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Water cluster calibration reduces mass error in electrospray ionization mass spectrometry of proteins

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Journal of the American Society for Mass Spectrometry

Abstract

Herein we report a novel calibration routine for use in positive ion mode electrospray ionization mass spectrometry (ESI-MS). Monoisotopic masses were calculated for a series of water clusters and used as calibration reference files (available at http://www.hbcg.utmb.edu/xray). The water cluster series contains singly charged peaks every 18 Da, which allows calibration curves to be precisely defined over a broad mass-to-charge ratio range. Water clusters, induced by a combination of high flow rate and high cone voltage, were used to accurately calibrate a quadrupole mass spectrometer from 100 to 1900 m/z. Calibration curves thus generated have many more data points and greatly reduced standard deviations compared to those obtained from myoglobin, sodium iodide, cesium iodide, or poly(ethylene glycol) based calibration standards. This calibration routine reduces the error in protein mass measurements by a factor of 3, from ±0.01% to ±0.0035% at the 95% confidence limit. The implications of this increased mass accuracy and wider calibrated mass-to-charge ratio scale for the study of protein sequence, structure, and folding by ESI-MS are discussed.

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Authors and Affiliations

  1. The Department of Human Biological Chemistry and Genetics and The Sealy Center for Structural Biology, University of Texas Medical Branch, Galveston, Texas, USA

    David W. Ledman & Robert O. Fox

  2. The Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut, USA

    David W. Ledman

Authors
  1. David W. Ledman
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  2. Robert O. Fox
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Correspondence to Robert O. Fox.

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Ledman, D.W., Fox, R.O. Water cluster calibration reduces mass error in electrospray ionization mass spectrometry of proteins. J Am Soc Mass Spectrom 8, 1158–1164 (1997). https://doi.org/10.1016/S1044-0305(97)00157-8

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  • DOI: https://doi.org/10.1016/S1044-0305(97)00157-8

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