期刊
JOURNAL OF BIOMOLECULAR NMR
卷 34, 期 2, 页码 63-73出版社
SPRINGER
DOI: 10.1007/s10858-005-5359-z
关键词
C-13 & N-15 direct detection; NMR spectroscopy; paramagnetic NMR; pseudo-contact shifts; sequence specific assignment; solution structure determination
Paramagnetic proteins generally contain regions with diverse relaxation properties. Nuclei in regions far from the metal center may behave like those in diamagnetic proteins, but those closer to the metal experience rapid relaxation with accompanying line broadening. We have used a set of NMR experiments optimized to capture data from these various concentric regions in assigning the signals from a paramagnetic Calbindin D-9K derivative in which one of the two calcium ions has been replaced by thulium(III). Normal double- and triple-resonance experiments with H-1 detection were used in collecting data from nuclei in the diamagnetic-like region; these approaches identified signals from fewer than 50% of the amino acid residues (those with d > 17.5 angstrom from thulium(III)). Paramagnetism-optimized two-dimensional NMR experiments with H-1 detection were used in collecting data from nuclei in the next nearer region (d > 15 angstrom). Standard (d > 14 angstrom) and optimized (d > 9 angstrom) C-13 direct-detection experiments were used to capture data from nuclei in the next layer. Finally nuclei closest to the metal were detected by one-dimensional C-13 (d > 5 angstrom) and one-dimensional N-15 data collection (d > 4.2 angstrom). NMR signals were assigned on the basis of through-bond correlations and, for signals closest to the metal, pseudocontact shifts. The latter were determined from chemical shift differences between assigned signals in thulium(III) and lanthanum(III) derivatives of Calbindin D-9K and they were interpreted on the basis of a structural model for the lanthanide-substituted protein. This approach yielded assignments of at least one resonance per amino acid residue, including those in the thulium(III) coordination sphere.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据