๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Removal of endotoxin from protein solutions by phase separation using triton X-114

โœ Scribed by Yoshitomi Aida; Michael J. Pabst


Book ID
118011419
Publisher
Elsevier Science
Year
1990
Tongue
English
Weight
359 KB
Volume
132
Category
Article
ISSN
0022-1759

No coin nor oath required. For personal study only.

โœฆ Synopsis


Endotoxin contamination of protein solutions was reduced by a phase separation technique using the detergent, Triton X-114. Protein solutions containing endotoxin were treated with Triton X-114 on ice. The solution was then warmed to 37ยฐC, whereupon two phases formed. The Triton X-114 phase, containing the endotoxin, was precipitated by centrifugation. The first cycle of phase separation produced a 1000-fold reduction of endotoxin from contaminated preparations of cytochrome c, catalase and albumin. Complete removal of endotoxin could be achieved by further cycles of phase separation. Each cycle of phase separation resulted in only a 2% loss of protein, and could be completed within 15 rain. The small amount of detergent (0.018%) that persisted in protein solution could be removed by gel filtration or absorption. Proteins treated by this procedure retained normal functions. This phase separation technique provides a rapid and gentle method for removing endotoxin from protein solutions.


๐Ÿ“œ SIMILAR VOLUMES


Phase separation of rat intestinal brush
โœ Chinnaswamy Tiruppathi; David H. Alpers; Bellur Seetharam ๐Ÿ“‚ Article ๐Ÿ“… 1986 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 901 KB

Rat intestinal microvillus membrane contains at least 24 polypeptides, of which 18 can be solubilized using Triton X-114 at 4 degrees C. Upon phase separation at 32 degrees C, 11 proteins separated nearly completely into the detergent-rich phase, while 9 proteins were found exclusively in the aqueou

Phase separation temperatures of mixture
โœ Barry R. Ganong; John P. Delmore ๐Ÿ“‚ Article ๐Ÿ“… 1991 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 333 KB

Triton X-114 solutions separate above 22 degrees C into two immiscible aqueous phases. The more dense phase is enriched in detergent, and the less dense phase is depleted of detergent, relative to the original single phase. This phenomenon has been used to partition proteins according to hydrophobic