Institute of Molecular Biology, Academia Sinica, Taipei 115, Taiwan.
J Biol Chem. 2012 Feb 10;287(7):4783-9. doi: 10.1074/jbc.M111.318329. Epub 2011 Dec 21.
Recent work has uncovered the "GET system," which is responsible for endoplasmic reticulum targeting of tail-anchored proteins. Although structural information and the individual roles of most components of this system have been defined, the interactions and interplay between them remain to be elucidated. Here, we investigated the interactions between Get3 and the Get4-Get5 complex from Saccharomyces cerevisiae. We show that Get3 interacts with Get4-Get5 via an interface dominated by electrostatic forces. Using isothermal titration calorimetry and small-angle x-ray scattering, we further demonstrate that the Get3 homodimer interacts with two copies of the Get4-Get5 complex to form an extended conformation in solution.
最近的研究揭示了“GET 系统”,该系统负责尾部锚定蛋白的内质网靶向。尽管已经确定了该系统的大多数组件的结构信息和个别作用,但它们之间的相互作用和相互作用仍有待阐明。在这里,我们研究了酿酒酵母中 Get3 和 Get4-Get5 复合物之间的相互作用。我们表明,Get3 通过主要由静电相互作用控制的界面与 Get4-Get5 相互作用。使用等温滴定量热法和小角 X 射线散射,我们进一步证明 Get3 同源二聚体与两个 Get4-Get5 复合物相互作用,在溶液中形成延伸构象。