Zhi Hu Jian, Wind Robert A
Pacific Northwest National Laboratory, P.O. Box 999, Richland, WA 99352, USA.
J Magn Reson. 2002 Nov;159(1):92-100. doi: 10.1016/s1090-7807(02)00005-8.
It was recently demonstrated that the nuclear magnetic resonance (NMR) linewidths for stationary biological samples are dictated mainly by magnetic susceptibility gradients, and that phase-altered spinning sideband (PASS) and phase-corrected magic angle turning (PHORMAT) solid-state NMR techniques employing slow and ultra-slow magic angle spinning (MAS) frequencies can be used to overcome the static susceptibility broadening to yield high-resolution, spinning sideband (SSB)-free 1H NMR spectra [Magn. Reson. Med. 46 (2001) 213; 47 (2002) 829]. An additional concern is that molecular diffusion in the presence of the susceptibility gradients may limit the minimum useful MAS frequency by broadening the lines and reducing SSB suppression at low spinning frequencies. In this article the performance of PASS, PHORMAT, total sideband suppression (TOSS), and standard MAS techniques were evaluated as a function of spinning frequency. To this end, 300MHz (7.05T) 1H NMR spectra were acquired via PASS, TOSS, PHORMAT, and standard MAS NMR techniques for a 230-microm-diameter spherical glass bead pack saturated with water. The resulting strong magnetic susceptibility gradients result in a static linewidth of about 3.7kHz that is larger than observed for a natural biological sample, constituting a worst-case scenario for examination of susceptibility broadening effects.
(I) TOSS produces a distorted centerband and fails in suppressing the SSBs at a spinning rate below approximately 1kHz. (II) Standard MAS requires spinning speeds above a few hundred Hz to separate the centerband from the SSBs. (III) PASS produces nearly SSB-free spectra at spinning speeds as low as 30Hz, and is only limited by T(2)-induced signal losses. (IV) With PHORMAT, a SSB-free isotropic projection is obtained at any spinning rate, even at an ultra-slow spinning rate as slow as 1Hz. (V) It is found empirically that the width of the isotropic peak is proportional to F(-x), where F is the spinning frequency, and x=2 for MAS, 0.84 for PASS, and 0.5 for PHORMAT.
最近的研究表明,静止生物样品的核磁共振(NMR)线宽主要由磁化率梯度决定,并且采用慢和超慢魔角旋转(MAS)频率的相改变旋转边带(PASS)和相位校正魔角旋转(PHORMAT)固态NMR技术可用于克服静态磁化率展宽,以产生高分辨率、无旋转边带(SSB)的1H NMR谱[《磁共振医学》46(2001)213;47(2002)829]。另一个问题是,在存在磁化率梯度的情况下分子扩散可能会通过展宽谱线和降低低旋转频率下的SSB抑制来限制最小有用MAS频率。在本文中,评估了PASS、PHORMAT、全边带抑制(TOSS)和标准MAS技术作为旋转频率函数的性能。为此,通过PASS、TOSS、PHORMAT和标准MAS NMR技术,对充满水的直径为230微米的球形玻璃珠包进行了300MHz(7.05T)的1H NMR谱采集。由此产生的强磁化率梯度导致静态线宽约为3.7kHz,这比天然生物样品中观察到的要大,构成了研究磁化率展宽效应的最坏情况。
(I)TOSS产生失真的中心带,并且在低于约1kHz的旋转速率下无法抑制SSB。(II)标准MAS需要几百Hz以上的旋转速度才能将中心带与SSB分开。(III)PASS在低至30Hz的旋转速度下产生几乎无SSB的谱,并且仅受T(2)诱导的信号损失限制。(IV)对于PHORMAT,在任何旋转速率下,甚至在低至1Hz的超慢旋转速率下,都可获得无SSB的各向同性投影。(V)根据经验发现,各向同性峰的宽度与F(-x)成正比,其中F是旋转频率,对于MAS,x = 2;对于PASS,x = 0.84;对于PHORMAT,x = 0.5。