Traceable phosphorus measurements by ICP-OES and HPLC for the quantitation of DNA

被引:45
作者
Holden, Marcia J. [1 ]
Rabb, Savelas A. [1 ]
Tewari, Yadu B. [1 ]
Winchester, Michael R. [1 ]
机构
[1] Natl Inst Stand & Technol, Chem Sci & Technol Lab, Gaithersburg, MD 20899 USA
关键词
D O I
10.1021/ac061463b
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Measurement of the phosphorus content of nucleotides and deoxyribonucleic acid (DNA) offers an approach to the quantitation of nucleic acids that is traceable to the SI. Such measurements can be an alternative to the commonly used spectroscopic tools that are not traceable. Phosphorus measurements of thymidine 5'-monophosphate (TMP) and acid-digested plasmid and genomic DNA preparations were made using high-performance inductively coupled plasma optical emission spectroscopy (HP-ICP-OES) and high-performance liquid chromatography (HPLC) and compared for bias and uncertainty. A prerequisite for quality measurement is the purity of the materials. Quantitation with the two platforms was comparable for the TMP. However, the HPLC values had larger uncertainties and were all statistically different from the gravimetric values at the 95% confidence level. When using ICP-OES, the digestion of the nucleotide monophosphate can be eliminated, thus simplifying the procedure. The differences between the results obtained by using the two platforms, when measuring genomic or plasmid DNA, were dependent on the mass fraction of the digest. ICP-OES measurement of phosphorus provides a highly accurate quantitation for both nucleotide monophosphates and DNA with expanded uncertainties of less than 0.1%. Currently, ICP-OES requires a significant sample size restricting its usefulness for the quantitation of DNA but represents a valuable tool for certification of reference materials. HPLC requires smaller amounts of material to perform the analysis but is less useful for certification of reference materials because of lower accuracy and 10-fold higher expanded uncertainties.
引用
收藏
页码:1536 / 1541
页数:6
相关论文
共 34 条
[1]  
BEAVEN GH, 1955, NUCL ACIDS CHEM BIOL, V1
[2]   Structural identification and quantification of protein phosphorylations after gel electrophoretic separation using Fourier transform ion cyclotron resonance mass spectrometry and laser ablation inductively coupled plasma mass spectrometry [J].
Becker, JS ;
Boulyga, SF ;
Becker, JS ;
Pickhardt, C ;
Damoc, E ;
Przybylski, M .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2003, 228 (2-3) :985-997
[3]   Determination of phosphorus and metals in human brain proteins after isolation by gel electrophoresis by laser ablation inductively coupled plasma source mass spectrometry [J].
Becker, JS ;
Zoriy, M ;
Becker, JS ;
Pickhardt, C ;
Przybylski, M .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 2004, 19 (01) :149-152
[4]   Thermodynamics of reactions catalyzed by anthranilate synthase [J].
Byrnes, WM ;
Goldberg, RN ;
Holden, MJ ;
Mayhew, MP ;
Tewari, YB .
BIOPHYSICAL CHEMISTRY, 2000, 84 (01) :45-64
[5]  
CHARGAFF E, 1948, J BIOL CHEM, V173, P327
[6]   Detection of metals in proteins by means of polyacrylamide gel electrophoresis and laser ablation-inductively coupled plasma-mass spectrometry:: Application to selenium [J].
Chéry, CC ;
Günther, D ;
Cornelis, R ;
Vanhaecke, F ;
Moens, L .
ELECTROPHORESIS, 2003, 24 (19-20) :3305-3313
[7]  
DeBievre P, 1997, METROLOGIA, V34, P67, DOI 10.1088/0026-1394/34/1/10
[8]   A comparison of enzymatic digestion for the quantitation of an oligonucleotide by liquid chromatography-isotope dilution mass spectrometry [J].
Donald, CE ;
Stokes, P ;
O'Connor, G ;
Woolford, AJ .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2005, 817 (02) :173-182
[9]   Quantitative determination of melphalan DNA adducts using HPLC - inductively coupled mass spectrometry [J].
Edler, M ;
Jakubowski, N ;
Linscheid, M .
JOURNAL OF MASS SPECTROMETRY, 2006, 41 (04) :507-516
[10]   Styrene oxide DNA adducts:: quantitative determination using 31P monitoring [J].
Edler, M ;
Jakubowski, N ;
Linscheid, M .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2005, 381 (01) :205-211