Legault P, Li J, Mogridge J, Kay L E, Greenblatt J
Banting and Best Department of Medical Research, University of Toronto, Ontario, Canada.
Cell. 1998 Apr 17;93(2):289-99. doi: 10.1016/s0092-8674(00)81579-2.
The structure of the complex formed by the arginine-rich motif of the transcriptional antitermination protein N of phage lambda and boxB RNA was determined by heteronuclear magnetic resonance spectroscopy. A bent alpha helix in N recognizes primarily the shape and negatively charged surface of the boxB hairpin through multiple hydrophobic and ionic interactions. The GAAGA boxB loop forms a GNRA fold, previously described for tetraloops, which is essential for N binding. The fourth nucleotide of the loop extrudes from the GNRA fold to enable the E. coli elongation factor NusA to recognize the N protein/RNA complex. This structure reveals a new mode of RNA-protein recognition and shows how a small RNA element can facilitate a protein-protein interaction and thereby nucleate formation of a large ribonucleoprotein complex.
通过异核磁共振光谱法确定了噬菌体λ转录抗终止蛋白N富含精氨酸的基序与boxB RNA形成的复合物的结构。N中一个弯曲的α螺旋主要通过多种疏水和离子相互作用识别boxB发夹的形状和带负电荷的表面。GAAGA boxB环形成了一种GNRA折叠,这是先前针对四环描述的,对N的结合至关重要。环的第四个核苷酸从GNRA折叠中伸出,以使大肠杆菌延伸因子NusA能够识别N蛋白/RN A复合物。这种结构揭示了一种新的RNA - 蛋白质识别模式,并展示了一个小的RNA元件如何促进蛋白质 - 蛋白质相互作用,从而促使形成大型核糖核蛋白复合物。