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醚磷脂生物合成的拓扑结构。

Topography of ether phospholipid biosynthesis.

作者信息

Hardeman D, van den Bosch H

机构信息

Centre for Biomembranes and Lipid Enzymology, University of Utrecht, The Netherlands.

出版信息

Biochim Biophys Acta. 1989 Nov 6;1006(1):1-8. doi: 10.1016/0005-2760(89)90315-9.

Abstract

The enzyme, dihydroxyacetone-phosphate acyltransferase (DHAP-AT) is localized at the inner surface of the peroxisomal membrane but shows no latency. The product, i.e., acyl-DHAP, is the first lipidic intermediate in ether lipid biosynthesis that is converted by alkyldihydroxyacetone-phosphate synthase into alkyl-DHAP. This step and the reductions of acyl-DHAP and alkyl-DHAP to the glycerol 3-phosphate analogs can still take place in peroxisomes. The further conversions of these intermediates into ether-linked choline or ethanolamine glycerophospholipids or plasmalogens take place in the endoplasmic reticulum. In this paper we describe studies to localize acyl-DHAP in the transversal plane of the peroxisomal membrane. To enable these studies, the usually employed assay conditions for DHAP-AT were modified by omission of BSA and by lowering the temperature and the palmitoyl-CoA concentration. Using these modified conditions, we were able to label peroxisomes with endogenously generated acyl-DHAP, with retention of catalase within the peroxisomal membrane. Endogenously generated acyl-DHAP was rapidly extractable from the outer surface of peroxisomes with BSA at 0 degree C, suggesting that even at this temperature the product was transported very fast across the membrane. Trypsin treatment of peroxisomes did not affect this behaviour. Only after short incubation periods, an increase in the proportion of non-extractable acyl-DHAP was observed. In large unilamellar vesicles made from peroxisomal phospholipids no transmembrane movement of acyl-DHAP was found. Despite the apparently rapid transbilayer movement of acyl-DHAP in the presence of BSA, it could still serve as a substrate for the enzyme alkyl-DHAP synthase, which is also localized at the inner surface of the peroxisomal membrane. In addition it was shown that endogenously generated substrate is used at a higher efficiency compared to exogenously added acyl-DHAP, suggesting a close interaction of the two enzymes in the peroxisomal membrane.

摘要

二羟基丙酮磷酸酰基转移酶(DHAP-AT)这种酶定位于过氧化物酶体膜的内表面,但没有潜伏性。其产物即酰基-DHAP,是醚脂生物合成中的首个脂质中间体,它会被烷基二羟基丙酮磷酸合酶转化为烷基-DHAP。这一步以及酰基-DHAP和烷基-DHAP还原为甘油3-磷酸类似物的过程仍可在过氧化物酶体中发生。这些中间体进一步转化为醚键连接的胆碱或乙醇胺甘油磷脂或缩醛磷脂则发生在内质网中。在本文中,我们描述了将酰基-DHAP定位在过氧化物酶体膜横向平面的研究。为了进行这些研究,通过省略牛血清白蛋白(BSA)以及降低温度和棕榈酰辅酶A浓度,对通常用于DHAP-AT的测定条件进行了修改。使用这些修改后的条件,我们能够用内源性生成的酰基-DHAP标记过氧化物酶体,同时过氧化氢酶保留在过氧化物酶体膜内。在0摄氏度时,用BSA可迅速从过氧化物酶体的外表面提取内源性生成的酰基-DHAP,这表明即使在该温度下,产物也能非常快速地跨膜运输。用过氧化物酶体进行胰蛋白酶处理并不影响这种行为。仅在短时间孵育后,才观察到不可提取的酰基-DHAP比例增加。在用过氧化物酶体磷脂制成的大单层囊泡中,未发现酰基-DHAP的跨膜运动。尽管在存在BSA的情况下酰基-DHAP明显有快速的跨双层运动,但它仍可作为同样定位于过氧化物酶体膜内表面的烷基-DHAP合酶的底物。此外,研究表明,与外源性添加的酰基-DHAP相比,内源性生成的底物使用效率更高,这表明过氧化物酶体膜中的这两种酶存在密切相互作用。

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