CRUK Beatson Institute and Institute of Cancer Sciences, University of Glasgow, Garscube Estate, Switchback Road, Bearsden, Glasgow, G61 1BD, U.K.
Biosci Rep. 2019 Jan 30;39(1). doi: 10.1042/BSR20182219. Print 2019 Jan 31.
Regulated trafficking of internalised integrins and growth factor receptors enables polarisation of morphology and motility and enables lumen formation in multicellular structures. Recycling vesicles marked with Rab11 direct internalised cargo back to the plasma membrane to affect biological processes such as polarised trafficking and cancer cell invasion. A recent study by Ji and colleagues, provides insight into how the trafficking protein Rab11FIP2 links with the actin-based motor myo5b and the small GTPase Rab11 to regulate vesicle tethering and transport along actin filaments [1]. The authors used biochemical methods to demonstrate that Rab11a binds directly to the tail of myo5b and that Rab11FIP2 also forms direct interactions with both Rab11a and myo5b tails. These proteins essentially compete for binding to similar regions and thus can regulate the association and activity of each other. Ji and colleagues further demonstrate that Rab11a activates myo5b by binding to its globular tail and relieving a head-tail autoinhibition. Due to differing affinities between Rab11 and myo5b or Rab11FIP2, they propose that Rab11FIP2 mediates the association of myo5b with cargo vesicles, while Rab11a regulates the motor activity of myo5b. The present study thus elucidates how myo5b is regulated by its interactions with Rab11a and Rab11FIP2 and proposes a model for coordination of recycling vesicle tethering and motor activity. The present study has implications for how cells control polarity and motility in health and disease and suggests how Rab11FIP proteins might control motor protein activity and engagement for transport.
受调控的内吞整合素和生长因子受体的运输使形态和运动发生极化,并使多细胞结构中的管腔形成。用 Rab11 标记的再循环囊泡将内吞货物定向回质膜,以影响生物过程,如极化运输和癌细胞侵袭。最近 Ji 及其同事的一项研究提供了深入了解运输蛋白 Rab11FIP2 如何与基于肌动蛋白的马达蛋白 myo5b 和小 GTPase Rab11 相互作用,从而调节囊泡与肌动蛋白丝的连接和运输[1]。作者使用生化方法证明 Rab11a 直接与 myo5b 的尾部结合,并且 Rab11FIP2 还与 Rab11a 和 myo5b 尾部形成直接相互作用。这些蛋白质本质上竞争结合相似的区域,因此可以调节彼此的结合和活性。Ji 及其同事进一步证明,Rab11a 通过与 myo5b 的球状尾部结合并释放头部-尾部自动抑制来激活 myo5b。由于 Rab11 和 myo5b 或 Rab11FIP2 之间的亲和力不同,他们提出 Rab11FIP2 介导 myo5b 与货物囊泡的结合,而 Rab11a 调节 myo5b 的马达活性。因此,本研究阐明了 myo5b 如何通过与 Rab11a 和 Rab11FIP2 的相互作用来调节,并且提出了一个关于回收囊泡连接和马达活性协调的模型。本研究对于细胞如何在健康和疾病中控制极性和运动具有重要意义,并提出了 Rab11FIP 蛋白如何控制马达蛋白活性和参与运输的问题。