Electrospray ionization mass spectrometry (ES-MS) was utilized to accurately measure the molecular weight of uniformly l5N and 13C/15N isotope labeled stromelysin catalytic domain (20 kDa), which in turn, was used to determine the degree of isotope enrichment in the protein.
QuantiSpec — Quantitative mass spectrometry data analysis of 15N-metabolically labeled proteins
✍ Scribed by Katrin Haegler; Nikola S. Mueller; Giuseppina Maccarrone; Eva Hunyadi-Gulyas; Christian Webhofer; Michaela D. Filiou; Yaoyang Zhang; Christoph W. Turck
- Publisher
- Elsevier
- Year
- 2009
- Tongue
- English
- Weight
- 658 KB
- Volume
- 71
- Category
- Article
- ISSN
- 1874-3919
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✦ Synopsis
For relative protein quantitation by mass spectrometry we metabolically labeled E. coli bacteria with (15)N-enriched diets. Proteins extracted from (15)N-labeled and unlabeled E. coli bacteria were mixed, separated by two-dimensional gel electrophoresis and enzymatically digested. The resulting tryptic peptides were analyzed by MALDI mass spectrometry. For the relative protein quantitation we developed fully automated software, QuantiSpec (Quantitative Mass Spectrometry Analysis Software), which uses data from MALDI TOF mass spectrometry and the Mascot database search engine. QuantiSpec detects natural as well as partially or fully labeled peptide isotope distributions. For each identified peptide the (15)N incorporation rate is determined by comparing the experimental to a set of theoretical isotope patterns based on the peptide sequence. Relative quantitation is accomplished by calculating the signal intensity ratios for each (14)N/(15)N peptide pair.
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