Literature DB >> 9253245

Quantification of biomolecules by external electrospray ionization Fourier transform mass spectrometry.

H R Padley1, S Bashir, T D Wood.   

Abstract

Fourier transform mass spectrometry (FTMS) is well-known for its capabilities in structural characterization of molecules. Recent developments in radio frequency excitation, linearized trapping, and accumulation of ions generated from external sources have improved the potential of FTMS for quantitative analysis. Here, a commercial external electrospray ionization FTMS, employing a linearized ion trap (the Infinity Cell) and an ion accumulation procedure in which ions are deflected off-axis and injected into the trap, is evaluated as an analytical method for quantifying amino acids, peptides, and proteins. Linear response over approximately 2-3 orders of magnitude is observed for singly-charged ions with low coefficients of variation (generally < 10%), and the calibration curves generated can be used to quantify structurally similar analytes with < 4% relative error, as shown here for quantification of leucine enkephalin from curves generated by methionine enkephalin. Similar precision is obtained for multiply-charged lysozyme, but over only 1.5 orders of magnitude. Some m/z discrimination is observed as a function of trap accumulation potential for a two-component cytochrome c/lysozyme mixture. The results are promising because they suggest that quantification using liquid chromatography coupled to electrospray FTMS is possible.

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Year:  1997        PMID: 9253245     DOI: 10.1021/ac9700235

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  4 in total

1.  Suppression correction and characteristic study in liquid chromatography/Fourier transform mass spectrometry measurements.

Authors:  Xuepo Ma; Travis J Hestilow; Jian Cui; Jianqiu Zhang
Journal:  Rapid Commun Mass Spectrom       Date:  2011-02-28       Impact factor: 2.419

2.  Using solution phase hydrogen/deuterium (H/D) exchange to determine the origin of non-covalent complexes observed by electrospray ionization mass spectrometry: in solution or in vacuo?

Authors:  S A Lorenz; E P Maziarz; T D Wood
Journal:  J Am Soc Mass Spectrom       Date:  2001-07       Impact factor: 3.262

3.  Processing methods for signal suppression of FTMS data.

Authors:  Xuepo Ma; Jian Cui; Jianqiu Zhang
Journal:  Proteome Sci       Date:  2011-10-14       Impact factor: 2.480

4.  The effect of adenine protonation on RNA phosphodiester backbone bond cleavage elucidated by deaza-nucleobase modifications and mass spectrometry.

Authors:  Elisabeth Fuchs; Christoph Falschlunger; Ronald Micura; Kathrin Breuker
Journal:  Nucleic Acids Res       Date:  2019-08-22       Impact factor: 16.971

  4 in total

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