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核糖体结构研究中的冷冻自旋靶标。

Frozen spin targets in ribosomal structure research.

作者信息

Stuhrmann H B

机构信息

GKSS Forschungszentrum, Geesthacht, Germany.

出版信息

Biochimie. 1991 Jul-Aug;73(7-8):899-910. doi: 10.1016/0300-9084(91)90131-j.

Abstract

Polarized neutron scattering strongly depends on nuclear spin polarisation, particularly on proton spin polarisation. A single proton in a deuterated environment then is as efficient as 10 electrons in X-ray anomalous diffraction. Neutron scattering from the nuclear spin label is controlled by the polarisation of neutron spins and nuclear spins. Pure deuteron spin labels and proton spin labels are created by NMR saturation. We report on results obtained from the large subunit of E. coli ribosomes which have been obtained at the research reactor of GKSS using the polarized target facility developed by CERN. The nuclear spins were oriented with respect to an external field by dynamic nuclear polarisation. Proton spin polarisations of more than 80% were obtained in ribosomes at temperatures below 0.5 K. At T = 130 mK the relaxation time of the polarized target is one month (frozen spin target). Polarized small-angle neutron scattering of the in situ structure of rRNA and the total ribosomal protein (TP) has been determined from the frozen spin targets of the large ribosomal subunit, which has been deuterated in the TP and rRNA respectively. The results agree with those from neutron scattering in H2O/D2O mixtures obtained at room temperature. This is a necessary prerequisite for the planned determination of the in situ structure of individual ribosomal proteins and especially of that of ribosome bound mRNA and tRNAs.

摘要

极化中子散射强烈依赖于核自旋极化,特别是质子自旋极化。在氘化环境中的单个质子在X射线反常衍射中与10个电子的效率相当。来自核自旋标记的中子散射由中子自旋和核自旋的极化控制。纯氘核自旋标记和质子自旋标记通过核磁共振饱和产生。我们报告了从大肠杆菌核糖体大亚基获得的结果,这些结果是在GKSS研究反应堆使用欧洲核子研究组织开发的极化靶设施获得的。通过动态核极化使核自旋相对于外部场取向。在温度低于0.5K时,核糖体中的质子自旋极化率超过80%。在T = 130mK时,极化靶的弛豫时间为一个月(冻结自旋靶)。已分别从大亚基的冻结自旋靶中确定了rRNA原位结构和总核糖体蛋白(TP)的极化小角中子散射,其中大亚基的TP和rRNA已被氘化。结果与在室温下从H2O/D2O混合物中的中子散射获得的结果一致。这是计划确定单个核糖体蛋白原位结构,特别是核糖体结合的mRNA和tRNA原位结构的必要前提。

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