Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry protocol for monitoring the progress of enzymatic 13C/15N-labeled DNA syntheses

被引:3
作者
Ambrus, A [1 ]
Chen, D
Whatcott, C
Somogyi, A
Yang, DZ
机构
[1] Univ Arizona, Dept Pharmacol & Toxicol, Tucson, AZ 85721 USA
[2] Univ Arizona, Dept Chem, Tucson, AZ 85721 USA
[3] Univ Arizona, Arizona Canc Ctr, Tucson, AZ 85724 USA
关键词
labeling; monitoring; progress; DNA; NMR; mass spectrometry; synthesis;
D O I
10.1016/j.ab.2005.04.008
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
We demonstrate that a simple matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry protocol provides a rapid and accurate method for monitoring the stage and completeness of enzymatic DNA syntheses. A crucial step of these syntheses is to quench the reaction at the desired nucleotide length. This is especially important when expensive, e.g., C-13/N-15-labeled DNA segments, are synthesized for multinuclear magnetic resonance purposes to reveal detailed structural information. The analyses of three templates for a human telomeric 22-mer, a wild type, and a mutant human c-MYC promoter (18- and 22-mer) DNA and their reactions with the 3'-5' exo(-) Klenow fragment of DNA polymerase I demonstrate the usefulness of our protocol. Small amounts of samples (ca. 1-2 mu l each) were taken from the reaction mixtures at different times and analyzed promptly by MALDI-TOF, applying our successive on-plate desalting method that eliminates the insensitivity of the MALDI technique at high salt content. The progress of the reaction was detected by monitoring the relative intensity ratios of ions corresponding to the desired products and the primer-template complexes. The effectiveness of NH3 cleavage leading to final products was also followed by MALDI-TOF in Successful enzymatic reactions. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:246 / 253
页数:8
相关论文
共 11 条
[1]
Solution structure of the biologically relevant g-quadruplex element in the human c-MYC promoter. implications for g-quadruplex stabilization [J].
Ambrus, A ;
Chen, D ;
Dai, JX ;
Jones, RA ;
Yang, DZ .
BIOCHEMISTRY, 2005, 44 (06) :2048-2058
[2]
Chen ZD, 1996, BIOTECHNIQUES, V21, P820
[3]
NOVEL BLUNT-END ADDITION-REACTIONS CATALYZED BY DNA-POLYMERASE-I OF ESCHERICHIA-COLI [J].
CLARK, JM ;
JOYCE, CM ;
BEARDSLEY, GP .
JOURNAL OF MOLECULAR BIOLOGY, 1987, 198 (01) :123-127
[4]
A dimeric DNA interface stabilized by stacked A•(G•G•G•G)•A hexads and coordinated monovalent cations [J].
Kettani, A ;
Gorin, A ;
Majumdar, A ;
Hermann, T ;
Skripkin, E ;
Zhao, H ;
Jones, R ;
Patel, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 297 (03) :627-644
[5]
Interlocked mismatch-aligned arrowhead DNA motifs [J].
Kettani, A ;
Bouaziz, S ;
Skripkin, E ;
Majumdar, A ;
Wang, WM ;
Jones, RA ;
Patel, DJ .
STRUCTURE, 1999, 7 (07) :803-815
[6]
DNA sequence analysis by MALDI mass spectrometry [J].
Kirpekar, F ;
Nordhoff, E ;
Larsen, LK ;
Kristiansen, K ;
Roepstorff, P ;
Hillenkamp, F .
NUCLEIC ACIDS RESEARCH, 1998, 26 (11) :2554-2559
[7]
Simple, efficient protocol for enzymatic synthesis of uniformly 13C,15N-labeled DNA for heteronuclear NMR studies [J].
Masse, JE ;
Bortmann, P ;
Dieckmann, T ;
Feigon, J .
NUCLEIC ACIDS RESEARCH, 1998, 26 (11) :2618-2624
[8]
A site-specific low-enrichment 15N,13C isotope-labeling approach to unambiguous NMR spectral assignments in nucleic acids [J].
Phan, AT ;
Patel, DJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (07) :1160-1161
[9]
Efficient enzymatic synthesis of C-13,N-15-labeled DNA for NMR studies [J].
Smith, DE ;
Su, JY ;
Jucker, FM .
JOURNAL OF BIOMOLECULAR NMR, 1997, 10 (03) :245-253
[10]
SOLUTION STRUCTURE OF THE HUMAN TELOMERIC REPEAT D[AG(3)(T(2)AG(3))3] G-TETRAPLEX [J].
WANG, Y ;
PATEL, DJ .
STRUCTURE, 1993, 1 (04) :263-282