Evidence map›Paper›PMID 33184759›Full record

ArticleAnalytical and bioanalytical chemistry2021

Quantitative detection of ricin in beverages using trypsin/Glu-C tandem digestion coupled with ultra-high-pressure liquid chromatography-tandem mass spectrometry.

Long-Hui Liang, Xi Cheng, Hui-Lan Yu, Yang Yang, Xi-Hui Mu, Bo Chen, Xiao-Sen Li, Ji-Na Wu, Long Yan, Chang-Cai Liu and 1 more

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Article in Analytical and bioanalytical chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 34% of its field
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 2 countries.

Long-Hui LiangState Key Laboratory of NBC Protection for Civilian, Beijing, 102205, China.
Xi ChengThe Laboratory of Analytical Chemistry, Research Institute of Chemical Defence, Beijing, 102205, China.
Hui-Lan YuState Key Laboratory of NBC Protection for Civilian, Beijing, 102205, China.
Yang YangState Key Laboratory of NBC Protection for Civilian, Beijing, 102205, China.
Xi-Hui MuState Key Laboratory of NBC Protection for Civilian, Beijing, 102205, China.
Bo ChenThe Laboratory of Analytical Chemistry, Research Institute of Chemical Defence, Beijing, 102205, China.
Xiao-Sen LiState Key Laboratory of NBC Protection for Civilian, Beijing, 102205, China.
Ji-Na WuThe Laboratory of Analytical Chemistry, Research Institute of Chemical Defence, Beijing, 102205, China.
Long YanState Key Laboratory of NBC Protection for Civilian, Beijing, 102205, China.
Chang-Cai LiuState Key Laboratory of NBC Protection for Civilian, Beijing, 102205, China. liuchangcai@sklnbcpc.cn.
Shi-Lei LiuState Key Laboratory of NBC Protection for Civilian, Beijing, 102205, China. liu_shilei@lacricd.com.
China National Petroleum Corporation (China) · CNInstitute of Plant Protection · CN

Funding

State Key Laboratory of NBC Protection for Civilian SKLNBC2018-10
6 · The paper itself

Abstract

The toxic protein of ricin has drawn wide attention in recent years as a potential bioterrorism agent due to its high toxicity and wide availability. For the verification of the potential anti-terrorism activities, it is urgent for the quantification of ricin in food-related matrices. Here, a novel strategy of trypsin/Glu-C tandem digestion was introduced for quantitative detection of ricin marker peptides in several beverage matrices using isotope-labeled internal standard (IS)-mass spectrometry. The ricin in beverages was captured and enriched by biotinylated anti-ricin polyclonal antibodies conjugated to streptavidin magnetic beads. The purified ricin was cleaved using the developed trypsin/Glu-C tandem digestion method and then quantitatively detected by ultra-high-pressure liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) with isotope-labeled T7A and TG11B selected as IS. The use of trypsin/Glu-C digestion allows shorter peptides, which are more suitable for MS detection, to be obtained than the use of single trypsin digestion. Under the optimized tandem digestion condition, except for T7A in the A-chain, two resulting specific peptides of TG13A, TG28A from the A-chain and two of TG11B, TG33B from the B-chain were chosen as novel marker peptides with high MS response. The uniqueness of the selected marker peptides allows for unambiguous identification of ricin among its homologous proteins in a single run. The MS response of the four novel marker peptides is increased by more than 10 times compared with that of individual corresponding tryptic peptides. Both the marker peptides of A-chain T7A and B-chain TG11B were selected as quantitative peptides based on the highest MS response among the marker peptides from their individual chains. The limit of detection (LOD) of ricin is 0.1 ng/mL in PBS and 0.5 ng/mL in either milk or orange juice. The linear range of calibration curves for ricin were 0.5-300 ng/mL in PBS, 1.0-400 ng/mL in milk, and 1.0-250 ng/mL in orange juice. The method accuracy ranged between 82.6 and 101.8% for PBS, 88.9-105.2% for milk, and 95.3-118.7% for orange juice. The intra-day and inter-day precision had relative standard deviations (%RSD) of 0.3-9.4%, 0.7-8.9%, and 0.2-6.9% in the three matrices respectively. Furthermore, whether T7A or TG11B is used as a quantitative peptide, the quantitative results of ricin are consistent. This study provides not only a practical method for the absolute quantification of ricin in beverage matrices but also a new strategy for the investigation of illegal use of ricin in chemical weapon verification tasks such as OPCW biotoxin sample analysis exercises.

Indexed as

BeveragesBiotinylationCalibrationChromatography, High Pressure LiquidIsotope LabelingLimit of DetectionMagneticsPeptidesQuality ControlReproducibility of ResultsRicinSensitivity and SpecificitySolventsStreptavidinTandem Mass SpectrometryTrypsinPeptidesRicinSolventsStreptavidinTrypsinImmunocaptureMarker peptidesRicinTandem digestionUHPLC-ESI-MS/MS

Identifiers

PMID33184759
OpenAlexW3103067164

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.