Detection and Quantification of Ricin in Beverages Using Isotope Dilution Tandem Mass Spectrometry

The toxic plant protein ricin has gained notoriety due to wide availability and potential use as a bioterrorism agent, with particular concern for food supply contamination. We have developed a sensitive and selective mass spectrometry-based method to detect ricin in tap water, 2% milk, apple juice,...

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Published inAnalytical chemistry (Washington) Vol. 83; no. 8; pp. 2897 - 2905
Main Authors McGrath, Sara C, Schieltz, David M, McWilliams, Lisa G, Pirkle, James L, Barr, John R
Format Journal Article
LanguageEnglish
Published Washington, DC American Chemical Society 15.04.2011
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Abstract The toxic plant protein ricin has gained notoriety due to wide availability and potential use as a bioterrorism agent, with particular concern for food supply contamination. We have developed a sensitive and selective mass spectrometry-based method to detect ricin in tap water, 2% milk, apple juice, and orange juice. Ricin added to beverage matrices was extracted using antibody-bound magnetic beads and digested with trypsin. Absolute quantification was performed using isotope dilution mass spectrometry with a linear ion trap operating in product-ion-monitoring mode. The method allows for identification of ricin A chain and B chain and for distinction of ricin from ricin agglutinin within a single analytical run. Ricin-bound beads were also tested for deadenylase activity by incubation with a synthetic ssDNA oligomer. Depurination of the substrate by ricin was confirmed by matrix-assisted laser desorption ionization-time-of-flight mass spectrometry (MALDI-TOFMS). This method was used successfully to extract ricin from each beverage matrix. The activity of recovered ricin was assessed, and quantification was achieved, with a limit of detection of 10 fmol/mL (0.64 ng/mL).
AbstractList The toxic plant protein ricin has gained notoriety due to wide availability and potential use as a bioterrorism agent, with particular concern for food supply contamination. We have developed a sensitive and selective mass spectrometry-based method to detect ricin in tap water, 2% milk, apple juice, and orange juice. Ricin added to beverage matrices was extracted using antibody-bound magnetic beads and digested with trypsin. Absolute quantification was performed using isotope dilution mass spectrometry with a linear ion trap operating in product-ion-monitoring mode. The method allows for identification of ricin A chain and B chain and for distinction of ricin from ricin agglutinin within a single analytical run. Ricin-bound beads were also tested for deadenylase activity by incubation with a synthetic ssDNA oligomer. Depurination of the substrate by ricin was confirmed by matrix-assisted laser desorption ionization-time-of-flight mass spectrometry (MALDI-TOFMS). This method was used successfully to extract ricin from each beverage matrix. The activity of recovered ricin was assessed, and quantification was achieved, with a limit of detection of 10 fmol/mL (0.64 ng/mL).
The toxic plant protein ricin has gained notoriety due to wide availability and potential use as a bioterrorism agent, with particular concern for food supply contamination. We have developed a sensitive and selective mass spectrometry-based method to detect ricin in tap water, 2% milk, apple juice, and orange juice. Ricin added to beverage matrices was extracted using antibody-bound magnetic beads and digested with trypsin. Absolute quantification was performed using isotope dilution mass spectrometry with a linear ion trap operating in product-ion-monitoring mode. The method allows for identification of ricin A chain and B chain and for distinction of ricin from ricin agglutinin within a single analytical run. Ricin-bound beads were also tested for deadenylase activity by incubation with a synthetic ssDNA oligomer. Depurination of the substrate by ricin was confirmed by matrix-assisted laser desorption ionization-time-of-flight mass spectrometry (MALDI-TOFMS). This method was used successfully to extract ricin from each beverage matrix. The activity of recovered ricin was assessed, and quantification was achieved, with a limit of detection of 10 fmol/mL (0.64 ng/mL). [PUBLICATION ABSTRACT]
Author Barr, John R
McGrath, Sara C
Pirkle, James L
Schieltz, David M
McWilliams, Lisa G
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Issue 8
Keywords Identification
Matrix assisted laser desorption ionization
Oligomer
Ion trap
Plant
Sample preparation
Castor (seed)
Detection limit
Beverage
Monitoring
Quantitative analysis
Milk
Vegetals
Antibody
Isotope dilution
Foodstuff
Tap water
Contamination
Protein
Substrate
Apple
Time of flight method
Mass spectrometry MS/MS
Simultaneous measurement
Mass spectrometry
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2011 American Chemical Society
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Snippet The toxic plant protein ricin has gained notoriety due to wide availability and potential use as a bioterrorism agent, with particular concern for food supply...
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SubjectTerms Analytical chemistry
Beverages
Beverages - analysis
Chemistry
Exact sciences and technology
Food contamination & poisoning
Humans
Isotope Labeling - methods
Isotopes
Mass spectrometry
Proteins
Ricin - analysis
Spectrometric and optical methods
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Title Detection and Quantification of Ricin in Beverages Using Isotope Dilution Tandem Mass Spectrometry
URI http://dx.doi.org/10.1021/ac102571f
https://www.ncbi.nlm.nih.gov/pubmed/21428278
https://www.proquest.com/docview/865752690
Volume 83
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