Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Reactivity-based chemical proteomics is a powerful technology based on the use of tagged chemicals that covalently react with surface-exposed residues on proteins in native proteomes. Reactivity profiling involves the purification, identification, and quantification of labeled peptides by LC-MS/MS. Here, we have detailed a protocol for reactivity profiling of Cys residues using iodoacetamide probes, displaying >1000 reactive Cys residues in the proteome of phytopathogen Pseudomonas syringae pv. tomato DC3000 (PtoDC3000). Comparative reactivity profiling of PtoDC3000 treated with or without hydrogen peroxide (H2O2) identified ~200 H2O2-sensitive Cys residues in antioxidant enzymes, metabolic enzymes, and transcription regulators. Interestingly, half of these H2O2-sensitive Cys residues are more reactive in response to H2O2 and several proteins have multiple Cys residues with opposite reactivities in response to H2O2 exposure.

Original publication

DOI

10.1007/978-1-0716-2079-3_9

Type

Journal article

Journal

Methods Mol Biol

Publication Date

2022

Volume

2447

Pages

105 - 117

Keywords

BIAM, Biotinylated iodoacetamide, Hydrogen peroxide, LC-MS/MS, Pseudomonas syringae pv. tomato DC3000, Reactivity profiling, Redox-sensitive Cys residues, Chromatography, Liquid, Cysteine, Hydrogen Peroxide, Solanum lycopersicum, Oxidation-Reduction, Proteome, Pseudomonas syringae, Tandem Mass Spectrometry