Characterization of synthetic oligonucleotides containing biologically important modified bases by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry

被引:30
作者
Cui, Zhengfang [1 ]
Theruvathu, Jacob A. [1 ]
Farrel, Alvin [1 ]
Burdzy, Artur [1 ]
Sowers, Lawrence C. [1 ]
机构
[1] Loma Linda Univ, Sch Med, Dept Basic Sci, Loma Linda, CA 92350 USA
关键词
MALDI-TOF; base analogs; synthetic oligonucleotides; oxidative damage; isotope cluster;
D O I
10.1016/j.ab.2008.04.031
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Oligonucleotides containing modified bases are commonly used for biochemical and biophysical studies to assess the impact of specific types of chemical damage on DNA structure and function. In contrast to the synthesis of oligonucleotides with normal DNA bases, oligonucleotide synthesis with modified bases often requires modified synthetic or deprotection conditions. Furthermore, several modified bases of biological interest are prone to further damage during synthesis and oligonucleotide isolation. In this article, we describe the application of matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) to the characterization of a series of modified synthetic oligonucleotides. The potential for and limits in obtaining high mass accuracy for confirming oligonucleotide composition are discussed. Examination of the isotope cluster is also proposed as a method for confirming oligonucleotide elemental composition. MALDI-TOF-MS analysis of the unpurified reaction mixture can be used to confirm synthetic sequence and to reveal potential problems during synthesis. Analysis during and after purification can yield important information on depurination and base oxidation. It can also reveal unexpected problems that can occur with nonstandard synthesis, deprotection, or purification strategies. Proper characterization of modified oligonucleotides is essential for the correct interpretation of experiments performed with these substrates, and MALDI-TOF-MS analysis provides a simple yet extensive method of characterization that can be used at multiple stages of oligonucleotide production and use. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:196 / 207
页数:12
相关论文
共 62 条
  • [1] Thermodynamics and NMR of internal GT mismatches in DNA
    Allawi, HT
    SantaLucia, J
    [J]. BIOCHEMISTRY, 1997, 36 (34) : 10581 - 10594
  • [2] Bartolini WP, 2000, J MASS SPECTROM, V35, P408, DOI 10.1002/(SICI)1096-9888(200003)35:3<408::AID-JMS951>3.0.CO
  • [3] 2-0
  • [4] Synthesis and mass spectrometry analysis of oligonucleotides bearing 5-formyl-2'-deoxyuridine in their structure
    Berthod, T
    Petillot, Y
    Guy, A
    Cadet, J
    Forest, E
    Molko, D
    [J]. NUCLEOSIDES & NUCLEOTIDES, 1996, 15 (7-8): : 1287 - 1305
  • [5] 5-chloro-2′-deosyuridine cytotoxicity results from base excision repair of uracil subsequent to thymidylate synthase inhibition
    Brandon, ML
    Mi, LJ
    Chaung, WR
    Teebor, G
    Boorstein, RJ
    [J]. MUTATION RESEARCH-DNA REPAIR, 2000, 459 (02): : 161 - 169
  • [6] BROWNE DR, 1982, JOURNALISM QUART, V59, P663
  • [7] AN NMR STRUCTURAL STUDY OF DEAMINATED BASE-PAIRS IN DNA
    CARBONNAUX, C
    FAZAKERLEY, GV
    SOWERS, LC
    [J]. NUCLEIC ACIDS RESEARCH, 1990, 18 (14) : 4075 - 4081
  • [8] Synthesis and characterization of oligonucleotides containing a 4′-keto abasic site
    Chen, JY
    Stubbe, J
    [J]. BIOCHEMISTRY, 2004, 43 (18) : 5278 - 5286
  • [9] Recent highlights in modified oligonucleotide chemistry
    Cobb, Alexander J. A.
    [J]. ORGANIC & BIOMOLECULAR CHEMISTRY, 2007, 5 (20) : 3260 - 3275