Gruschus J M, Ferretti J A
Laboratory of Biophysical Chemistry, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, 20892, USA.
J Magn Reson. 1998 Nov;135(1):87-92. doi: 10.1006/jmre.1998.1532.
Two pulse sequences are described that employ a modified water flipback technique to enhance the signal intensity of weak side chain resonances at the protein-DNA interface of the vnd/NK-2 homeodomain/DNA complex in an 15N-edited three-dimensional NOESY-HMQC spectrum. The pulse sequences presented employ water flipback pulses at the beginning of the NOESY mixing time, optimizing the direct NOE transfer of magnetization from the water to the protein by maximizing the z-component of the water magnetization. In one of the pulse sequences, radiation damping during the the indirect 1H and 15N evolution times is suppressed. A modified version of the WATERGATE water suppression technique is employed during the HMQC portion of the experiment. The signal enhancement is demonstrated for the resonances of the side chain amide of Asn51, an invariant homeodomain residue whose contact with the DNA is critical for binding. An ancillary advantage of the experiment is the ability to observe NOE transfer of magnetization from water. The information present in the water resonance plane of the three-dimensional spectrum is illustrated in a comparison with the corresponding HMQC spectrum of the protein/DNA complex.
本文描述了两种脉冲序列,它们采用改进的水回波技术,以增强15N编辑的三维NOESY-HMQC谱中vnd/NK-2同源结构域/DNA复合物蛋白质-DNA界面处弱侧链共振的信号强度。所展示的脉冲序列在NOESY混合时间开始时采用水回波脉冲,通过最大化水磁化强度的z分量来优化从水到蛋白质的直接NOE磁化转移。在其中一个脉冲序列中,间接1H和15N演化时间期间的辐射阻尼被抑制。在实验的HMQC部分采用了改进版的WATERGATE水抑制技术。Asn51侧链酰胺的共振信号增强得到了证实,Asn51是同源结构域中的一个不变残基,其与DNA的接触对结合至关重要。该实验的一个附带优势是能够观察到从水的NOE磁化转移。通过与蛋白质/DNA复合物的相应HMQC谱进行比较,展示了三维谱水共振平面中的信息。