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Saturation transfer double-difference NMR spectroscopy using a dual solenoid microcoil difference probe

机译:使用双螺线管微线圈差探针的饱和转移双差NMR光谱

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摘要

An experiment designed to collect a saturation transfer double difference (STDD) NMR spectrum using a solenoid microcoil NMR difference probe is reported. STDD-NMR allows the investigation of ligand-biomolecule binding, with moderate concentration requirements for unlabeled molecular targets and the ability to discern binding events in the presence of non-binding ligands. The NMR difference probe acquires the signals from two different samples at once, and cancels common signals automatically through a mechanism of switching between parallel excitation and serial acquisition of the sample signals. STDD spectra were acquired on a system consisting of human serum albumin and two ligands, octanoic acid and glucose. The non-binding ligand, glucose, was cancelled internally through phase cycling, while the protein signal was subtracted automatically by the difference probe. The proton NMR resonance signal from octanoic acid remained in the double difference spectrum. This work demonstrates that the double difference can be performed both internally and automatically through the utilization of the solenoid microcoil NMR difference probe and STDD-NMR pulse sequence, resulting in a clean signal from the binding ligand with good protein background subtraction and an overall favorable result when compared to the conventional approach.
机译:报道了设计用于使用螺线管微线圈NMR差异探针收集饱和转移双差(STDD)NMR光谱的实验。 STDD-NMR可以研究配体与生物分子的结合,对于未标记的分子靶标具有中等浓度要求,并且能够在存在非结合配体的情况下辨别结合事件。 NMR差值探头一次采集两个不同样品的信号,并通过在样品信号的并行激发和串行采集之间切换的机制自动消除公共信号。 STDD光谱是在由人血清白蛋白和两个配体(辛酸和葡萄糖)组成的系统上获得的。通过相循环在内部取消非结合配体葡萄糖,而差异探针自动减去蛋白质信号。来自辛酸的质子NMR共振信号保留在双差谱中。这项工作表明,通过使用螺线管微线圈NMR差异探针和STDD-NMR脉冲序列,可以在内部和自动执行双重差异,从而产生结合配体的纯净信号,并具有良好的蛋白质背景减除效果,总体效果良好与传统方法相比

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