Cavaluzzi Michael J, Borer Philip N
Department of Chemistry and Graduate Program in Structural Biology, Biochemistry and Biophysics, Syracuse University, NY 13244-4100, USA.
Nucleic Acids Res. 2004 Jan 13;32(1):e13. doi: 10.1093/nar/gnh015.
Ultraviolet absorption provides the nearly universal basis for determining concentrations of nucleic acids. Values for the UV extinction coefficients of DNA and RNA rely on the mononucleotide values determined 30-50 years ago. We show that nearly all of the previously published extinction coefficients for the nucleoside-5'-monophosphates are too large, and in error by as much as 7%. Concentrations based on complete hydrolysis and the older set of values are too low by approximately 4% for typical RNA and 2-3% for typical DNA samples. We also analyzed data in the literature for the extinction coefficients of unpaired DNA oligomers. Robust prediction of concentrations can be made using 38 microg/A260 unit for single-stranded DNA (ssDNA) having non-repetitive sequences and 40-80% GC. This is superior to currently used predictions that account for nearest-neighbor frequency or base composition. The latter result in concentrations that are 10-30% too low for typical ssDNA used as primers for PCR and other similar techniques. Methods are described here to accurately measure concentrations of nucleotides by nuclear magnetic resonance. NMR can be used to accurately determine concentrations (and extinction coefficients) of biomolecules within 1%.
紫外吸收为测定核酸浓度提供了几乎通用的基础。DNA和RNA的紫外消光系数值依赖于30到50年前测定的单核苷酸值。我们发现,几乎所有先前发表的核苷 - 5'-单磷酸的消光系数都过大,误差高达7%。基于完全水解和旧值集计算出的典型RNA浓度约低4%,典型DNA样本浓度约低2 - 3%。我们还分析了文献中关于未配对DNA寡聚物消光系数的数据。对于具有非重复序列且GC含量为40 - 80%的单链DNA(ssDNA),使用38μg/A260单位可对浓度进行可靠预测。这优于目前使用的考虑最近邻频率或碱基组成的预测方法。对于用作PCR和其他类似技术引物的典型ssDNA,后者得出的浓度低10 - 30%。本文描述了通过核磁共振准确测量核苷酸浓度的方法。核磁共振可用于在1%的误差范围内准确测定生物分子的浓度(和消光系数)。