Literature DB >> 7459689

Amino group reactions of the sulfhydryl reagent methyl methanesulfonothioate. Inactivation of D-3-hydroxybutyrate dehydrogenase and reaction with amines in water.

R Kluger, W C Tsui.   

Abstract

Methyl methanesulfonothioate (MMTS) has been used as a sulfhydryl reagent. However, it inactivates D-3-hydroxybutyrate dehydrogenase in a manner that suggests that an amino group may have reacted with the reagent. Nuclear magnetic resonance (NMR) analysis of solutions of glycylglycine, glycine ethyl ester, and imidazole with MMTS indicates that a reaction occurs which produces what is identified by its NMR signal as the methylsulfenamide of the amine. It is suggested that caution should be used when MMTS is employed where reaction with an amine could give an undesired product.

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Year:  1980        PMID: 7459689     DOI: 10.1139/o80-086

Source DB:  PubMed          Journal:  Can J Biochem        ISSN: 0008-4018


  2 in total

1.  Protein modification by thiolactone homocysteine chemistry: a multifunctionalized human serum albumin theranostic.

Authors:  Tatyana V Popova; Olesya A Krumkacheva; Anna S Burmakova; Anna S Spitsyna; Olga D Zakharova; Vladimir A Lisitskiy; Igor A Kirilyuk; Vladimir N Silnikov; Michael K Bowman; Elena G Bagryanskaya; Tatyana S Godovikova
Journal:  RSC Med Chem       Date:  2020-04-02

2.  An intermediate state of the gamma-aminobutyric acid transporter GAT1 revealed by simultaneous voltage clamp and fluorescence.

Authors:  M Li; R A Farley; H A Lester
Journal:  J Gen Physiol       Date:  2000-04       Impact factor: 4.086

  2 in total

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