The facile synthesis of serine, threonine, and cysteine β-glycosides using commercially available peracetylated β- N-acetylglucosamine (β-AcGlcNAc) and catalytic amounts of indium bromide (InBr) is described. This method involves only inexpensive reagents that require no further modification or special handling. The reagents are simply mixed, dissolved, and refluxed to afford the GlcNAcylated amino acids in great yields (70-80%). This operationally simple procedure should facilitate the study of O-GlcNAcylation without necessitating expertise in synthetic carbohydrate chemistry.
The
nuclear receptor-related 1 protein, Nurr1, is a transcription
factor critical for the development and maintenance of dopamine-producing
neurons in the substantia nigra pars compacta, a cell population that
progressively loses the ability to make dopamine and degenerates in
Parkinson’s disease. Recently, we demonstrated that Nurr1 binds
directly to and is regulated by the endogenous dopamine metabolite
5,6-dihydroxyindole (DHI). Unfortunately, DHI is an unstable compound,
and thus a poor tool for studying Nurr1 function. Here, we report
that 5-chloroindole, an unreactive analog of DHI, binds directly to
the Nurr1 ligand binding domain with micromolar affinity and stimulates
the activity of Nurr1, including the transcription of genes governing
the synthesis and packaging of dopamine.
The nuclear receptor-related protein, Nurr1, is a transcription factor critical for the development and maintenance of dopamine-producing neurons in the substantia nigra pars compacta, a cell population that progressively loses the ability to make dopamine and degenerates in Parkinson's disease. Recently, we demonstrated that Nurr1 binds directly to and is regulated by the endogenous dopamine metabolite 5,6-dihydroxyindole (DHI). Unfortunately, DHI is an unstable compound, and thus a poor tool for studying Nurr1 function. Here we report that 5-chloroindoe, an unreactive analog of DHI, binds directly to the Nurr1 ligand binding domain with micromolar affinity and stimulates the activity of Nurr1, including the transcription of genes governing the synthesis and packaging of dopamine.
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