Research School of Chemistry, Australian National University, Canberra, ACT, Australia.
Chemistry. 2011 Jun 6;17(24):6830-6. doi: 10.1002/chem.201003573. Epub 2011 May 3.
Pseudocontact shifts (PCS) from paramagnetic lanthanide ions present powerful long-range structure restraints for studies of proteins by nuclear magnetic resonance spectroscopy. To elicit PCSs, the lanthanide must be attached site-specifically to the target protein. In addition, it needs to be attached rigidly to avoid averaging of the PCSs due to mobility with respect to the protein and it must not interfere with the function of the protein. Here, we present a dipicolinic acid reagent that spontaneously forms a disulfide bond with thiol groups of accessible cysteine residues. A minimal number of rotatable bonds between the cysteine side chain and the tag helps to minimise mobility. Combined with the small size of the tag and quantitative tagging yields, these features make it a highly attractive tool for generating structure restraints by paramagnetic lanthanides.
假接触位移 (PCS) 来自顺磁镧系元素离子,它们为通过核磁共振波谱学研究蛋白质提供了强大的远程结构约束。为了引出 PCS,镧系元素必须特异性地连接到目标蛋白质上。此外,它需要刚性连接,以避免由于相对于蛋白质的移动而平均化 PCS,并不能干扰蛋白质的功能。在这里,我们提出了一种吡啶二酸试剂,它可以与可及半胱氨酸残基的巯基自发形成二硫键。半胱氨酸侧链和标记物之间的最小数量的旋转键有助于最小化移动性。结合标记物的小尺寸和定量标记物产率,这些特征使其成为通过顺磁镧系元素产生结构约束的极具吸引力的工具。