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通过核磁共振获得准确的核酸浓度。

Accurate nucleic acid concentrations by nuclear magnetic resonance.

作者信息

Cavaluzzi M J, Kerwood D J, Borer P N

机构信息

Department of Chemistry and Graduate Program in Structural Biology, Biochemistry, and Biophysics, Syracuse University, Syracuse, NY 13244, USA.

出版信息

Anal Biochem. 2002 Sep 15;308(2):373-80. doi: 10.1016/s0003-2697(02)00262-2.

Abstract

Determination of the concentration of biochemical samples often yields values with uncertainties of 10-20% or more. This paper details a protocol for use with 500- to 600-MHz NMR spectrometers to measure approximately 1mM concentrations within +/-1-3% accuracy. With suitable precautions, all compounds have equal NMR "absorption coefficients" for protons. About 2mg of sample are needed for proteins and nucleic acids with MW=5000, although less accurate determinations could be made with smaller amounts. The technique utilizes standardized internal reference reagent compounds, cacodylic acid or 3-(trimethylsilyl)propionic-2,2,3,3-d(4) acid sodium salt. Spectra were signal-averaged using long interpulse delays so that integrals of nonexchangeable protons could be quantified relative to the reference standard. Accurate determinations require careful optimization of the homogeneity of the magnetic field and meticulous attention to sample preparation and spectral processing. The main source of error is usually the accuracy of micropipets. If sample preparation errors could be eliminated, the lower limit of accuracy with the current generation of NMR spectrometers is probably near 0.4%. However, this would require >99.5% sample purity. Methods are described to establish the concentration of the standards, and applications are illustrated with DNA mono- and oligonucleotides. Similar procedures should apply to proteins, polysaccharides, and other biomolecules, with about the same accuracy and precision.

摘要

生化样品浓度的测定结果往往具有10%-20%或更高的不确定性。本文详细介绍了一种适用于500-600兆赫核磁共振光谱仪的方法,该方法可在±1%-3%的精度范围内测量约1毫摩尔浓度。采取适当的预防措施后,所有化合物对质子具有相同的核磁共振“吸收系数”。对于分子量为5000的蛋白质和核酸,大约需要2毫克样品,不过使用较少量样品也能进行不太精确的测定。该技术使用标准化的内参试剂化合物,即二甲胂酸或3-(三甲基硅烷基)丙酸-2,2,3,3-d(4)酸钠盐。使用长脉冲间隔对光谱进行信号平均,以便相对于参考标准对不可交换质子的积分进行定量。准确的测定需要仔细优化磁场的均匀性,并精心注意样品制备和光谱处理。误差的主要来源通常是微量移液器的精度。如果能够消除样品制备误差,当前一代核磁共振光谱仪的精度下限可能接近0.4%。然而,这需要样品纯度>99.5%。文中描述了确定标准品浓度的方法,并以DNA单核苷酸和寡核苷酸为例进行了说明。类似的程序应该适用于蛋白质、多糖和其他生物分子,精度和精密度大致相同。

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