Alkyl-dihydroxyacetone phosphate synthase and dihydroxyacetone phosphate acyltransferase form a protein complex in peroxisomes

被引:31
作者
Biermann, J
Just, WW
Wanders, RJA
van den Bosch, H
机构
[1] Univ Utrecht, Inst Biomembranes, Ctr Biomembranes & Lipid Enzymol, Dept Biochem Lipids, NL-3584 CH Utrecht, Netherlands
[2] Univ Heidelberg, Biochem Ctr, D-6900 Heidelberg, Germany
[3] Univ Amsterdam, Acad Med Ctr, Dept Clin Biochem, NL-1012 WX Amsterdam, Netherlands
[4] Univ Amsterdam, Acad Med Ctr, Dept Pediat, NL-1012 WX Amsterdam, Netherlands
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1999年 / 261卷 / 02期
关键词
alkyl-dihydroxyacetonephophate synthase; dihydroxyacetonephophate-acyltransferase; ether phospholipid; peroxisome; chemical cross-linking;
D O I
10.1046/j.1432-1327.1999.00295.x
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
Dihydroxyacetone phosphate (GrnP) acyltransferase and alkyl-GrnP synthase are the key enzymes involved in the biosynthesis of ether phospholipids. Both enzymes are located on the inside of the peroxisomal membrane. Here we report evidence for a direct interaction between these enzymes obtained by the use of chemical cross-linking. After cross-linking and immunoblot analysis alkyl-GrnP synthase could be detected in a 210-kDa complex which was located entirely on the lumenal side of the peroxisomal membrane. Two-dimensional SDS/PAGE demonstrated that GrnP-acyltransferase is also cross-linked in a 210-kDa complex. Co-immunoprecipitation confirmed that the two enzymes interact, in a heterotrimeric complex. Furthermore, alkyl-GrnP synthase can form a homotrimeric complex in the absence of GrnP-acyltransferase as was demonstrated by immunoblot analysis after cross-linking experiments with either GrnP-acyltransferase deficient human fibroblast homogenates or recombinant (His)(6)-tagged alkyl-GrnP synthase. We conclude that alkyl-GrnP synthase interacts selectively with GrnP-acyltransferase in a heterotrimeric complex and in the absence of GrnP-acyltransferase can also form a homotrimeric complex.
引用
收藏
页码:492 / 499
页数:8
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