دورية أكاديمية

A novel image-based high-throughput screening assay discovers therapeutic candidates for adult polyglucosan body disease

التفاصيل البيبلوغرافية
العنوان: A novel image-based high-throughput screening assay discovers therapeutic candidates for adult polyglucosan body disease
المؤلفون: Solmesky, Leonardo J., Khazanov, Netaly, Senderowitz, Hanoch, Wang, Peixiang, Minassian, Berge A., Ferreira, Igor M., Yue, Wyatt W., Lossos, Alexander, Weil, Miguel, Kakhlon, Or
المصدر: Biochemical Journal ; volume 474, issue 20, page 3403-3420 ; ISSN 0264-6021 1470-8728
بيانات النشر: Portland Press Ltd.
سنة النشر: 2017
مصطلحات موضوعية: Cell Biology, Molecular Biology, Biochemistry
الوصف: Glycogen storage disorders (GSDs) are caused by excessive accumulation of glycogen. Some GSDs [adult polyglucosan (PG) body disease (APBD), and Tarui and Lafora diseases] are caused by intracellular accumulation of insoluble inclusions, called PG bodies (PBs), which are chiefly composed of malconstructed glycogen. We developed an APBD patient skin fibroblast cell-based assay for PB identification, where the bodies are identified as amylase-resistant periodic acid–Schiff's-stained structures, and quantified. We screened the DIVERSet CL 10 084 compound library using this assay in high-throughput format and discovered 11 dose-dependent and 8 non-dose-dependent PB-reducing hits. Approximately 70% of the hits appear to act through reducing glycogen synthase (GS) activity, which can elongate glycogen chains and presumably promote PB generation. Some of these GS inhibiting hits were also computationally predicted to be similar to drugs interacting with the GS activator protein phosphatase 1. Our work paves the way to discovering medications for the treatment of PB-involving GSD, which are extremely severe or fatal disorders.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1042/bcj20170469
الإتاحة: https://doi.org/10.1042/bcj20170469Test
https://portlandpress.com/biochemj/article-pdf/474/20/3403/691311/bcj-2017-0469.pdfTest
رقم الانضمام: edsbas.BF646C0D
قاعدة البيانات: BASE