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The Stability of N-Ethylmaleimide and its Reaction with Sulfhydryl Groups
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This article is published in Journal of the American Chemical Society.The article was published on 1955-07-01. It has received 336 citations till now.read more
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Effect of Thiol-Binding Reagents on the Metabolism of Thiosulfate and Tetrathionate by Thiobacillus neapolitanus
TL;DR: Three types of thiol group appear to be associated with the metabolism of thiosulfate and tetrathionate; one of these types may be located at the bacterial cell membrane and consistent with the hypothesis that thiols (or disulfide groups) are binding sites for the substrates.
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Purification and Properties of l‐6‐Hydroxynicotine Oxidase
Vo Dang Dai,K. Decker,H. Sund +2 more
TL;DR: l-6-Hydroxynicotine oxidase, an inducible enzyme of nicotine catabolism in Arthrobacter oxidans, was obtained as a homogeneous protein, as judged by electrophoresis and ultracentrifuge studies; it forms hexagonal crystals in ammonium sulfate solution.
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Stabilities of the fluorescent SH-reagent eosin-5-maleimide and its adducts with sulfhydryl compounds.
TL;DR: Kinetic analyses showed that these open-type and thiazine-type adducts were readily formed and were stable at moderately alkaline pH values such as pH 8.0 or 9.0.
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Glucose transport by trypsin-treated red blood cell ghosts
TL;DR: The onset of glucose transport has been correlated with the pattern of cleavage of membrane peptides (assessed by polyacrylamide gel electrophoresis in sodium dodecyl sulfate).
Journal ArticleDOI
Photo-induced radical thiol–ene chemistry: a versatile toolbox for peptide-based drug design
TL;DR: A toolbox of chemical approaches has been explored for peptide modification to overcome these obstacles as mentioned in this paper, and there has been a revival of interest in photoinduced radical thiol-ene chemistry as a powerful tool for the construction of therapeutic peptides.