Li Hong-Ye, Chye Mee-Len
Department of Botany, The University of Hong Kong, Pokfulam Road, Hong Kong, China.
Plant Mol Biol. 2003 Mar;51(4):483-92. doi: 10.1023/a:1022330304402.
Cytosolic acyl-CoA binding proteins bind long-chain acyl-CoAs and act as intracellular acyl-CoA transporters and pool formers. Recently, we have characterized Arabidopsis thaliana cDNAs encoding novel forms of ACBP, designated ACBP1 and ACBP2, that contain a hydrophobic domain at the N-terminus and show conservation at the acyl-CoA binding domain to cytosolic ACBPs. We have previously demonstrated that ACBP1 is membrane-associated in Arabidopsis. Here, western blot analysis of anti-ACBP2 antibodies on A. thaliana protein showed that ACBP2 is located in the microsome-containing membrane fraction and in the subcellular fraction containing large particles (mitochondria, chloroplasts and peroxisomes), resembling the subcellular localization of ACBP1. To further investigate the subcellular localization of ACBP2, we fused ACBP2 translationally in-frame to GFP. By means of particle gene bombardment, ACBP2-GFP and ACBP1-GFP fusion proteins were observed transiently expressed at the plasma membrane and at the endoplasmic reticulum in onion epidermal cells. GFP fusions with deletion derivatives of ACBPI or ACBP2 lacking the transmembrane domain were impaired in membrane targeting. Our investigations also showed that when the transmembrane domain of ACBP1 or that of ACBP2 was fused with GFP, the fusion protein was targeted to the plasma membrane, thereby establishing their role in membrane targeting. The localization of ACBP1-GFP is consistent with our previous observations using immunoelectron microscopy whereby ACBPI was localized to the plasma membrane and vesicles. We conclude that ACBP2, like ACBP1, is a membrane protein that likely functions in membrane-associated acyl-CoA transfer/metabolism.
胞质酰基辅酶A结合蛋白可结合长链酰基辅酶A,并作为细胞内酰基辅酶A转运蛋白和库形成蛋白发挥作用。最近,我们鉴定了拟南芥中编码新型ACBP形式(命名为ACBP1和ACBP2)的cDNA,它们在N端含有一个疏水区,并且在酰基辅酶A结合结构域与胞质ACBP具有保守性。我们之前已经证明ACBP1在拟南芥中与膜相关。在此,用抗ACBP2抗体对拟南芥蛋白进行的蛋白质印迹分析表明,ACBP2位于含微粒体的膜组分以及含有大颗粒(线粒体、叶绿体和过氧化物酶体)的亚细胞组分中,类似于ACBP1的亚细胞定位。为了进一步研究ACBP2的亚细胞定位,我们将ACBP2与GFP进行了框内翻译融合。通过微粒基因轰击,在洋葱表皮细胞中观察到ACBP2 - GFP和ACBP1 - GFP融合蛋白在质膜和内质网上瞬时表达。与缺乏跨膜结构域的ACBPI或ACBP2缺失衍生物的GFP融合体在膜靶向方面受损。我们的研究还表明,当ACBP1或ACBP2的跨膜结构域与GFP融合时,融合蛋白靶向质膜,从而确定了它们在膜靶向中的作用。ACBP1 - GFP的定位与我们之前使用免疫电子显微镜的观察结果一致,据此ACBPI定位于质膜和囊泡。我们得出结论,ACBP2与ACBP1一样,是一种膜蛋白,可能在与膜相关的酰基辅酶A转移/代谢中发挥作用。