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Measurement of Ligand-Target Residence Times by H-1 Relaxation Dispersion NMR Spectroscopy

机译:通过H-1弛豫分散NMR光谱测量配体-靶标停留时间

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摘要

A ligand-observed H-1 NMR relaxation experiment is introduced for measuring the binding kinetics of low molecular-weight compounds to their biomolecular targets. We show that this approach, which does not require any isotope labeling, is applicable to ligand target systems involving proteins and nucleic acids of variable molecular size. The experiment is particularly useful for the systematic investigation of low affinity molecules with residence times in the micro- to millisecond time regime.
机译:引入配体观察的H-1 NMR弛豫实验,以测量低分子量化合物与其生物分子靶标的结合动力学。我们表明,这种方法不需要任何同位素标记,适用于涉及可变分子大小的蛋白质和核酸的配体靶标系统。该实验对于系统性研究具有微秒至毫秒时间范围内停留时间的低亲和力分子特别有用。

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