Buchko G W, Tung C S, McAteer K, Isern N G, Spicer L D, Kennedy M A
Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, WA 99352, USA.
Nucleic Acids Res. 2001 Jun 15;29(12):2635-43. doi: 10.1093/nar/29.12.2635.
Recent NMR-based, chemical shift mapping experiments with the minimal DNA-binding domain of XPA (XPA-MBD: M98-F219) suggest that a basic cleft located in the loop-rich subdomain plays a role in DNA-binding. Here, XPA-DNA interactions are further characterized by NMR spectroscopy from the vantage point of the DNA using a single-stranded DNA nonamer, dCCAATAACC (d9). Up to 2.5 molar equivalents of XPA-MBD was titrated into a solution of d9. A subset of (31)P resonances of d9 were observed to broaden and/or shift providing direct evidence that XPA-MBD binds d9 by a mechanism that perturbs the phosphodiester backbone of d9. The interior five residues of d9 broadened and/or shifted before (31)P resonances of phosphate groups at the termini, suggesting that when d9 is bound to XPA-MBD the internal residues assume a correlation time that is characteristic of the molecular weight of the complex while the residues at the termini undergo a fraying motion away from the surface of the protein on a timescale such that the line widths are more characteristic of the molecular weight of ssDNA. A molecular model of the XPA-MBD complex with d9 was calculated based on the (15)N (XPA-MBD) and (31)P (d9) chemical shift mapping studies and on the assumption that electrostatic interactions drive the complex formation. The model shows that a nine residue DNA oligomer fully covers the DNA-binding surface of XPA and that there may be an energetic advantage to binding DNA in the 3'-->5' direction rather than in the 5'-->3' direction (relative to XPA-MBD alpha-helix-3).
最近利用XPA最小DNA结合结构域(XPA-MBD:M98-F219)进行的基于核磁共振的化学位移图谱实验表明,位于富含环的亚结构域中的一个碱性裂隙在DNA结合中发挥作用。在此,从DNA的角度出发,使用单链DNA九聚体dCCAATAACC(d9),通过核磁共振光谱进一步表征XPA与DNA的相互作用。将高达2.5摩尔当量的XPA-MBD滴定到d9溶液中。观察到d9的一部分(31)P共振峰变宽和/或位移,这提供了直接证据,表明XPA-MBD通过一种干扰d9磷酸二酯主链的机制与d9结合。d9内部的五个残基在末端磷酸基团的(31)P共振峰之前变宽和/或位移,这表明当d9与XPA-MBD结合时,内部残基呈现出与复合物分子量特征相符的相关时间,而末端的残基则在一个时间尺度上经历远离蛋白质表面的松散运动,使得线宽更具单链DNA分子量的特征。基于(15)N(XPA-MBD)和(31)P(d9)化学位移图谱研究,并假设静电相互作用驱动复合物形成,计算了XPA-MBD与d9复合物的分子模型。该模型表明,一个九个残基的DNA寡聚物完全覆盖了XPA的DNA结合表面,并且相对于XPA-MBD的α-螺旋-3,以3'→5'方向而非5'→3'方向结合DNA可能具有能量优势。