Nolis Pau, Parella Teodor
Servei RMN, Facultat de Ciències, Universitat Autònoma de Barcelona, E-08193 Bellaterra, Barcelona, Spain.
J Magn Reson. 2005 Sep;176(1):15-26. doi: 10.1016/j.jmr.2005.05.007.
Simple modifications of the sensitivity-improved HSQC-TOCSY pulse sequence are proposed for the easy determination of the sign and the magnitude of homonuclear and heteronuclear coupling constants. Whereas in well-resolved regions, a clean two-component E.COSY-like pattern allows a direct measurement from a single 2D spectrum, separate acquisition of equivalent single-component TROSY/anti-TROSY spectra becomes highly interesting when spectral crowding complicates the spectral analysis. It is also demonstrated that an additional restricted planar mixing element after the isotropic TOCSY process completely retains all spin-editing features and permits the accurate measurement of the sign and the size of the corresponding homonuclear proton-proton coupling constants. Among others, the proposed techniques are particularly suited for molecules presenting a great number of CH and NH spin systems. Examples and practical details of the implementation of these techniques on standard carbohydrates and peptides at 13C and 15N natural abundance are provided.
为便于确定同核和异核耦合常数的符号及大小,提出了对灵敏度提高的HSQC - TOCSY脉冲序列的简单修改。在分辨率良好的区域,清晰的双组分类E.COSY模式允许从单个二维谱直接测量,而当光谱拥挤使光谱分析变得复杂时,单独采集等效的单组分TROSY/反TROSY谱就变得非常有意义。还证明了在各向同性TOCSY过程之后添加一个额外的受限平面混合元件可完全保留所有自旋编辑特征,并允许准确测量相应同核质子 - 质子耦合常数的符号和大小。其中,所提出的技术特别适用于具有大量CH和NH自旋系统的分子。提供了在13C和15N天然丰度下将这些技术应用于标准碳水化合物和肽的示例及实际细节。