Solid-state NMR adiabatic TOBSY sequences provide enhanced sensitivity for multidimensional high-resolution magic-angle-spinning 1H MR spectroscopy

被引:21
作者
Andronesi, Ovidiu C. [1 ,2 ,3 ]
Mintzopoulos, Dionyssios [1 ,2 ,3 ]
Struppe, Jochem [4 ]
Black, Peter M. [5 ]
Tzika, A. Aria [1 ,2 ,3 ]
机构
[1] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Surg,NMR Surg Lab, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Shriners Burn Inst, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Dept Radiol, Athinoula A Martinos Ctr Biomed Imaging, Boston, MA 02114 USA
[4] Bruker BioSpin Corp, Billerica, MA 01821 USA
[5] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Neurosurg, Boston, MA 02115 USA
关键词
Total through bond correlation spectroscopy (TOBSY); Total correlation spescroscopy (TOCSY); high-resolution magic-angle-spinning (HRMAS); adiabatic inversion pulses (AIP); glioblastoma multiforme (GBM);
D O I
10.1016/j.jmr.2008.05.017
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We propose a solid-state NMR method that maximizes the advantages of high-resolution magic-angle-spinning (HRMAS) applied to intact biopsies when compared to more conventional liquid-state NMR approaches. Theoretical treatment, numerical Simulations and experimental results oil intact human brain biopsies are presented. Experimentally, it is proven that an optimized adiabatic TOBSY (TOtal through Bond correlation SpectroscopY) solid-state NMR pulse sequence for two-dimensional H-1-H-1 homonuclear scalar-coupling longitudinal isotropic mixing provides a 20%-50% improvement in signal-to-noise ratio relative to its liquid-state analogue TOCSY (TOtal Correlation SpectroscopY). For this purpose we have refined the C9(15)(1), symmetry-based C-13 TOBSY Pulse sequence for H-1 MRS use and compared it to MLEV-16 TOCSY sequence. Both sequences were rotor-synchronized and implemented using WURST-8 adiabatic inversion pulses. As discussed theoretically and shown in Simulations, the improved magnetization-transfer comes from actively removing residual dipolar Couplings from the average Hamiltonian. Importantly, the solid-state NMR techniques are tailored to perform measurements at low temperatures where sample degradation is reduced. This is the first demonstration of such a concept for HRMAS metabolic profiling of disease processes, including cancer, from biopsies requiring reduced sample degradation for further genomic analysis. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:251 / 258
页数:8
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