Tailoring broadband inversion pulses for MAS solid state NMR

被引:8
作者
Riedel, Kerstin [1 ]
Herbst, Christian [1 ]
Leppert, Joerg [1 ]
Ohlenschlaeger, Oliver [1 ]
Goerlach, Matthias [1 ]
Ramachandran, Ramadurai [1 ]
机构
[1] Fritz Lipmann Inst, Leibniz Inst Age Res, Res Grp Mol Biophys, NMR Spect, D-07745 Jena, Germany
关键词
double-quantum spectroscopy; inversion pulses; MAS; solid state NMR;
D O I
10.1007/s10858-006-9044-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A simple approach is demonstrated for designing optimised broadband inversion pulses for MAS solid state NMR studies of biological systems. The method involves a two step numerical optimisation procedure and takes into account experimental requirements such as the pulse length, resonance offset range and extent of H-1 inhomogeneity compensation needed. A simulated annealing protocol is used initially to find appropriate values for the parameters that define the well known tanh/tan adiabatic pulse such that a satisfactory spin inversion is achieved with minimum RF field strength. This information is then used in the subsequent stage of refinement where the RF pulse characteristics are further tailored via a local optimisation procedure without imposing any restrictions on the amplitude and frequency modulation profiles. We demonstrate that this approach constitutes a generally applicable tool for obtaining pulses with good inversion characteristics. At moderate MAS frequencies the efficacy of the method is experimentally demonstrated for generating double-quantum NMR spectra via the zero-quantum dipolar recoupling scheme RFDR.
引用
收藏
页码:275 / 283
页数:9
相关论文
共 33 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]   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
[3]   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
[4]  
BENNETT AE, 1994, NMR-B PR PR, V33, P1
[5]   Determination of polypeptide backbone dihedral angles in solid state NMR by double quantum 13C chemical shift anisotropy measurements [J].
Blanco, FJ ;
Tycko, R .
JOURNAL OF MAGNETIC RESONANCE, 2001, 149 (01) :131-138
[6]   Symmetry principles in the nuclear magnetic resonance of spinning solids: Heteronuclear recoupling by generalized Hartmann-Hahn sequences [J].
Brinkmann, A ;
Levitt, MH .
JOURNAL OF CHEMICAL PHYSICS, 2001, 115 (01) :357-384
[7]   Symmetry principles for the design of radiofrequency pulse sequences in the nuclear magnetic resonance of rotating solids [J].
Carravetta, M ;
Edén, M ;
Zhao, X ;
Brinkmann, A ;
Levitt, MH .
CHEMICAL PHYSICS LETTERS, 2000, 321 (3-4) :205-215
[8]  
DAM LV, 2002, BIOPHYS J, V83, P2835
[9]   Dipolar recoupling under magic-angle spinning conditions [J].
Dusold, S ;
Sebald, A .
ANNUAL REPORTS ON NMR SPECTROSCOPY, VOL 41, 2000, 41 :185-264
[10]   Dipolar recoupling in MAS spectra of biological solids [J].
Griffin, RG .
NATURE STRUCTURAL BIOLOGY, 1998, 5 (Suppl 7) :508-512