Shi Lichi, Peng Xiaohu, Ahmed Mumdooh A M, Edwards Dale, Brown Leonid S, Ladizhansky Vladimir
Department of Physics and Biophysics Interdepartmental Group, University of Guelph, 50 Stone Road East, Guelph, ON, Canada N1G 2W1.
J Biomol NMR. 2008 May;41(1):9-15. doi: 10.1007/s10858-008-9233-7. Epub 2008 Apr 11.
We describe a simple protocol to achieve homonuclear J-decoupling in the indirect dimensions of multidimensional experiments, and to enhance spectral resolution of the backbone Calpha carbons in the 3D NCACX experiment. In the proposed protocol, the refocusing of the Calpha-CO homonuclear J-couplings is achieved by applying an off-resonance selective pi pulse to the CO spectral region in the middle of Calpha chemical shift evolution. As is commonly used in solution NMR, a compensatory echo period is used to refocus the unwanted chemical shift evolution of Calpha spins, which takes place during the off-resonance selective pulse. The experiments were carried out on the beta1 immunoglobulin binding domain of protein G (GB1). In GB1, such implementation results in significantly reduced line widths, and leads to an overall sensitivity enhancement.
我们描述了一种简单的方法,可在多维实验的间接维度中实现同核J去耦,并提高三维NCACX实验中主链Cα碳的光谱分辨率。在所提出的方法中,通过在Cα化学位移演化过程中对CO光谱区域施加失谐选择性π脉冲来实现Cα-CO同核J耦合的重聚焦。正如在溶液核磁共振中常用的那样,使用一个补偿回波期来重聚焦Cα自旋在失谐选择性脉冲期间发生的不需要的化学位移演化。实验是在蛋白G(GB1)的β1免疫球蛋白结合结构域上进行的。在GB1中,这种方法可显著减小线宽,并导致整体灵敏度提高。