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Absolute Quantification of Allergen Glb33 in Rice by Liquid Chromatography-Mass Spectrometry using Two Isotope-Labeled Standard Peptides.
Chen, Ming-Xue; Yang, Huan; Ma, You-Ning; Mou, Ren-Xiang; Zhu, Zhi-Wei; Cao, Zhao-Yun; Cheng, Fang-Min.
Afiliación
  • Chen MX; College of Agriculture and Biotechnology , Zhejiang University , Hangzhou 310058 , China.
  • Yang H; Rice Product Quality Inspection and Supervision Center, Ministry of Agriculture and Rural Affairs , China National Rice Research Institute , Hangzhou 310006 , China.
  • Ma YN; Rice Product Quality Inspection and Supervision Center, Ministry of Agriculture and Rural Affairs , China National Rice Research Institute , Hangzhou 310006 , China.
  • Mou RX; Rice Product Quality Inspection and Supervision Center, Ministry of Agriculture and Rural Affairs , China National Rice Research Institute , Hangzhou 310006 , China.
  • Zhu ZW; Rice Product Quality Inspection and Supervision Center, Ministry of Agriculture and Rural Affairs , China National Rice Research Institute , Hangzhou 310006 , China.
  • Cao ZY; Rice Product Quality Inspection and Supervision Center, Ministry of Agriculture and Rural Affairs , China National Rice Research Institute , Hangzhou 310006 , China.
  • Cheng FM; Rice Product Quality Inspection and Supervision Center, Ministry of Agriculture and Rural Affairs , China National Rice Research Institute , Hangzhou 310006 , China.
J Agric Food Chem ; 67(17): 5026-5032, 2019 May 01.
Article en En | MEDLINE | ID: mdl-30933518
Allergen Glb33 is an important allergen in rice that can cause allergic reactions such as asthma and atopic dermatitis. However, knowledge of the content in rice is sparse. In the present work, an absolute protein quantification method was established for allergen Glb33 in rice samples using liquid chromatography-tandem mass spectrometry. After extraction of allergen Glb33 from rice grains using salt solution, the isotope-labeled peptide internal standard was added to the extract, followed by enzymatic digestion with trypsin. The signature peptide and its isotope-labeled analogue from the tryptic hydrolysates of allergen Glb33 and the internal standard were detected by liquid chromatography-tandem mass spectrometry. The quantitative bias caused by tryptic efficiency and matrix effect was corrected by using two isotope-labeled standard peptides. The method exhibited good linearity in the range of 1-200 nM, with coefficients of determination of R2 > 0.998. A high sensitivity was observed, with a limit of quantification of 0.97 nM. Mean recoveries obtained from different rice matrices ranged from 82.7%-98.1% with precision <8.5% in intraday trials ( n = 6), while mean recoveries were from 75.1%-107.4% with precision <14.6% in interday trials ( n = 14). The developed method was successfully applied to the analysis of allergen Glb33 in 24 different rice cultivars.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Péptidos / Proteínas de Plantas / Oryza / Alérgenos / Cromatografía Liquida / Espectrometría de Masas en Tándem Tipo de estudio: Evaluation_studies Idioma: En Revista: J Agric Food Chem Año: 2019 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Péptidos / Proteínas de Plantas / Oryza / Alérgenos / Cromatografía Liquida / Espectrometría de Masas en Tándem Tipo de estudio: Evaluation_studies Idioma: En Revista: J Agric Food Chem Año: 2019 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos