Biomolecular ligands screening using radiation damping difference WaterLOGSY spectroscopy

被引:0
作者
Peng Sun
Xianwang Jiang
Bin Jiang
Xu Zhang
Maili Liu
机构
[1] Chinese Academy of Sciences,Wuhan Center for Magnetic Resonance, State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Institute of Physics and Mathematics
[2] University of Chinese Academy of Sciences,undefined
来源
Journal of Biomolecular NMR | 2013年 / 56卷
关键词
NMR; Radiation damping; Ligand screening; WaterLOGSY;
D O I
暂无
中图分类号
学科分类号
摘要
Water-ligand observed via gradient spectroscopy (WaterLOGSY) is a widely used nuclear magnetic resonance method for ligand screening. The crucial procedure for the effectiveness of WaterLOGSY is selective excitation of the water resonance. The selective excitation is conventionally achieved by using long selective pulse, which causes partial saturation of the water magnetization leading to reduction of sensitivity, in addition to time consuming and error prone. Therefore, many improvements have been made to enhance the sensitivity and robustness of the method. Here we propose an alternative selective excitation scheme for WaterLOGSY by utilizing radiation damping effect. The pulse scheme starts simply with a hard inversion pulse, instead of selective pulse or pulse train, followed by a pulse field gradient to control the radiation damping effect. The rest parts of the pulse scheme are similar to conventional WaterLOGSY. When the gradient pulse is applied immediately after the inversion pulse, the radiation damping effect is suppressed, and all of the magnetization is inversed. When the gradient pulse and the inversion pulse are about 10–20 ms apart, the radiation damping effect remains active and drives the water magnetization toward +z-axis, resulting in selective non-inversion of the water magnetization. By taking the differences of the spectra obtained under these two conditions, one should get the result of WaterLOGSY. The method is demonstrated to be simple, robust and sensitive for ligand screening.
引用
收藏
页码:285 / 290
页数:5
相关论文
共 107 条
[1]  
Bai GY(2005)A competitive low-affinity binding model for determining the mutual and specific sites of two ligands on protein J Pharm Biomed Anal 38 588-593
[2]  
Cui YF(1998)Measurement of chemical exchange rate constants with solvent protons using radiation damping J Magn Reson 131 358-361
[3]  
Yang YH(1998)NOE pumping: a novel NMR technique for identification of compounds with binding affinity to macromolecules J Am Chem Soc 120 10258-10259
[4]  
Ye CH(2000)NOE pumping. 2. A high-throughput method to determine compounds with binding affinity to macromolecules by NMR J Am Chem Soc 122 414-415
[5]  
Liu ML(2004)Analysis of competitive binding of ligands to human serum albumin using NMR relaxation measurements J Pharm Biomed Anal 34 247-254
[6]  
Chen JH(2011)A new solvent suppression method via radiation damping effect Chin Phys B 20 118201-68
[7]  
Mao XA(2000)Identification of compounds with binding affinity to proteins via magnetization transfer from bulk water J Biomol NMR 18 65-359
[8]  
Chen AD(2001)WaterLOGSY as a method for primary NMR screening: practical aspects and range of applicability J Biomol NMR 21 349-162
[9]  
Shapiro MJ(2011)Measurement of amide hydrogen exchange rates with the use of radiation damping J Biomol NMR 51 151-97
[10]  
Chen AD(1997)ROESY with water flip back for high-field NMR of biomolecules J Magn Reson 129 93-802