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使用13C、15N双标记DNA的核磁共振:带有14聚体DNA双链体的触角足同源异型域复合体。

NMR with 13C, 15N-doubly-labeled DNA: the Antennapedia homeodomain complex with a 14-mer DNA duplex.

作者信息

Fernández C, Szyperski T, Ono A, Iwai H, Tate S, Kainosho M, Wüthrich K

机构信息

Institut für Molekularbiologie und Biophysik, Eidgenössische Technische Hochschule Hönggerberg, Zürich, Switzerland.

出版信息

J Biomol NMR. 1998 Jul;12(1):25-37.

PMID:9729786
Abstract

Nearly complete 1H, 13C and 15N NMR assignments have been obtained for a doubly labeled 14-base pair DNA duplex in solution both in the free state and complexed with the uniformly 15N-labeled Antennapedia homeodomain. The DNA was either fully 13C, 15N-labeled or contained uniformly 13C, 15N-labeled nucleotides only at those positions which form the protein-DNA interface in the previously determined NMR solution structure of the Antennapedia homeodomain-DNA complex. The resonance assignments were obtained in three steps: (i) identification of the deoxyribose spin systems via scalar couplings using 2D and 3D HCCH-COSY and soft-relayed HCCH-COSY; (ii) sequential assignment of the nucleotides via 1H-1H NOEs observed in 3D 13C-resolved NOESY; and (iii) assignment of the imino and amino groups via 1H-1H NOEs and 15N-1H correlation spectroscopy. The assignment of the duplex in the 17 kDa protein-DNA complex was greatly facilitated by the fact that 1H signals of the protein were filtered out in 13C-resolved spectroscopy and by the excellent carbon chemical shift dispersion of the DNA duplex. Comparison of corresponding 13C chemical shifts of the free and the protein-bound DNA indicates conformational changes in the DNA upon complex formation.

摘要

已获得一个双标记的14碱基对DNA双链体在溶液中处于自由状态以及与均匀15N标记的触角足同源域复合时的几乎完整的1H、13C和15N NMR归属。该DNA要么完全被13C、15N标记,要么仅在先前确定的触角足同源域 - DNA复合物的NMR溶液结构中形成蛋白质 - DNA界面的那些位置含有均匀13C、15N标记的核苷酸。共振归属通过三个步骤获得:(i)使用二维和三维HCCH - COSY以及软中继HCCH - COSY通过标量耦合鉴定脱氧核糖自旋系统;(ii)通过在三维13C分辨NOESY中观察到的1H - 1H NOE对核苷酸进行顺序归属;(iii)通过1H - 1H NOE和15N - 1H相关光谱对亚氨基和氨基进行归属。在17 kDa蛋白质 - DNA复合物中双链体的归属因以下事实而大大简化:在13C分辨光谱中蛋白质的1H信号被滤除,以及DNA双链体具有出色的碳化学位移分散性。游离DNA和与蛋白质结合的DNA相应13C化学位移的比较表明复合物形成时DNA的构象变化。

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