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A proteomic approach to verify in vivo expression of a novel gamma-gliadin containing an extra cysteine residue.

TitleA proteomic approach to verify in vivo expression of a novel gamma-gliadin containing an extra cysteine residue.
Publication TypeArticolo su Rivista peer-reviewed
Year of Publication2006
AuthorsFerrante, Paola, Masci Stefania, D’Ovidio Renato, Lafiandra Domenico, Volpi Chiara, and Mattei Benedetta
JournalProteomics
Volume6
Pagination1908-14
Date Published2006 Mar
ISSN1615-9853
KeywordsAmino Acid Sequence, Blotting, Chromatography, Cloning, Conserved Sequence, Cystine, Electrophoresis, Escherichia coli, Flour, Gel, Gene expression, Genes, Genetic Vectors, Gliadin, Glutens, High Pressure Liquid, Inclusion Bodies, Mass, Mass Spectrometry, Matrix-Assisted Laser Desorption-Ionization, Molecular, Molecular Sequence Data, Molecular Weight, Peptide Hydrolases, Peptide Mapping, Plant, Polyacrylamide Gel, Proteomics, Spectrometry, Triticum, Two-Dimensional, Western
Abstract

Gliadins and glutenins are the main protein fractions present in wheat gluten. They are responsible for technological and nutritional quality of wheat based products. In particular, glutenins are mainly responsible for dough visco-elastic properties, whereas gliadins confer extensibility to dough and are the most important factor triggering celiac disease, the major human intolerance to gluten. Gliadins are monomeric proteins, whereas glutenins are polymers stabilized by disulfide bonds. Although they have distinctive structural characteristics, it is possible that some gliadins become part of the glutenin fraction because of mutations that affect cysteine number and distribution. Here, we provide evidence that a naturally mutated gamma-gliadin with an extra cysteine residue is incorporated into the polymeric fraction. This goal was achieved using an integrated approach involving heterologous expression, 2-DE, RP-HPLC and MS.

Citation Key1217