Protein Chemistry. Structure, Properties, Research Methods - Shendryk A.N. 2022
Methods for Experimental Investigation of Protein Structure
Electron Impact Mass Spectrometry
Introduction to Deuterium-Labeled Peptides
To improve the reliability of determining the Amino Acid Sequence of a peptide, deuterium labels are introduced into it. To obtain deuterated peptide derivatives, D6-acetic anhydride or D3-methyl iodide is used instead of conventional Acetylation and methylation Reagents. Let us consider the practical implications of such a modification. For example, the ion with m/z=126 in THE SPECTRUM OF a conventional permethylated acetylpeptide may belong to an N-terminal pyrrolidonecarboxylic acid residue, an asparagine residue (resulting from N-C bond Cleavage), or an N-terminal Serine residue that has eliminated an ethanol molecule. Analysis of the D-labeled peptide analogue allows this problem to be unambiguously resolved. If the peptide is modified with unlabeled methyl iodide and D6-acetic anhydride, the mass of the ion will remain unchanged in the first two cases, while in the third case, the mass of the ion with m/z=126 will increase to 129. If D3-methyl iodide and unlabeled acetic anhydride are used, ions with m/z = 129 will be formed in the first two cases, and with m/z=132 in the third.
Last update: 06/08/2026
Editorial and Educational Adaptation: This material has been compiled based on the primary/original source text. The project team performed an editorial review, corrected technical inaccuracies, structured sections, and adapted the content for an educational format.
What was processed:
- elimination of formatting defects (OCR errors, structural breaks, corrupted characters);
- editorial organization of content;
- standardization of terminology in accordance with academic sources;
- verification of factual statements against the original source text.
All mentions of the author, publication year, and origin of the primary text have been preserved in accordance with the source.