Rapid Online Nonenzymatic Protein Digestion Combining Microwave Heating Acid Hydrolysis and Electrochemical Oxidation

被引:21
作者
Basile, Franco [1 ]
Hauser, Nicolas [1 ]
机构
[1] Univ Wyoming, Dept Chem, Laramie, WY 82071 USA
基金
美国国家卫生研究院;
关键词
MASS-SPECTROMETRIC DETECTION; TYROSYL-PEPTIDE BONDS; MEMBRANE-PROTEINS; ASPARTIC-ACID; CNBR CLEAVAGE; RESIDUES; DISSOCIATION; TRYPTOPHAN; PROTEOMICS; SITE;
D O I
10.1021/ac1024705
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We report an online nonenzymatic method for site-specific digestion of proteins to yield peptides that are well suited for collision-induced dissociation tandem mass spectrometry. The method combines online microwave heating acid hydrolysis at aspartic acid and online electrochemical oxidation at tryptophan and tyrosine. The combined microwave/electrochemical digestion is reproducible and produces peptides with an average sequence length of 10 amino acids. This peptide length is similar to the average peptide length of 9 amino acids obtained by digestion of proteins with the enzyme trypsin. As a result, the peptides produced by this novel nonenzymatic digestion method, when analyzed by electrospray ionization mass spectrometry, produce protonated molecules with mostly +1 and +2 charge states. The combination of these two nonenzymatic methods overcomes shortcomings with each individual method in that (i) peptides generated by the microwave-hydrolysis method have an average amino acid length of 16 amino acids and (ii) the electrochemical-cleavage method is unable to reproducibly digest proteins with molecular masses above 4 kDa. Preliminary results are presented on the application and utility of this rapid online digestion (total of 6 mm of digestion time) on a series of standard peptides and proteins as well as an Escherichia coli protein extract.
引用
收藏
页码:359 / 367
页数:9
相关论文
共 31 条