Selecting protein N-terminal peptides by combined fractional diagonal chromatography. - Wikidata - awgldk - TriplyDB

Selecting protein N-terminal peptides by combined fractional diagonal chromatography.

Selecting protein N-terminal peptides by combined fractional diagonal chromatography.

http://www.wikidata.org/entity/Q49052034

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N-terminal acetylome analysis reveals the specificity of Naa50 (Nat5) and suggests a kinetic competition between N-terminal acetyltransferases and methionine aminopeptidases.Protein N-terminal acetyltransferases act as N-terminal propionyltransferases in vitro and in vivo.Proteomic Substrate Identification for Membrane Proteases in the Brain Biochemical and cellular analysis of Ogden syndrome reveals downstream Nt-acetylation defects A Saccharomyces cerevisiae model reveals in vivo functional impairment of the Ogden syndrome N-terminal acetyltransferase NAA10 Ser37Pro mutant Mapping proteolytic processing in the secretome of gastric cancer-associated myofibroblasts reveals activation of MMP-1, MMP-2, and MMP-3 An improved workflow for quantitative N-terminal charge-based fractional diagonal chromatography (ChaFRADIC) to study proteolytic events in Arabidopsis thaliana.Proteome-derived peptide libraries to study the substrate specificity profiles of carboxypeptidases.Granzyme M targets topoisomerase II alpha to trigger cell cycle arrest and caspase-dependent apoptosis.N-terminal proteomics and ribosome profiling provide a comprehensive view of the alternative translation initiation landscape in mice and men N-Terminal-oriented proteogenomics of the marine bacterium roseobacter denitrificans Och114 using N-Succinimidyloxycarbonylmethyl)tris(2,4,6-trimethoxyphenyl)phosphonium bromide (TMPP) labeling and diagonal chromatography.N-terminal Proteomics Assisted Profiling of the Unexplored Translation Initiation Landscape in Arabidopsis thaliana PROTEOFORMER: deep proteome coverage through ribosome profiling and MS integration Importance of extended protease substrate recognition motifs in steering BNIP-2 cleavage by human and mouse granzymes B.The Apaf-1-binding protein Aven is cleaved by Cathepsin D to unleash its anti-apoptotic potential Unbiased selective isolation of protein N-terminal peptides from complex proteome samples using phospho tagging (PTAG) and TiO(2)-based depletion Quantitative proteomics analysis of the Arg/N-end rule pathway of targeted degradation in Arabidopsis roots New approaches for dissecting protease functions to improve probe development and drug discovery Absence of N-terminal acetyltransferase diversification during evolution of eukaryotic organisms.Positional proteomics reveals differences in N-terminal proteoform stability.The DegraBase: a database of proteolysis in healthy and apoptotic human cells Mutant methionyl-tRNA synthetase from bacteria enables site-selective N-terminal labeling of proteins expressed in mammalian cells.How many signal peptides are there in bacteria?Quantitative MS-based enzymology of caspases reveals distinct protein substrate specificities, hierarchies, and cellular roles.Deep proteome coverage based on ribosome profiling aids mass spectrometry-based protein and peptide discovery and provides evidence of alternative translation products and near-cognate translation initiation events Comprehensive identification of translation start sites by tetracycline-inhibited ribosome profiling Matrix metalloproteinase 13 modulates intestinal epithelial barrier integrity in inflammatory diseases by activating TNF.ADAM30 Downregulates APP-Linked Defects Through Cathepsin D Activation in Alzheimer's Disease.Protein alpha-N-acetylation studied by N-terminomics.Proteogenomics for environmental microbiology.Matrix metalloproteinase processing of signaling molecules to regulate inflammation.Mapping orphan proteases by proteomics: meprin metalloproteases deciphered as potential therapeutic targets.N-terminomics and proteogenomics, getting off to a good start.Proteogenomics in microbiology: taking the right turn at the junction of genomics and proteomics.The proteome under translational control.Fast profiling of protease specificity reveals similar substrate specificities for cathepsins K, L and S.The application of terminomics for the identification of protein start sites and proteoforms in bacteria.Identification of Serpinb6b as a species-specific mouse granzyme A inhibitor suggests functional divergence between human and mouse granzyme A.Comprehensive analysis of human protein N-termini enables assessment of various protein forms.Proteogenomics from a bioinformatics angle: A growing field.

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P2860

Selecting protein N-terminal peptides by combined fractional diagonal chromatography.

http://www.wikidata.org/entity/Q49052034

description

2011 nî lūn-bûn

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2011年の論文

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年學術文章

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2011年學術文章

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name

Selecting protein N-terminal peptides by combined fractional diagonal chromatography.

@en

Selecting protein N-terminal peptides by combined fractional diagonal chromatography.

@nl

type

label

Selecting protein N-terminal peptides by combined fractional diagonal chromatography.

@en

Selecting protein N-terminal peptides by combined fractional diagonal chromatography.

@nl

prefLabel

Selecting protein N-terminal peptides by combined fractional diagonal chromatography.

@en

Selecting protein N-terminal peptides by combined fractional diagonal chromatography.

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Nature Protocols

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Selecting protein N-terminal peptides by combined fractional diagonal chromatography.

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Bart Ruttens

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Evy Timmerman

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Francis Impens

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Hans Demol

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Joël Vandekerckhove

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Kris Gevaert

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Marc Goethals

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P2860

Composition and biological significance of the human Nα-terminal acetyltransferases

OpenMS - an open-source software framework for mass spectrometry

Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides

Proteome-wide Identification of HtrA2/Omi Substrates

Global sequencing of proteolytic cleavage sites in apoptosis by specific labeling of protein N termini

Profiling constitutive proteolytic events in vivo

Structure of granzyme C reveals an unusual mechanism of protease autoinhibition

Global analysis of the mitochondrial N-proteome identifies a processing peptidase critical for protein stability.

Stable isotope labeling by amino acids in cell culture, SILAC, as a simple and accurate approach to expression proteomics

Open mass spectrometry search algorithm

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10.1038/NPROT.2011.355

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8

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6

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Petra Van Damme

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2011-07-14T00:00:00Z

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21799483

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