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Primary sequence and site-selective hydroxylation of prolines in isoforms of a major peanut allergen protein Ara h 2
- Source :
- Protein Science.
- Publication Year :
- 2009
- Publisher :
- Wiley, 2009.
-
Abstract
- The Ara h 2 proteins are major determinants of peanut allergens. These proteins have not been fully studied at the molecular level. It has been previously proposed that there are two isoforms of Ara h 2, based on primary structures that were deduced from two reported cDNA sequences. In this report, four isoforms have been purified and characterized individually. Mass spectrometric methods have been used to determine the protein sequences and to define post-translational modifications for all four isoforms. Two pairs of isoforms have been identified, corresponding to a long-chain form and a form that is shorter by 12 amino acids. Each pair is further differentiated by the presence or absence of a two amino acid sequence at the carboxyl terminus of the protein. Modifications that were characterized include site-specific hydroxylation of proline residues, but no glycosylation was found, in contrast to previous reports.
- Subjects :
- Gene isoform
Glycosylation
Proline
Molecular Sequence Data
Sequence alignment
Hydroxylation
Biochemistry
chemistry.chemical_compound
Tandem Mass Spectrometry
Complementary DNA
Protein Isoforms
Amino Acid Sequence
Disulfides
Molecular Biology
Peptide sequence
Glycoproteins
chemistry.chemical_classification
Allergens
Antigens, Plant
Chromatography, Ion Exchange
Peptide Fragments
Amino acid
Molecular Weight
chemistry
Protein Structure Report
Glycoprotein
Protein Processing, Post-Translational
Sequence Alignment
2S Albumins, Plant
Subjects
Details
- ISSN :
- 1469896X and 09618368
- Database :
- OpenAIRE
- Journal :
- Protein Science
- Accession number :
- edsair.doi.dedup.....9cb682a8eb3296240959917686fa4a8d
- Full Text :
- https://doi.org/10.1002/pro.295