RRC ID 4956
Author Ebhardt HA, Xu Z, Fung AW, Fahlman RP.
Title Quantification of the post-translational addition of amino acids to proteins by MALDI-TOF mass spectrometry.
Journal Anal Chem
Abstract Aminoacyl-tRNA protein transferases catalyze the post-translational addition of amino acids to proteins. The eubacterial leucyl/phenylalanyl-tRNA-protein transferase (L/F transferase) catalyzes the transfer of leucine or phenylalanine from their respective aminoacylated tRNAs to the N-termini of substrate proteins possessing an N-terminal lysine or arginine amino acid. Conventional assays to quantify L/F transferase activity involve measuring radioactive amino acid incorporation into substrate proteins. We have developed a quantitative matrix assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry procedure to measure the enzymatic activity of L/F transferase. The procedure utilizes stable isotope labeled substrate and internal standard peptides. The method is used to determine the kinetic parameters of k(cat) and K(m) for the enzymatic transfer of phenylalanine and three unnatural amino acid derivatives from an aminoacyl-tRNA to a peptide substrate.
Volume 81(5)
Pages 1937-43
Published 2009-3-1
DOI 10.1021/ac802423d
PII 10.1021/ac802423d
PMID 19186990
MeSH Amino Acids / chemistry* Protein Processing, Post-Translational* Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization / methods* Transferases / metabolism
IF 6.785
Times Cited 10
WOS Category CHEMISTRY, ANALYTICAL
Resource
Prokaryotes E. coli ASKA(-) collection?