Nicastro Giuseppe, Candel Adela M, Uhl Michael, Oregioni Alain, Hollingworth David, Backofen Rolf, Martin Stephen R, Ramos Andres
Macromolecular Structure Laboratory, The Francis Crick Institute, London NW1 1AT, UK.
At the former MRC National Institute for Medical Research, Mill Hill, London.
Cell Rep. 2017 Jan 31;18(5):1187-1199. doi: 10.1016/j.celrep.2016.12.091.
Zipcode binding protein 1 (ZBP1) is an oncofetal RNA-binding protein that mediates the transport and local translation of β-actin mRNA by the KH3-KH4 di-domain, which is essential for neuronal development. The high-resolution structures of KH3-KH4 with their respective target sequences show that KH4 recognizes a non-canonical GGA sequence via an enlarged and dynamic hydrophobic groove, whereas KH3 binding to a core CA sequence occurs with low specificity. A data-informed kinetic simulation of the two-step binding reaction reveals that the overall reaction is driven by the second binding event and that the moderate affinities of the individual interactions favor RNA looping. Furthermore, the concentration of ZBP1, but not of the target RNA, modulates the interaction, which explains the functional significance of enhanced ZBP1 expression during embryonic development.
邮政编码结合蛋白1(ZBP1)是一种癌胚RNA结合蛋白,它通过KH3-KH4双结构域介导β-肌动蛋白mRNA的转运和局部翻译,这对神经元发育至关重要。KH3-KH4与其各自靶序列的高分辨率结构表明,KH4通过一个扩大的动态疏水凹槽识别非规范的GGA序列,而KH3与核心CA序列的结合特异性较低。对两步结合反应的数据驱动动力学模拟表明,整体反应由第二次结合事件驱动,且各个相互作用的适度亲和力有利于RNA环化。此外,ZBP1的浓度而非靶RNA的浓度调节这种相互作用,这解释了胚胎发育过程中ZBP1表达增强的功能意义。