine brain affected with transmissible spongiform encephalopathy (BSE) has identified an alternative purification regime based on aqueous two-phase partition. This circumvents energy-intensive and rate-limiting unit operations of ultracentrifugation conventionally used for isolation of PrP. Selectivity of various PEG-phosphate systems varied inversely with polymer molecular mass. The maximum protein recovery from bovine brain extracts was obtained with systems containing PEG 300. Manipulation of the aqueous environment, to back-extract protein product from the PEG-rich top phase into the phosphate-rich lower phase, enabled integration of ATPS with conventional hydrophobic interaction chromatography (HIC) which selectively removes obdurate contaminating proteins (i.e. ferritin).
MH Animal; Brain Stem/*chemistry; Cattle; Chromatography, Agarose; Comparative Study; Electrophoresis, Polyacrylamide Gel; Ferritin/chemistry; Human; Immune Sera/immunology; Immunoblotting; Peptides/immunology; Phosphates/*chemistry; Polyethylene Glycols/*chemistry; Prion Diseases/physiopathology; Prions/immunology/*isolation & purification; Spectrophotometry, Ultraviolet; Tissue Extracts/*chemistry; Water/*chemistry
AD BBSRC Centre for Biochemical Engineering, School of Chemical Engineering, University of Birmingham, UK
SP englisch
PO Niederlande