Se. Martin et al., Subfemtomole MS and MS/MS peptide sequence analysis using nano-HPLC micro-ESI Fourier transform ion cyclotron resonance mass spectrometry, ANALYT CHEM, 72(18), 2000, pp. 4266-4274
Subfemtomole peptide sequence analysis has been achieved using microcapilla
ry HPLC columns, with integrated nanoelectrospray emitters, coupled directl
y to a Fourier transform ion cyclotron resonance mass spectrometer. Accurat
e mass (+/-0.010 Da) peptide maps are generated from a standard six-protein
digest mixture, whose principle components span a concentration dynamic ra
nge of 1000:1. Iterative searches against similar to 189 000 entries in the
OWL database readily identify each protein, with high sequence coverage (2
0-60%), from as little as 10 amol loaded on-column. In addition, a simple v
ariable-flow HPLC apparatus provides for on-line tandem mass spectrometric
analysis of tryptic peptides at the 400-amol level. MS/MS data are searched
against similar to 280 000 entries in a nonredundant protein database usin
g SEQUEST. Accurate precursor and product ion mass information readily iden
tifiers primary amino acid sequences differing by:asparagine vs aspartic ac
id (Delta m = 0.98 Da) and glutamine vs lysine (Delta m = 0.036 Da).