Homonuclear zero-quantum recoupling in fast magic-angle spinning nuclear magnetic resonance

被引:78
作者
Brinkmann, A
Günne, JSAD
Levitt, MH [1 ]
机构
[1] Univ Stockholm, Arrhenius Lab, Div Phys Chem, S-10691 Stockholm, Sweden
[2] Univ Southampton, Dept Chem, Southampton S017 1BJ, Hants, England
关键词
D O I
10.1006/jmre.2002.2525
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Solid-state magic-angle-spinning NMR pulse sequences which implement zero-quantum homonuclear dipolar recoupling are designed with the assistance of symmetry theory. The pulse sequences are compensated on a short time scale by the use of composite pulses and on a longer time scale by the use of supercycles. C-13 dipolar recoupling is demonstrated in powdered organic solids at high spinning frequencies. The new sequences are compared to existing pulse sequences by means of numerical simulations. Experimental two-dimensional magnetization exchange spectra are shown for [U-(13) C]-L-tyrosine. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:79 / 96
页数:18
相关论文
共 87 条
[1]   SIMPSON: A general simulation program for solid-state NMR spectroscopy [J].
Bak, M ;
Rasmussen, JT ;
Nielsen, NC .
JOURNAL OF MAGNETIC RESONANCE, 2000, 147 (02) :296-330
[2]   Probing through-bond connectivities and through-space distances in solids by magic-angle-spinning nuclear magnetic resonance [J].
Baldus, M ;
Iuliucci, RJ ;
Meier, BH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (05) :1121-1124
[3]   Broadband polarization transfer under magic-angle spinning: Application to total through-space-correlation NMR spectroscopy [J].
Baldus, M ;
Meier, BH .
JOURNAL OF MAGNETIC RESONANCE, 1997, 128 (02) :172-193
[4]   BROAD-BAND POLARIZATION-TRANSFER EXPERIMENTS FOR ROTATING SOLIDS [J].
BALDUS, M ;
TOMASELLI, M ;
MEIER, BH ;
ERNST, RR .
CHEMICAL PHYSICS LETTERS, 1994, 230 (4-5) :329-336
[5]   HETERONUCLEAR DECOUPLING IN ROTATING SOLIDS [J].
BENNETT, AE ;
RIENSTRA, CM ;
AUGER, M ;
LAKSHMI, KV ;
GRIFFIN, RG .
JOURNAL OF CHEMICAL PHYSICS, 1995, 103 (16) :6951-6958
[6]   Quantitative conformational measurements in solid state NMR by constant-time homonuclear dipolar recoupling [J].
Bennett, AE ;
Weliky, DP ;
Tycko, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (19) :4897-4898
[7]   Homonuclear radio frequency-driven recoupling in rotating solids [J].
Bennett, AE ;
Rienstra, CM ;
Griffiths, JM ;
Zhen, WG ;
Lansbury, PT ;
Griffin, RG .
JOURNAL OF CHEMICAL PHYSICS, 1998, 108 (22) :9463-9479
[8]   CHEMICAL-SHIFT CORRELATION SPECTROSCOPY IN ROTATING SOLIDS - RADIO FREQUENCY-DRIVEN DIPOLAR RECOUPLING AND LONGITUDINAL EXCHANGE [J].
BENNETT, AE ;
OK, JH ;
GRIFFIN, RG ;
VEGA, S .
JOURNAL OF CHEMICAL PHYSICS, 1992, 96 (11) :8624-8627
[9]  
*BIOMAGRESBANK BMR, 2001, RESTR SET AM AC CHEM
[10]   Quantized field description of rotor frequency-driven dipolar recoupling [J].
Boender, GJ ;
Vega, S ;
de Groot, HJM .
JOURNAL OF CHEMICAL PHYSICS, 2000, 112 (03) :1096-1106