Cargando…
Quantification of ricin, RCA and comparison of enzymatic activity in 18 Ricinus communis cultivars by isotope dilution mass spectrometry
The seeds of the Ricinus communis (Castor bean) plant are the source of the economically important commodity castor oil. Castor seeds also contain the proteins ricin and R. communis agglutinin (RCA), two toxic lectins that are hazardous to human health. Radial immunodiffusion (RID) and the enzyme li...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5303535/ https://www.ncbi.nlm.nih.gov/pubmed/25576235 http://dx.doi.org/10.1016/j.toxicon.2015.01.003 |
_version_ | 1782506730574315520 |
---|---|
author | Schieltz, David M. McWilliams, Lisa G. Kuklenyik, Zsuzsanna Prezioso, Samantha M. Carter, Andrew J. Williamson, Yulanda M. McGrath, Sara C. Morse, Stephen A. Barr, John R. |
author_facet | Schieltz, David M. McWilliams, Lisa G. Kuklenyik, Zsuzsanna Prezioso, Samantha M. Carter, Andrew J. Williamson, Yulanda M. McGrath, Sara C. Morse, Stephen A. Barr, John R. |
author_sort | Schieltz, David M. |
collection | PubMed |
description | The seeds of the Ricinus communis (Castor bean) plant are the source of the economically important commodity castor oil. Castor seeds also contain the proteins ricin and R. communis agglutinin (RCA), two toxic lectins that are hazardous to human health. Radial immunodiffusion (RID) and the enzyme linked immunosorbent assay (ELISA) are two antibody-based methods commonly used to quantify ricin and RCA; however, antibodies currently used in these methods cannot distinguish between ricin and RCA due to the high sequence homology of the respective proteins. In this study, a technique combining antibody-based affinity capture with liquid chromatography and multiple reaction monitoring (MRM) mass spectrometry (MS) was used to quantify the amounts of ricin and RCA independently in extracts prepared from the seeds of eighteen representative cultivars of R. communis which were propagated under identical conditions. Additionally, liquid chromatography and MRM-MS was used to determine rRNA N-glycosidase activity for each cultivar and the overall activity in these cultivars was compared to a purified ricin standard. Of the cultivars studied, the average ricin content was 9.3 mg/g seed, the average RCA content was 9.9 mg/g seed, and the enzymatic activity agreed with the activity of a purified ricin reference within 35% relative activity. |
format | Online Article Text |
id | pubmed-5303535 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
record_format | MEDLINE/PubMed |
spelling | pubmed-53035352017-02-11 Quantification of ricin, RCA and comparison of enzymatic activity in 18 Ricinus communis cultivars by isotope dilution mass spectrometry Schieltz, David M. McWilliams, Lisa G. Kuklenyik, Zsuzsanna Prezioso, Samantha M. Carter, Andrew J. Williamson, Yulanda M. McGrath, Sara C. Morse, Stephen A. Barr, John R. Toxicon Article The seeds of the Ricinus communis (Castor bean) plant are the source of the economically important commodity castor oil. Castor seeds also contain the proteins ricin and R. communis agglutinin (RCA), two toxic lectins that are hazardous to human health. Radial immunodiffusion (RID) and the enzyme linked immunosorbent assay (ELISA) are two antibody-based methods commonly used to quantify ricin and RCA; however, antibodies currently used in these methods cannot distinguish between ricin and RCA due to the high sequence homology of the respective proteins. In this study, a technique combining antibody-based affinity capture with liquid chromatography and multiple reaction monitoring (MRM) mass spectrometry (MS) was used to quantify the amounts of ricin and RCA independently in extracts prepared from the seeds of eighteen representative cultivars of R. communis which were propagated under identical conditions. Additionally, liquid chromatography and MRM-MS was used to determine rRNA N-glycosidase activity for each cultivar and the overall activity in these cultivars was compared to a purified ricin standard. Of the cultivars studied, the average ricin content was 9.3 mg/g seed, the average RCA content was 9.9 mg/g seed, and the enzymatic activity agreed with the activity of a purified ricin reference within 35% relative activity. 2015-01-07 2015-03 /pmc/articles/PMC5303535/ /pubmed/25576235 http://dx.doi.org/10.1016/j.toxicon.2015.01.003 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Schieltz, David M. McWilliams, Lisa G. Kuklenyik, Zsuzsanna Prezioso, Samantha M. Carter, Andrew J. Williamson, Yulanda M. McGrath, Sara C. Morse, Stephen A. Barr, John R. Quantification of ricin, RCA and comparison of enzymatic activity in 18 Ricinus communis cultivars by isotope dilution mass spectrometry |
title | Quantification of ricin, RCA and comparison of enzymatic activity in 18 Ricinus communis cultivars by isotope dilution mass spectrometry |
title_full | Quantification of ricin, RCA and comparison of enzymatic activity in 18 Ricinus communis cultivars by isotope dilution mass spectrometry |
title_fullStr | Quantification of ricin, RCA and comparison of enzymatic activity in 18 Ricinus communis cultivars by isotope dilution mass spectrometry |
title_full_unstemmed | Quantification of ricin, RCA and comparison of enzymatic activity in 18 Ricinus communis cultivars by isotope dilution mass spectrometry |
title_short | Quantification of ricin, RCA and comparison of enzymatic activity in 18 Ricinus communis cultivars by isotope dilution mass spectrometry |
title_sort | quantification of ricin, rca and comparison of enzymatic activity in 18 ricinus communis cultivars by isotope dilution mass spectrometry |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5303535/ https://www.ncbi.nlm.nih.gov/pubmed/25576235 http://dx.doi.org/10.1016/j.toxicon.2015.01.003 |
work_keys_str_mv | AT schieltzdavidm quantificationofricinrcaandcomparisonofenzymaticactivityin18ricinuscommuniscultivarsbyisotopedilutionmassspectrometry AT mcwilliamslisag quantificationofricinrcaandcomparisonofenzymaticactivityin18ricinuscommuniscultivarsbyisotopedilutionmassspectrometry AT kuklenyikzsuzsanna quantificationofricinrcaandcomparisonofenzymaticactivityin18ricinuscommuniscultivarsbyisotopedilutionmassspectrometry AT preziososamantham quantificationofricinrcaandcomparisonofenzymaticactivityin18ricinuscommuniscultivarsbyisotopedilutionmassspectrometry AT carterandrewj quantificationofricinrcaandcomparisonofenzymaticactivityin18ricinuscommuniscultivarsbyisotopedilutionmassspectrometry AT williamsonyulandam quantificationofricinrcaandcomparisonofenzymaticactivityin18ricinuscommuniscultivarsbyisotopedilutionmassspectrometry AT mcgrathsarac quantificationofricinrcaandcomparisonofenzymaticactivityin18ricinuscommuniscultivarsbyisotopedilutionmassspectrometry AT morsestephena quantificationofricinrcaandcomparisonofenzymaticactivityin18ricinuscommuniscultivarsbyisotopedilutionmassspectrometry AT barrjohnr quantificationofricinrcaandcomparisonofenzymaticactivityin18ricinuscommuniscultivarsbyisotopedilutionmassspectrometry |