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过氧化物酶体ABC转运蛋白家族。

The peroxisomal ABC transporter family.

作者信息

Wanders Ronald J A, Visser Wouter F, van Roermund Carlo W T, Kemp Stephan, Waterham Hans R

机构信息

Department of Clinical Chemistry and Pediatrics, Emma Children's Hospital, Laboratory Genetic Metabolic Diseases, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.

出版信息

Pflugers Arch. 2007 Feb;453(5):719-34. doi: 10.1007/s00424-006-0142-x. Epub 2006 Oct 13.

Abstract

This review describes the current state of knowledge about the ABCD family of peroxisomal half adenosine-triphosphate-binding cassette (ABC) transporters. ABCDs are predicted to be present in a variety of eukaryotic organisms, although at present, only ABCDs in the yeast Saccharomyces cerevisiae, the plant Arabidopsis thaliana, and different mammalian species have been identified and characterized to any significant extent. The functional role of none of these ABCDs has been established definitively and awaits successful reconstitution of ABCDs, either as homo- or heterodimers into liposomes, followed by transport studies. Data obtained in S. cerevisiae suggest that the two ABCDs, which have been identified in this organism, form a heterodimer, which actually transports acyl coenzyme A esters across the peroxisomal membrane. In mammals, four ABCDs have been identified, of which one [adrenoleukodystrophy protein (ALDP)] has been implicated in the transport of the coenzyme A esters of very-long-chain fatty acids. Mutations in the gene (ABCD1) encoding ALDP are the cause of a severe X-linked disease, called X-linked adrenoleukodystrophy. The availability of mutant mice in which Abcd1, Abcd2, or Abcd3 have been disrupted will help to resolve the true role of the peroxisomal half-ABC transporters.

摘要

本综述描述了关于过氧化物酶体半腺苷三磷酸结合盒(ABC)转运蛋白ABCD家族的当前知识状态。预计ABCD存在于多种真核生物中,尽管目前仅在酿酒酵母、拟南芥和不同哺乳动物物种中的ABCD得到了一定程度的鉴定和表征。这些ABCD的功能作用尚未明确确立,有待将ABCD以同二聚体或异二聚体形式成功重组到脂质体中,随后进行转运研究。在酿酒酵母中获得的数据表明,在该生物体中鉴定出的两种ABCD形成异二聚体,实际上负责将酰基辅酶A酯转运过过氧化物酶体膜。在哺乳动物中,已鉴定出四种ABCD,其中一种[肾上腺脑白质营养不良蛋白(ALDP)]与超长链脂肪酸的辅酶A酯的转运有关。编码ALDP的基因(ABCD1)中的突变是一种严重的X连锁疾病——X连锁肾上腺脑白质营养不良的病因。已破坏Abcd1、Abcd2或Abcd3的突变小鼠的出现将有助于阐明过氧化物酶体半ABC转运蛋白的真正作用。

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