School of Chemistry, University of New South Wales, Sydney NSW 2052, Australia.
Chemistry. 2010 Mar 22;16(12):3827-32. doi: 10.1002/chem.200902904.
Paramagnetic effects from lanthanide ions present powerful tools for protein studies by nuclear magnetic resonance (NMR) spectroscopy provided that the lanthanide can be site-specifically and rigidly attached to the protein. A new, particularly small and rigid lanthanide-binding tag, 3-mercapto-2,6-pyridinedicarboxylic acid (3MDPA), was synthesized and attached to two different proteins via a disulfide bond. The complexes of the N-terminal domain of the E. coli arginine repressor (ArgN) with seven different paramagnetic lanthanide ions and Co(2+) were analyzed in detail by NMR spectroscopy. The magnetic susceptibility anisotropy (Delta chi) tensors and metal position were determined from pseudocontact shifts. The 3MDPA tag generated very different Delta chi tensor orientations compared to the previously studied 4-mercaptomethyl-DPA tag, making it a highly complementary and useful tool for protein NMR studies.
镧系离子的顺磁效应为通过核磁共振(NMR)光谱研究蛋白质提供了强大的工具,前提是镧系元素可以被特异性和刚性地连接到蛋白质上。本文合成了一种新型的、特别小且刚性的镧系元素结合标签 3-巯基-2,6-吡啶二甲酸(3MDPA),并通过二硫键将其连接到两种不同的蛋白质上。通过 NMR 光谱详细分析了大肠杆菌精氨酸阻遏物(ArgN)N 端结构域与七种不同的顺磁镧系离子和 Co(2+)的复合物。通过赝接触位移确定了磁各向异性(Delta chi)张量和金属位置。与之前研究的 4-巯基甲基-DPA 标签相比,3MDPA 标签产生了非常不同的 Delta chi 张量取向,使其成为蛋白质 NMR 研究的高度互补和有用的工具。