Subfemtomole MS and MS/MS peptide sequence analysis using nano-HPLC micro-ESI Fourier transform ion cyclotron resonance mass spectrometry

Citation
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
Citations number
79
Categorie Soggetti
Chemistry & Analysis","Spectroscopy /Instrumentation/Analytical Sciences
Journal title
ANALYTICAL CHEMISTRY
ISSN journal
00032700 → ACNP
Volume
72
Issue
18
Year of publication
2000
Pages
4266 - 4274
Database
ISI
SICI code
0003-2700(20000915)72:18<4266:SMAMPS>2.0.ZU;2-1
Abstract
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).