A Selenium-based Cysteine Surrogate for ...
Document type :
Partie d'ouvrage: Chapitre
Title :
A Selenium-based Cysteine Surrogate for Protein Chemical Synthesis
Author(s) :
Firstova, Olga [Auteur]
Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Agouridas, Vangelis [Auteur]
Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Diemer, Vincent [Auteur]
Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Melnyk, Oleg [Auteur]
Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Agouridas, Vangelis [Auteur]

Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Diemer, Vincent [Auteur]
Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Melnyk, Oleg [Auteur]
Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Scientific editor(s) :
Xuechen Li
Book title :
Chemical Protein Synthesis
Publisher :
Springer
Publication date :
2022
ISBN :
978-1-0716-2488-3
English keyword(s) :
N-(2-selenoethyl)cysteine
cysteine surrogate
native chemical ligation (NCL)
bis(2- sulfanylethyl)amido (SEA)-mediated ligation
chemical protein synthesis
sulfur
selenium
one-pot
cysteine surrogate
native chemical ligation (NCL)
bis(2- sulfanylethyl)amido (SEA)-mediated ligation
chemical protein synthesis
sulfur
selenium
one-pot
HAL domain(s) :
Chimie/Chimie organique
English abstract : [en]
N-selenoethyl cysteine (SetCys) in the form of its cyclic selenosulfide is a cysteine surrogate, whose reactivity depends on the reducing power of the medium. SetCys does not interfere with the native chemical ligation ...
Show more >N-selenoethyl cysteine (SetCys) in the form of its cyclic selenosulfide is a cysteine surrogate, whose reactivity depends on the reducing power of the medium. SetCys does not interfere with the native chemical ligation reaction under mild reducing conditions, that is in the absence of tris(2-carboxyethyl)phosphine (TCEP). In contrast, subjecting SetCys to TCEP results in the spontaneous loss of its N-selenoethyl appendage and thus to its conversion into a Cys residue. Therefore, SetCys can be used for the redox-controlled assembly of peptide segments using NCL. We provide in this protocol detailed procedures for the synthesis of Fmoc-protected SetCys residue and for its incorporation into peptides using standard solid-phase peptide synthesis protocols. We also describe its use for the chemical synthesis of proteins through the redox-controlled assembly of three peptide segments in one-pot.Show less >
Show more >N-selenoethyl cysteine (SetCys) in the form of its cyclic selenosulfide is a cysteine surrogate, whose reactivity depends on the reducing power of the medium. SetCys does not interfere with the native chemical ligation reaction under mild reducing conditions, that is in the absence of tris(2-carboxyethyl)phosphine (TCEP). In contrast, subjecting SetCys to TCEP results in the spontaneous loss of its N-selenoethyl appendage and thus to its conversion into a Cys residue. Therefore, SetCys can be used for the redox-controlled assembly of peptide segments using NCL. We provide in this protocol detailed procedures for the synthesis of Fmoc-protected SetCys residue and for its incorporation into peptides using standard solid-phase peptide synthesis protocols. We also describe its use for the chemical synthesis of proteins through the redox-controlled assembly of three peptide segments in one-pot.Show less >
Language :
Anglais
Audience :
Internationale
Popular science :
Non
Source :
Files
- document
- Open access
- Access the document
- a-selenium-based-cysteine-surrogate-for-protein-chemical-synthesis.pdf
- Open access
- Access the document
- document
- Open access
- Access the document
- a-selenium-based-cysteine-surrogate-for-protein-chemical-synthesis.pdf
- Open access
- Access the document