Literature DB >> 14673816

Enzymatic strategies for the characterization of nucleic acids by electrospray ionization mass spectrometry.

Allison P Null1, Linda M Benson, David C Muddiman.   

Abstract

Electrospray ionization mass spectrometry (ESI-MS) is a powerful technique used for the identification and characterization of DNA polymorphisms. Continual improvement in instrument design assures high mass measurement accuracy, sensitivity, and resolving power. This work describes an eclectic array of enzymatic strategies we have invoked in order to detect single-nucleotide polymorphisms by ESI-MS, although other applications may be envisioned. One strategy combines the use of two enzymes, exonuclease III and lambda exonuclease, to provide a ladder of single-stranded DNA fragments for straightforward sequence identification by mass spectrometry. A second strategy combines restriction enzymes to screen for polymorphisms present within specific amplicons. Finally, we describe the use of stable-isotope-labeled nucleotides for the determination of length and base composition of a PCR product. Copyright 2003 John Wiley & Sons, Ltd.

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Year:  2003        PMID: 14673816     DOI: 10.1002/rcm.1255

Source DB:  PubMed          Journal:  Rapid Commun Mass Spectrom        ISSN: 0951-4198            Impact factor:   2.419


  4 in total

1.  Some guidelines for the analysis of genomic DNA by PCR-LC-ESI-MS.

Authors:  Herbert Oberacher; Harald Niederstätter; Bruno Casetta; Walther Parson
Journal:  J Am Soc Mass Spectrom       Date:  2006-01-10       Impact factor: 3.109

2.  Sequence verification of oligonucleotides containing multiple arylamine modifications by enzymatic digestion and liquid chromatography mass spectrometry (LC/MS).

Authors:  Lan Gao; Li Zhang; Bongsup P Cho; M Paul Chiarelli
Journal:  J Am Soc Mass Spectrom       Date:  2008-05-10       Impact factor: 3.109

Review 3.  Reversed-phase separation methods for glycan analysis.

Authors:  Gerda C M Vreeker; Manfred Wuhrer
Journal:  Anal Bioanal Chem       Date:  2016-11-25       Impact factor: 4.142

4.  Improved Polymerase Chain Reaction-restriction Fragment Length Polymorphism Genotyping of Toxic Pufferfish by Liquid Chromatography/Mass Spectrometry.

Authors:  Hajime Miyaguchi
Journal:  J Vis Exp       Date:  2016-09-20       Impact factor: 1.355

  4 in total

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