Cysteine Thiol Modification

Cysteine thiol modification is the chemical alteration of cysteine residues through reactions involving their sulfur-containing thiol groups, providing a way to regulate protein structure and function. Because thiols can act as nucleophiles, they undergo reversible oxidation to disulfides, sulfenic acids, or other redox states, as well as covalent alkylation by electrophilic compounds; their reactivity depends on factors such as pH and local protein environment. In immunology and infection research, these modifications help reveal how oxidative stress, host defense pathways, and pathogen-derived molecules alter signaling proteins, enzymes, and virulence factors. Analytical and labeling methods for cysteine modification therefore support studies of redox biology, immune regulation, and therapeutic target development.

Cysteine Thiol Modification - Related Videos

Research

JoVE Journal - Immunology and Infection

Targeting Cysteine Thiols for in Vitro Site-specific Glycosylation of Recombinant Proteins

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Cited by 1 •

2017

Biochemical and structural analyses of glycosylated proteins require relatively large amounts of homogeneous samples. Here, we present an efficient chemical method for site-specific glycosylation of recombinant proteins purified from bacteria by targeting reactive Cys thiols.

Synthesis of Protein Bioconjugates via Cysteine-maleimide Chemistry

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Cited by 8 •

2016

This protocol details the important steps required for the bioconjugation of a cysteine containing protein to a maleimide, including reagent purification, reaction conditions, bioconjugate purification and bioconjugate characterization.

Analysis of the Solvent Accessibility of Cysteine Residues on Maize rayado fino virus Virus-like Particles Produced in Nicotiana benthamiana Plants and Cross-linking of Peptides to VLPs

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Cited by 3 •

2013

A method to analyze the solvent accessibility of the thiol group of cysteine residues of Maize rayado fino virus (MRFV)-virus-like particles (VLPs) followed by a peptide cross-linking reaction is described. The method takes advantage of the availability of several chemical groups on the surface of the VLPs that can be targets for specific reactions.

Research

JoVE Journal - Biology
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Profiling Thiol Redox Proteome Using Isotope Tagging Mass Spectrometry

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Cited by 50 •

2012

Reactive oxygen species level is elevated when cells encounter stress conditions. Here we show the example of 3'-3' diaminobenzidine staining as well as cysTMT labeling and mass spectrometry to profile the redox proteome in Pseudomonas syringae treated tomato leaves.

Labeling of Surface-Accessible Cysteine Residues in Engineered Virus-Like Particles

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2026

Source: Natilla, A.,and Hammond, R. W. Analysis of the Solvent Accessibility of Cysteine Residues on Maize rayado fino virus Virus-like Particles Produced in Nicotiana benthamiana Plants and Cross-linking of Peptides to VLPs. J. Vis. Exp. (2013)This video demonstrates site-specific fluorescent labeling of mutant virus-like particles (VLPs) produced in Nicotiana benthamiana using a thiol-reactive dye, followed by purification and gel electrophoresis to confirm surface modification.

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