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一种 pH 敏感的、多彩的、镧系元素螯合的顺磁 NMR 探针。

A pH-sensitive, colorful, lanthanide-chelating paramagnetic NMR probe.

机构信息

Gorlaeus Laboratories, Leiden Institute of Chemistry, Leiden University, 2300 RA Leiden, The Netherlands.

出版信息

J Am Chem Soc. 2012 Oct 17;134(41):17306-13. doi: 10.1021/ja307824e. Epub 2012 Oct 5.

DOI:10.1021/ja307824e
PMID:22994925
Abstract

Paramagnetic lanthanides ions are broadly used in NMR spectroscopy. The effects of unpaired electrons on NMR spectral parameters provide a powerful tool for the characterization of macromolecular structures and dynamics. Here, a new lanthanide-chelating NMR probe, Caged Lanthanide NMR Probe-7 (CLaNP-7), is presented. It can be attached to protein surfaces via two disulfide bridges, yielding a probe that is rigid relative to the protein backbone. CLaNP-7 extends the application range of available probes. It has a yellow color, which is helpful for sample preparation. Its effects are comparable to those of CLaNP-5, but its charge is two units lower (+1) than that of CLaNP-5 (+3), reducing the change in surface potential after probe attachment. It also has a different magnetic susceptibility tensor, so by using both tags, two sets of structural restraints can be obtained per engineered cysteine pair. Moreover, it was found that the orientation of the magnetic susceptibility tensor is pH dependent (pK(a) ≈ 7) when a histidine residue is located in the neighborhood of the probe attachment site. The results show that the His imidazole group interacts with the CLaNP-7 tag. It is proposed that the histidine residue forms a hydrogen bond to a water/hydroxyl molecule that occupies the ninth coordination position on the lanthanide, thus breaking the two-fold symmetry of the CLaNP tag in a pH-dependent way.

摘要

顺磁镧系元素离子广泛应用于 NMR 光谱学。不成对电子对 NMR 光谱参数的影响为研究大分子结构和动力学提供了强有力的工具。本研究介绍了一种新的镧系螯合 NMR 探针 Caged Lanthanide NMR Probe-7(CLaNP-7)。它可以通过两个二硫键连接到蛋白质表面,从而得到与蛋白质主链相对刚性的探针。CLaNP-7 扩展了现有探针的应用范围。它具有黄色,这有助于样品制备。其效果可与 CLaNP-5 相媲美,但它的电荷比 CLaNP-5 低两个单位(+1)(CLaNP-5 为+3),减少了探针连接后表面电势的变化。它还具有不同的磁各向异性张量,因此,通过使用两种标签,可以从每个工程半胱氨酸对获得两组结构约束。此外,当组氨酸残基位于探针连接位点附近时,发现磁各向异性张量的取向随 pH 值变化(pK(a)≈7)。结果表明,组氨酸咪唑基团与 CLaNP-7 标签相互作用。据推测,组氨酸残基与占据镧系元素第九配位位置的水/羟基分子形成氢键,从而以 pH 依赖的方式打破 CLaNP 标签的二面体对称性。

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