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Thiol Catalysis of Selenosulfide Bond Cleavage by a Triarylphosphine.
Firstova, Olga; Melnyk, Oleg; Diemer, Vincent.
Afiliação
  • Firstova O; Univ. Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, U1019 - UMR 9017 - CIIL - Center for Infection and Immunity of Lille, F-59000 Lille, France.
  • Melnyk O; Univ. Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, U1019 - UMR 9017 - CIIL - Center for Infection and Immunity of Lille, F-59000 Lille, France.
  • Diemer V; Univ. Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, U1019 - UMR 9017 - CIIL - Center for Infection and Immunity of Lille, F-59000 Lille, France.
J Org Chem ; 87(14): 9426-9430, 2022 07 15.
Article em En | MEDLINE | ID: mdl-35763672
ABSTRACT
The arylthiol 4-mercaptophenylacetic acid (MPAA) is a powerful catalyst of selenosulfide bond reduction by the triarylphosphine 3,3',3″-phosphanetriyltris(benzenesulfonic acid) trisodium salt (TPPTS). Both reagents are water-soluble at neutral pH and are particularly adapted for working with unprotected peptidic substrates. Contrary to trialkylphosphines such as tris(2-carboxyethyl)phosphine hydrochloride (TCEP), TPPTS has the advantage of not inducing deselenization reactions. We believe that the work reported here will be of value for those manipulating selenosulfide bonds in peptidic or protein molecules.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fosfinas / Compostos de Sulfidrila Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fosfinas / Compostos de Sulfidrila Idioma: En Ano de publicação: 2022 Tipo de documento: Article