The on-line electrochemical tagging (EC-tagging) of cysteine residues in proteins during mass spectrometry is studied to probe the cysteine environment. Benzoquinone probes electrogenerated at a microspray electrode react with the thiol functions of the proteins within a microchannel and the products are analyzed by mass spectrometry. The fundamentals of the technique are discussed, with a focus on the kinetic aspects. The EC-tagging efficiency of the cysteine residues in proteins is used to probe their environment. Experiments with unmodified proteins and their chemically reduced forms highlight the strong effect of the cysteine site reactivity on the tagging efficiencies. This study highlights relevant parameters for such on-line electroc...
N-(2-Ferroceneethyl)maleimide (FEM) is introduced as an electroactive derivatizing agent for thiol f...
Cysteine-containing peptide oxidation was studied both by using an inert platinum electrode and a sa...
abstract: Significance: Modification of cysteine thiols dramatically affects protein function and st...
We present herein a review of our work on the on-line electrochemical generation of mass tags toward...
A recently developed nanospray interface for mass spectrometry (MS) was used to electro-generate ben...
Amino acid-tagging strategies are widespread in proteomics. Because of the central role of mass spec...
Redox potential, a measure of how oxidising or reducing an environment is, is tightly regulated by ...
The identification of the reaction product species stands out as one of the main limitations of the ...
Reversible thiol oxidation of cysteine residues occurs in many intracellular catalytic and signaling...
Cysteine redox state has been identified as one of the key biological influences behind protein stru...
Thesis advisor: Eranthie WeerapanaCysteine residues on proteins play important catalytic and regulat...
Die oxidative Transformation der Thiol-Gruppe des Cysteins in verschiedene andere funktionelle Grupp...
AbstractBackground: Analysis of global changes in gene transcription and translation by systems-base...
Cysteine residues on proteins serve a variety of catalytic and regulatory functions due to the high ...
Proteomic profiling using bioorthogonal chemical probes that selectively react with certain amino ac...
N-(2-Ferroceneethyl)maleimide (FEM) is introduced as an electroactive derivatizing agent for thiol f...
Cysteine-containing peptide oxidation was studied both by using an inert platinum electrode and a sa...
abstract: Significance: Modification of cysteine thiols dramatically affects protein function and st...
We present herein a review of our work on the on-line electrochemical generation of mass tags toward...
A recently developed nanospray interface for mass spectrometry (MS) was used to electro-generate ben...
Amino acid-tagging strategies are widespread in proteomics. Because of the central role of mass spec...
Redox potential, a measure of how oxidising or reducing an environment is, is tightly regulated by ...
The identification of the reaction product species stands out as one of the main limitations of the ...
Reversible thiol oxidation of cysteine residues occurs in many intracellular catalytic and signaling...
Cysteine redox state has been identified as one of the key biological influences behind protein stru...
Thesis advisor: Eranthie WeerapanaCysteine residues on proteins play important catalytic and regulat...
Die oxidative Transformation der Thiol-Gruppe des Cysteins in verschiedene andere funktionelle Grupp...
AbstractBackground: Analysis of global changes in gene transcription and translation by systems-base...
Cysteine residues on proteins serve a variety of catalytic and regulatory functions due to the high ...
Proteomic profiling using bioorthogonal chemical probes that selectively react with certain amino ac...
N-(2-Ferroceneethyl)maleimide (FEM) is introduced as an electroactive derivatizing agent for thiol f...
Cysteine-containing peptide oxidation was studied both by using an inert platinum electrode and a sa...
abstract: Significance: Modification of cysteine thiols dramatically affects protein function and st...