Primary sequence and site-selective hydroxylation of prolines in isoforms of a major peanut allergen protein Ara h 2

被引:43
作者
Li, Jinxi [1 ]
Shefcheck, Kevin [2 ]
Callahan, John [2 ]
Fenselau, Catherine [1 ]
机构
[1] Univ Maryland, Dept Chem & Biochem, College Pk, MD 20742 USA
[2] CFSAN Food & Drug Adm, College Pk, MD 20740 USA
关键词
peanut antigen; de novo sequencing; tandem mass spectrometry; post-translational modifications; MASS-SPECTROMETRY; ARA-H-2;
D O I
10.1002/pro.295
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:174 / 182
页数:9
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