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Determination of denaturated proteins and biotoxins by on-line size-exclusion chromatography-digestion-liquid chromatography-electrospray mass spectrometry

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Author: Carol, J. · Gorseling, M.C.J.K. · Jong, C.F. de · Lingeman, H. · Kientz, C.E. · Baar, B.L.M. van · Irth, H.
Type:article
Date:2005
Institution: TNO Defensie en Veiligheid
Source:Analytical Biochemistry, 1, 346, 150-157
Identifier: 238786
doi: doi:10.1016/j.ab.2005.08.023
Keywords: Biological toxins · Liquid chromatography · Mass spectrometry · On-line digestion · Size-exclusion chromatography · Bovine serum albumin · Cholera toxin · Myoglobin · Staphylococcus enterotoxin · Article · Desalination · Digestion · Electrospray mass spectrometry · Gel permeation chromatography · Nonhuman · Priority journal · Protein analysis · Protein determination · Reversed phase high performance liquid chromatography · Amino Acid Sequence · Cholera Toxin · Chromatography, Gel · Chromatography, Liquid · Enterotoxins · Molecular Sequence Data · Protein Denaturation · Proteins · Spectrometry, Mass, Electrospray Ionization · Bovinae · Chemicals / CAS: Cholera Toxin, 9012-63-9; enterotoxin B, staphylococcal, 39424-53-8; Enterotoxins; Proteins

Abstract

A multidimensional analytical method for the rapid determination and identification of proteins has been developed. The method is based on the size-exclusion fractionation of protein-containing samples, subsequent on-line trypsin digestion and desalination, and reversed-phase high-performance liquid chromatography-electrospray mass spectrometry detection. The present system reduces digestion times to 20 min and the total analysis time to less than 100 min. Using bovine serum albumin and myoglobin as model proteins, optimization of key parameters such as digestion times and interfacing conditions between the different pretreatment steps was performed. The automated system was tested for the identification of infectious disease agents such as cholera toxin and staphylococcal enterotoxin B. This resulted typically in a positive identification by a total sequence coverage of approximately 40%. © 2005 Elsevier Inc. All rights reserved.