Neutron-Encoded Mass Signatures for Quantitative Top-Down Proteomics

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• 作者：Timothy W. Rhoads ; Christopher M. Rose ; Derek J. Bailey ; Nicholas M. Riley ; Rosalynn C. Molden ; Amelia J. Nestler ; Anna E. Merrill ; Lloyd M. Smith ; Alexander S. Hebert ; Michael S. Westphall ; David J. Pagliarini ; Benjamin A. Garcia ; Joshua J. Coon
• 刊名：Analytical Chemistry
• 出版年：2014
• 出版时间：March 4, 2014
• 年：2014
• 卷：86
• 期：5
• 页码：2314-2319
• 全文大小：353K
• 年卷期：v.86,no.5(March 4, 2014)
• ISSN：1520-6882

文摘

The ability to acquire highly accurate quantitative data is an increasingly important part of any proteomics experiment, whether shotgun or top-down approaches are used. We recently developed a quantitation strategy for peptides based on neutron encoding, or NeuCode SILAC, which uses closely spaced heavy isotope-labeled amino acids and high-resolution mass spectrometry to provide quantitative data. We reasoned that the strategy would also be applicable to intact proteins and could enable robust, multiplexed quantitation for top-down experiments. We used yeast lysate labeled with either ¹³C₆¹⁵N₂-lysine or ²H₈-lysine, isotopologues of lysine that are spaced 36 mDa apart. Proteins having such close spacing cannot be distinguished during a medium resolution scan, but upon acquiring a high-resolution scan, the two forms of the protein with each amino acid are resolved and the quantitative information revealed. An additional benefit NeuCode SILAC provides for top down is that the spacing of the isotope peaks indicates the number of lysines present in the protein, information that aids in identification. We used NeuCode SILAC to quantify several hundred isotope distributions, manually identify and quantify proteins from 1:1, 3:1, and 5:1 mixed ratios, and demonstrate MS²-based quantitation using ETD.