4.8 Article

Hybrid Activation Methods for Elucidating Nucleic Acid Modifications

期刊

ANALYTICAL CHEMISTRY
卷 83, 期 1, 页码 303-310

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ac102411a

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资金

  1. Robert A. Welch Foundation [F-1155]
  2. National Institutes of Health [RO1 GM65956]
  3. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM065956] Funding Source: NIH RePORTER

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Hybrid tandem mass spectrometry (MS/MS) techniques combining electron transfer (ET) and collision activated dissociation (CAD), infrared multiphoton dissociation (IRMPD), or ultraviolet photodissociation (UVPD) were implemented and evaluated for the characterization of a series of oligonucleotides and oligoribonucleotides, including both native single strands and single strands containing platinated, phosphorothioated, and 2'-O-methylated modification sites. ET-IRMPD and ET-UVPD of oligodeoxynucleotides and oligoribonucleotides resulted in rich fragmentation with respect to production of w, a, z, and d ions for DNA, and c, y, w, a-B, d, and z ions for RNA, with many product ions retaining the modification and thus allowing site specific identification. ET-IRMPD caused more extensive secondary dissociation of the ions, in addition to a broader distribution of detectable sequence ions attributed to using a lower mass cutoff. ET-UVPD promoted higher energy fragmentation pathways and created the most diverse MS/MS spectra. The numerous products generated by the hybrid MS/MS techniques resulted in specific and extensive backbone cleavages which allowed the modification sites of multiply modified oligonucleotides to be elucidated.

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