Donnelly Centre, University of Toronto, Toronto, Ontario, Canada.
Nat Chem Biol. 2013 Sep;9(9):565-72. doi: 10.1038/nchembio.1293. Epub 2013 Jul 7.
ATP-binding cassette (ABC) transporters are a ubiquitous class of integral membrane proteins of immense clinical interest because of their strong association with human disease and pharmacology. To improve our understanding of these proteins, we used membrane yeast two-hybrid technology to map the protein interactome of all of the nonmitochondrial ABC transporters in the model organism Saccharomyces cerevisiae and combined this data with previously reported yeast ABC transporter interactions in the BioGRID database to generate a comprehensive, integrated 'interactome'. We show that ABC transporters physically associate with proteins involved in an unexpectedly diverse range of functions. We specifically examine the importance of the physical interactions of ABC transporters in both the regulation of one another and in the modulation of proteins involved in zinc homeostasis. The interaction network presented here will be a powerful resource for increasing our fundamental understanding of the cellular role and regulation of ABC transporters.
三磷酸腺苷结合盒(ABC)转运蛋白是一类普遍存在的完整膜蛋白,具有重要的临床意义,因为它们与人类疾病和药理学密切相关。为了更好地了解这些蛋白质,我们利用膜酵母双杂交技术绘制了模式生物酿酒酵母中非线粒体 ABC 转运蛋白的蛋白质互作组图谱,并将这些数据与之前在 BioGRID 数据库中报道的酵母 ABC 转运蛋白相互作用结合起来,生成了一个全面的、综合的“互作组”。我们发现 ABC 转运蛋白与参与各种功能的蛋白质有物理关联。我们特别研究了 ABC 转运蛋白之间的物理相互作用在彼此调控以及在调节锌稳态相关蛋白中的重要性。这里呈现的互作网络将成为一个强大的资源,有助于我们深入了解 ABC 转运蛋白的细胞作用和调控机制。