Pawloski Westley, Gruschus James M, Opina Ana, Vasalatiy Olga, Tjandra Nico
Biochemistry and Biophysics Center, National Heart, Lung, and Blood Institute, National Institutes of Health, 50 South Drive, Room 3503, Bethesda, MD, 20892, USA.
Chemistry and Synthesis Center, National Heart, Lung, and Blood Institute, National Institutes of Health, Rockville, MD, 20850, USA.
J Biomol NMR. 2025 Apr 10. doi: 10.1007/s10858-025-00468-9.
Paramagnetic relaxation enhancement (PRE) is widely used in biomolecular NMR spectroscopy to obtain long-range distance and orientational information for intra- or intermolecular interactions. In contrast to conventional PRE measurements, which require tethering small molecules containing either a radical or paramagnetic ion to specific sites on the target protein, solvent PRE (sPRE) experiments utilize paramagnetic cosolutes to induce a delocalized PRE effect. Compounds developed as contrast agents in magnetic resonance imaging (MRI) applications typically consist of Gd chelated by a small molecule. Coordinating these Gd-containing small molecules to larger and inert scaffolds has been shown to increase the PRE-effect and produce more effective contrast agents in MRI. Inspired by their use as MRI contrast agent, in this work we evaluate the effectiveness of using a functionalized polyamidoamine (PAMAM) dendrimer for sPRE measurements. Using ubiquitin as a model system, we measured the sPRE effect from a generation 5 PAMAM dendrimer (G5-Gd) as a function of temperature and pH and compared to conventional relaxation agents. We also demonstrated the utility of G5-Gd in sPRE studies to monitor changes in the structures of two proteins as they bind their ligands. These studies highlight the attractive properties of these macromolecular relaxation agents in biomolecular sPRE.
顺磁弛豫增强(PRE)在生物分子核磁共振光谱中被广泛应用,以获取分子内或分子间相互作用的远程距离和取向信息。与传统的PRE测量不同,传统PRE测量需要将含有自由基或顺磁性离子的小分子连接到目标蛋白质上的特定位点,溶剂PRE(sPRE)实验利用顺磁性共溶质来诱导离域的PRE效应。在磁共振成像(MRI)应用中作为造影剂开发的化合物通常由小分子螯合的钆组成。已证明将这些含钆小分子与更大的惰性支架配位可增强PRE效应,并在MRI中产生更有效的造影剂。受其作为MRI造影剂用途的启发,在这项工作中,我们评估了使用功能化聚酰胺胺(PAMAM)树枝状大分子进行sPRE测量的有效性。以泛素为模型系统,我们测量了第5代PAMAM树枝状大分子(G5-Gd)的sPRE效应随温度和pH的变化,并与传统弛豫剂进行了比较。我们还展示了G5-Gd在sPRE研究中的效用,以监测两种蛋白质在结合其配体时结构的变化。这些研究突出了这些大分子弛豫剂在生物分子sPRE中的诱人特性。