Mid-Infrared Spectroscopy for the Qualitative and Quantitative Analysis of the Wheat Proteome

Wheat contributes 19% of protein in the global human diet. Mid-infrared spectroscopy (MIR) combined with attenuated total reflection (ATR) is an excellent analytical method for assessing the chemical composition of complex biological samples. In contrast to established techniques used for wheat protein analysis, we show that by using ATR-MIR the protein secondary structures of different fractions can be studied. We found that albumin and globulin fractions were primarily composed of α-helix, with proportions of 57.8% and 45.9%, respectively. Gliadins, meanwhile, contained 38.3% β-turn and 36.9% α-helix, while glutenins predominantly exhibited 44.8% β-turn secondary structures. In addition, we found that by using analysis of variance (ANOVA) simultaneous component analysis (ASCA), the obtained MIR spectra of the wheat protein fractions were significantly (<i>p</i> < 0.001) affected by the sampling sites and variety. Quantification of the protein content of each sample through the amide II band also revealed significant differences (<i>p</i> < 0.001) across the sampling sites in the different protein fractions. The found concentration range of protein fractions within the wheat samples were as follows: 1.7-3.6, 0.4-2.4, 4.0-5.4, and 0.8-4.8 g/100 g of albumins, globulins, gliadins, and glutenins, respectively. In conclusion, this study shows that ATR-MIR has an immense potential for wheat proteome analysis.

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Journal
Analytical Chemistry
Published
2026-01-21
DOI
https://doi.org/10.1021/acs.analchem.5c05258
Primary Topic
Spectroscopy and Chemometric Analyses
Type
article
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article

Mid-Infrared Spectroscopy for the Qualitative and Quantitative Analysis of the Wheat Proteome

Elisabeth Reiter, Stephan Freitag, Dedy Leonardo Nadeak, Sabine Baumgartner et al.
Analytical Chemistry
Spectroscopy and Chemometric Analyses
article

Mid-Infrared Spectroscopy for the Qualitative and Quantitative Analysis of the Wheat Proteome

Elisabeth Reiter, Stephan Freitag, Dedy Leonardo Nadeak, Sabine Baumgartner, Rudolf Krska, Michael Wiederstein
article en

Abstract

Wheat contributes 19% of protein in the global human diet. Mid-infrared spectroscopy (MIR) combined with attenuated total reflection (ATR) is an excellent analytical method for assessing the chemical composition of complex biological samples. In contrast to established techniques used for wheat protein analysis, we show that by using ATR-MIR the protein secondary structures of different fractions can be studied. We found that albumin and globulin fractions were primarily composed of α-helix, with proportions of 57.8% and 45.9%, respectively. Gliadins, meanwhile, contained 38.3% β-turn and 36.9% α-helix, while glutenins predominantly exhibited 44.8% β-turn secondary structures. In addition, we found that by using analysis of variance (ANOVA) simultaneous component analysis (ASCA), the obtained MIR spectra of the wheat protein fractions were significantly (<i>p</i> < 0.001) affected by the sampling sites and variety. Quantification of the protein content of each sample through the amide II band also revealed significant differences (<i>p</i> < 0.001) across the sampling sites in the different protein fractions. The found concentration range of protein fractions within the wheat samples were as follows: 1.7-3.6, 0.4-2.4, 4.0-5.4, and 0.8-4.8 g/100 g of albumins, globulins, gliadins, and glutenins, respectively. In conclusion, this study shows that ATR-MIR has an immense potential for wheat proteome analysis.

Analytical ChemistryVol. 98(4)
Queen's University Belfast (GB), Institute for Security Studies (KE), Bioanalytica (Switzerland) (CH), Feed Control (Norway) (NO), Agency for Quality Assurance and Accreditation Austria (AT), Austrian Agency for Health and Food Safety (AT)
Zero hunger
Openalex Percentile: Top 82%
Spectroscopy and Chemometric Analyses
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Mid-Infrared Spectroscopy for the Qualitative and Quantitative Analysis of the Wheat Proteome — Elisabeth Reiter, Stephan Freitag, et al. · Analytical Chemistry (2026) | TGRS Research Map | TGRS