SEQUENTIAL RESONANCE ASSIGNMENTS IN DNA H-1-NMR SPECTRA BY TWO-DIMENSIONAL NOE SPECTROSCOPY
SEQUENTIAL RESONANCE ASSIGNMENTS IN DNA H-1-NMR SPECTRA BY TWO-DIMENSIONAL NOE SPECTROSCOPY
复制标题
二维 NOE 光谱对 DNA H-1-NMR 谱的顺序共振归属
DOI:
10.1021/ja00347a075
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发表时间:
1983
影响因子:
15
通讯作者:
R. Kaptein
中科院分区:
文献类型:
--
作者:
R. Scheek;N. Russo;R. Boelens;R. Kaptein
Figure 1. 360-MHz 2-D NOE spectrum (contour plot) of an equimolar mixture of d (TGAGCGG) and d (CCGCTCA), 5 mM in duplex, in 50 mM phosphate, 0.2 Mkc1, 0.02%(w/v) NaN3, T= 28 C, pH 6.5 (meter reading in 2H20). A (ir/2-il-ir/2-Tm-ir/2-t2)„sequence was used, 10 with a 2-s relaxation delay after each acquisition and 0.2-s mixing time rm. 128 free induction decays of 2048 points were accumulated at 512 f¡ values, using quadrature-phase detection in r2 (±5000 Hz) with the carrier frequency at the low-field side of the spectrum. The pulses and receiver phases were cycled through a 32-step phase programthat keeps intact the pure amplitude modulation, and only real t¡ data were collected. 16 Gaussian multiplication17 and zero-filling preceded Fourier transformation in both dimensions and the symmetrized pure absorption phase spectrum is shown. The drawn lines connect intra-(indicated with a dot) and internucleotide contacts between base protons and sugar HI'protons (1A) or sugar H2'and H2" protons (IB) in the d (TGAGCGG) strand. In Figure 1C the corresponding Hl'-H2', H2"(intranucleotide) cross peaks are indicated. Figure ID shows schematically the HI'resonance positions on the diagonal.