SPECIAL CONSIDERATIONS IN THE PURIFICATION OF THE GM3 GANGLIOSIDE FORMING ENZYME, CMP-SIALIC ACID - LACTOSYLCERAMIDE ALPHA-2-3 SIALYLTRANSFERASE (SAT-1) - SOLUBILIZATION OF SAT-1 WITH LAURYLDIMETHYLAMINE OXIDE

被引:4
|
作者
MELKERSONWATSON, LJ [1 ]
SWEELEY, CC [1 ]
机构
[1] MICHIGAN STATE UNIV,DEPT BIOCHEM,E LANSING,MI 48824
关键词
D O I
10.1016/S0006-291X(05)80188-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lauryldimethylamine oxide (LDAO) was employed in the purification of the GM3 ganglioside forming enzyme, CMP-sialic acid: lactosylceramide α2-3 sialyltransferase (SAT-1) (4). This detergent has advantages over the typically employed Triton detergents in the solubilization and stabilization of this sialyltransferase. Crude protein fractions solubilized from rat liver Golgi by several such detergents are very similar in composition as determined by two-dimensional gel electrophoresis. However, LDAO appears to activate and stabilize SAT-1 activity. It is possible that SAT-1 activation involves the structurally similar hydrophobic moieties and quaternary amino groups of LDAO and phosphatidylcholine. © 1990 Academic Press, Inc.
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页码:165 / 171
页数:7
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