: Terminal amine isotopic labeling of substrates (TAILS), our recently introduced platform for quantitative N-terminome analysis, enables wide dynamic range identification of original mature protein N-termini and protease cleavage products. Modifying TAILS by use of isobaric tag for relative and absolute quantification (iTRAQ)-like labels for quantification together with a robust statistical classifier derived from experimental protease cleavage data, we report reliable and statistically valid identification of proteolytic events in complex biological systems in MS2 mode. The statistical classifier is supported by a novel parameter evaluating ion intensity-dependent quantification confidences of single peptide quantifications, the quantific...
Genes encode the information for the amino acid backbone of proteins. This information can be altere...
Proteolytic processing is the most ubiquitous post-translational modification and regulator of prote...
Rapid improvements in instrumentation and data analysis make mass spectrometry-based proteomics the ...
: Terminal amine isotopic labeling of substrates (TAILS), our recently introduced platform for quant...
Analysis of the sequence and nature of protein N termini has many applications. Defining the termini...
Proteolysis is a major protein posttranslational modifica-tion that, by altering protein structure, ...
We present here a novel proteomics design for system-atic identification of protease cleavage events...
Proteases play a central role in various biochemical pathways catalyzing and regulating key biologic...
The sequence and nature of all the protein amino-termini (N-termini) within the proteome (the N-term...
Protein N termini are a unique window to the functional state of the proteome, revealing translation...
Here a workflow is proposed for the improved identification of proteolytic cleavage products using f...
Proteolysis is a critical modification leading to alteration of protein function with important outc...
iINTRODUCTION Proteases constitute 1%–5 % of eukaryotic genomes, with the human genome, in particula...
Protein N termini unambiguously identify truncated, alternatively translated or modified proteoforms...
Data analysis in proteomics is complex and with the extra challenges involved in the interpretation ...
Genes encode the information for the amino acid backbone of proteins. This information can be altere...
Proteolytic processing is the most ubiquitous post-translational modification and regulator of prote...
Rapid improvements in instrumentation and data analysis make mass spectrometry-based proteomics the ...
: Terminal amine isotopic labeling of substrates (TAILS), our recently introduced platform for quant...
Analysis of the sequence and nature of protein N termini has many applications. Defining the termini...
Proteolysis is a major protein posttranslational modifica-tion that, by altering protein structure, ...
We present here a novel proteomics design for system-atic identification of protease cleavage events...
Proteases play a central role in various biochemical pathways catalyzing and regulating key biologic...
The sequence and nature of all the protein amino-termini (N-termini) within the proteome (the N-term...
Protein N termini are a unique window to the functional state of the proteome, revealing translation...
Here a workflow is proposed for the improved identification of proteolytic cleavage products using f...
Proteolysis is a critical modification leading to alteration of protein function with important outc...
iINTRODUCTION Proteases constitute 1%–5 % of eukaryotic genomes, with the human genome, in particula...
Protein N termini unambiguously identify truncated, alternatively translated or modified proteoforms...
Data analysis in proteomics is complex and with the extra challenges involved in the interpretation ...
Genes encode the information for the amino acid backbone of proteins. This information can be altere...
Proteolytic processing is the most ubiquitous post-translational modification and regulator of prote...
Rapid improvements in instrumentation and data analysis make mass spectrometry-based proteomics the ...