We present a precursor ion independent top-down algorithm (PIITA) for use in automated assignment of protein identifications from tandem mass spectra of whole proteins. To acquire the data, we utilize data-dependent acquisition to select protein precursor ions eluting from a C4-based HPLC column for collision induced dissociation in the linear ion trap of an LTQ-Orbitrap mass spectrometer. Gas-phase fractionation is used to increase the number of acquired tandem mass spectra, all of which are recorded in the Orbitrap mass analyzer. To identify proteins, the PIITA algorithm compares deconvoluted, deisotoped, observed tandem mass spectra to all possible theoretical tandem mass spectra for each protein in a genomic sequence database without re...
Abstract Background High-resolution tandem mass spectra can now be readily acquired with hybrid ins...
Data-independent mass spectrometry activates all ion species isolated within a given mass-to-charge ...
In bottom-up proteomics, peptides are separated by liquid chromatography with elution peak widths in...
We present a precursor ion independent top-down algorithm (PIITA) for use in automated assignment of...
Owing to the development of electrospray ionization (ESI), various ion dissociation techniques and s...
Mass spectrometry is the major analytical tool for the identification and quantification of proteins...
A simple procedure is described that increases sensitivity and dynamic range for the analysis of a p...
The most widely used modern mass spectrometers face severe performance limitations with molecules la...
Proteomics has exposed a plethora of posttranslational modifications, but demonstrating functional r...
Conventional TopN data-dependent acquisition (DDA) LC–MS/MS analysis identifies only a limited fract...
Currently, the precursor ion selection strategies in LC-MS mainly choose the most prominent peptide ...
Tandem mass spectrometry has been utilized in the field of proteomics to identify and characterize p...
Currently, the precursor ion selection strategies in LC-MS mainly choose the most prominent peptide ...
AbstractQuadrupole ion trap scanning parameters for performing bottom-up proteomics in a data-depend...
The goal of proteomics research is to be able to identify and quantify the vast numbers of proteins ...
Abstract Background High-resolution tandem mass spectra can now be readily acquired with hybrid ins...
Data-independent mass spectrometry activates all ion species isolated within a given mass-to-charge ...
In bottom-up proteomics, peptides are separated by liquid chromatography with elution peak widths in...
We present a precursor ion independent top-down algorithm (PIITA) for use in automated assignment of...
Owing to the development of electrospray ionization (ESI), various ion dissociation techniques and s...
Mass spectrometry is the major analytical tool for the identification and quantification of proteins...
A simple procedure is described that increases sensitivity and dynamic range for the analysis of a p...
The most widely used modern mass spectrometers face severe performance limitations with molecules la...
Proteomics has exposed a plethora of posttranslational modifications, but demonstrating functional r...
Conventional TopN data-dependent acquisition (DDA) LC–MS/MS analysis identifies only a limited fract...
Currently, the precursor ion selection strategies in LC-MS mainly choose the most prominent peptide ...
Tandem mass spectrometry has been utilized in the field of proteomics to identify and characterize p...
Currently, the precursor ion selection strategies in LC-MS mainly choose the most prominent peptide ...
AbstractQuadrupole ion trap scanning parameters for performing bottom-up proteomics in a data-depend...
The goal of proteomics research is to be able to identify and quantify the vast numbers of proteins ...
Abstract Background High-resolution tandem mass spectra can now be readily acquired with hybrid ins...
Data-independent mass spectrometry activates all ion species isolated within a given mass-to-charge ...
In bottom-up proteomics, peptides are separated by liquid chromatography with elution peak widths in...