Literature DB >> 2952191

Characterization of an alkylated dinucleotide by desorption chemical ionization and tandem mass spectrometry.

I Isern-Flecha, X Y Jiang, R G Cooks, W Pfleiderer, W G Chae, C J Chang.   

Abstract

A highly sensitive (subpicomole level), structure-specific method of analysis has been developed for characterizing and quantitating the dinucleotide thymidylyl(3'----5')thymidine methyl phosphotriester by desorption chemical ionization tandem mass spectrometry. The methodology can be applied to related compounds such as the parent dinucleotide and employs either positive or negative ionization mass spectra or daughter spectra. The procedure allows specification of the site of methyl attachment.

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Year:  1987        PMID: 2952191     DOI: 10.1002/bms.1200140106

Source DB:  PubMed          Journal:  Biomed Environ Mass Spectrom        ISSN: 0887-6134


  3 in total

1.  Methyl guanine isomer distinction by hydrogen / deuterium exchange using a fourier transform mass spectrometer.

Authors:  B D Nourse; R L Hettich; M V Buchanan
Journal:  J Am Soc Mass Spectrom       Date:  1993-04       Impact factor: 3.109

2.  Structural Characterization of Normal and Modified Oligonucleotides by Matrix-assisted Laser Desorption Fourier Transform Mass Spectrometry.

Authors:  R Hettich; M Buchanan
Journal:  J Am Soc Mass Spectrom       Date:  1991-09       Impact factor: 3.109

3.  Tandem mass spectrometry of small, multiply charged oligonucleotides.

Authors:  S A McLuckey; G J Van Berkel; G L Glish
Journal:  J Am Soc Mass Spectrom       Date:  1992-01       Impact factor: 3.109

  3 in total

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