AI Article Synopsis

  • The study discusses using iodoacetamide (IAA) and N-methyliodoacetamide (MIAA) as labeling agents for measuring proteins via MALDI-MS, which simplifies the process compared to isotope labeling.
  • These reagents specifically target cysteine residues in proteins during denaturation and digestion, showing effective dynamic ranges and high correlation coefficients for quantifying proteins like lysozyme, transferrin, and BSA.
  • The labeling method is particularly advantageous for relative quantification in cases where the chromatographic isotope effect isn't a significant issue.

Article Abstract

The use of iodoacetamide (IAA) and N-methyliodoacetamide (MIAA) as labeling agents for the relative measurements of proteins using MALDI-MS is described herein. These reagents, which alkylate the thiol groups of cysteine residues in proteins, were introduced during the alkylation step of a common protein denaturation and digestion process. This approach is simpler and cheaper than those involving isotope labeling agents. The labeling agents described herein displayed good dynamic ranges and correlation coefficients for protein quantification analyses when the proteins were treated through either in-solution or in-gel digestion. The best dynamic ranges (in the molar ratio) for proteins lysozyme, transferrin, and BSA (in-solution digestion) are 0.1-10, 0.1-8, and 0.1-8, respectively. The corresponding correlation coefficients are greater than 0.99. The IAA/MIAA labeling is a useful method for the relative quantification of peptides and digested proteins when the chromatographic isotope effect is not a major concern.

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http://dx.doi.org/10.1002/jssc.200700440DOI Listing

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