Use of elemental analysis to determine comparative performance of established DNA quantification methods

被引:33
作者
English, Claire A. [1 ]
Merson, Sheila [1 ]
Keer, Jacquie T. [1 ]
机构
[1] Lab Govt Chemist, Biomol Innovat, Teddington TW11 0LY, Middx, England
关键词
D O I
10.1021/ac060174k
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Quantification of genomic DNA is critical for many analyses in molecular biology. Current methods include optical density ( OD) measurements or fluorescent enhancement but both approaches have limitations on achievable accuracy. In this study we performed an elemental analysis to quantify genomic DNA to provide an independent value for comparing the performance of four quantification methods. Specifically ICP-OES ( inductively coupled plasma-optical emission spectroscopy) was used to assign a concentration value to a DNA stock solution, based on the stoichiometry of phosphorus within the molecule. Two absorbance- and two fluorescence-based methods were then used to quantify the same DNA solution using replicate analyses. The precision of each method was assessed by measurement of replicate spread ( coefficient of variation) and trueness by t-test. Results showed that performance of the methods was variable, both in terms of concordance with the independent ICP-OES value and repeatability of data. While need for expensive equipment and technical expertise may preclude widespread replacement of more traditional methods for DNA quantification, use of primary methods such as ICP-OES analysis for production of accurate calibrants may increase quantitative accuracy and give greater appreciation of the true performance of current methods.
引用
收藏
页码:4630 / 4633
页数:4
相关论文
共 13 条
[1]   PicoGreen quantitation of DNA: Effective evaluation of samples pre- or post-PCR [J].
Ahn, SJ ;
Costa, J ;
Emanuel, JR .
NUCLEIC ACIDS RESEARCH, 1996, 24 (13) :2623-2625
[2]   Revised UV extinction coefficients for nucleoside-5'-monophosphates and unpaired DNA and RNA [J].
Cavaluzzi, MJ ;
Borer, PN .
NUCLEIC ACIDS RESEARCH, 2004, 32 (01) :e13
[3]   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
[4]   NIST Mixed Stain Study 3: Signal intensity balance in commercial short tandem repeat multiplexes [J].
Duewer, DL ;
Kline, MC ;
Redman, JW ;
Butler, JM .
ANALYTICAL CHEMISTRY, 2004, 76 (23) :6928-6934
[5]   Quantitation of circulating DNA in the serum of breast cancer patients by real-time PCR [J].
Gal, S ;
Fidler, C ;
Lo, YMD ;
Taylor, M ;
Han, C ;
Moore, J ;
Harris, AL ;
Wainscoat, JS .
BRITISH JOURNAL OF CANCER, 2004, 90 (06) :1211-1215
[6]   Performance of high-throughput DNA quantification methods [J].
Haque, KA ;
Pfeiffer, RM ;
Beerman, MB ;
Struewing, JP ;
Chanock, SJ ;
Bergen, AW .
BMC BIOTECHNOLOGY, 2003, 3 (1)
[7]   NIST mixed stain study 3: DNA quantitation accuracy and its influence on short tandem repeat multiplex signal intensity [J].
Kline, MC ;
Duewer, DL ;
Redman, JW ;
Butler, JM .
ANALYTICAL CHEMISTRY, 2003, 75 (10) :2463-2469
[8]   Initial sequencing and analysis of the human genome [J].
Lander, ES ;
Int Human Genome Sequencing Consortium ;
Linton, LM ;
Birren, B ;
Nusbaum, C ;
Zody, MC ;
Baldwin, J ;
Devon, K ;
Dewar, K ;
Doyle, M ;
FitzHugh, W ;
Funke, R ;
Gage, D ;
Harris, K ;
Heaford, A ;
Howland, J ;
Kann, L ;
Lehoczky, J ;
LeVine, R ;
McEwan, P ;
McKernan, K ;
Meldrim, J ;
Mesirov, JP ;
Miranda, C ;
Morris, W ;
Naylor, J ;
Raymond, C ;
Rosetti, M ;
Santos, R ;
Sheridan, A ;
Sougnez, C ;
Stange-Thomann, N ;
Stojanovic, N ;
Subramanian, A ;
Wyman, D ;
Rogers, J ;
Sulston, J ;
Ainscough, R ;
Beck, S ;
Bentley, D ;
Burton, J ;
Clee, C ;
Carter, N ;
Coulson, A ;
Deadman, R ;
Deloukas, P ;
Dunham, A ;
Dunham, I ;
Durbin, R ;
French, L .
NATURE, 2001, 409 (6822) :860-921
[9]   Concentration and extinction coefficient determination for oligonucleotides and analogs using a general phosphate analysis [J].
Murphy, JH ;
Trapane, TL .
ANALYTICAL BIOCHEMISTRY, 1996, 240 (02) :273-282
[10]  
Rengarajan K, 2002, MOL VIS, V8, P416