Tan S, Richmond T J
ETH-Zurich, Institut für Molekularbiologie und Biophysik, Switzerland.
Nature. 1998 Feb 12;391(6668):660-6. doi: 10.1038/35563.
The structure of a complex containing the homeodomain repressor protein MATalpha2 and the MADS-box transcription factor MCM1 bound to DNA has been determined by X-ray crystallography at 2.25 A resolution. It reveals the protein-protein interactions responsible for cooperative binding of MATalpha2 and MCM1 to DNA. The otherwise flexible amino-terminal extension of the MATalpha2 homeodomain forms a beta-hairpin that grips the MCM1 surface through parallel beta-strand hydrogen bonds and close-packed, predominantly hydrophobic, side chains. DNA bending induced by MCM1 brings the two proteins closer together, facilitating their interaction. An unusual feature of the complex is that an eight-amino-acid sequence adopts an alpha-helical conformation in one of two copies of the MATalpha2 monomer and a beta-strand conformation in the other. This 'chameleon' sequence of MATalpha2 may be important for recognizing natural operator sites.
通过X射线晶体学以2.25埃的分辨率确定了一种复合物的结构,该复合物包含与DNA结合的同源结构域阻遏蛋白MATalpha2和MADS盒转录因子MCM1。它揭示了负责MATalpha2和MCM1协同结合DNA的蛋白质-蛋白质相互作用。MATalpha2同源结构域原本灵活的氨基末端延伸形成一个β-发夹结构,通过平行β-链氢键和紧密堆积的、主要为疏水的侧链与MCM1表面结合。MCM1诱导的DNA弯曲使这两种蛋白质靠得更近,促进了它们之间的相互作用。该复合物的一个不寻常特征是,在MATalpha2单体的两个拷贝中,一个拷贝中的八氨基酸序列采用α-螺旋构象,另一个拷贝中的八氨基酸序列采用β-链构象。MATalpha2的这种“变色龙”序列可能对识别天然操纵位点很重要。