Elucidating Diphosphoinositol Polyphosphate Function with Nonhydrolyzable Analogues1. (30th May 2014)

• Record Type: Journal Article
• Authors: Wu, Mingxuan; Chong, Lucy S.; Capolicchio, Samanta; Jessen, Henning J.; Resnick, Adam C.; Fiedler, Dorothea
• Is Part Of: Angewandte Chemie. Volume 126:Number 28(2014)
• Page Start: 7320
• Page End: 7325
• Publication Date: 2014-05-30
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.201402905
• Languages: English
• ISSNs: 0044-8249

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The diphosphoinositol polyphosphates (PP‐IPs) represent a novel class of high‐energy phosphate‐containing messengers which control a wide variety of cellular processes. It is thought that PP‐IPs exert their pleiotropic effects as allosteric regulators and through pyrophosphorylation of protein substrates. However, most details of PP‐IP signaling have remained elusive because of a paucity of suitable tools. We describe the synthesis of PP‐IP bisphosphonate analogues (PCP‐IPs), which are resistant to chemical and biochemical degradation. While the two regioisomers 1PCP‐IP₅ and 5PCP‐IP₅ inhibited Akt phosphorylation with similar potencies, 1PCP‐IP₅ was much more effective at inhibiting its cognate phosphatase hDIPP1. Furthermore, the PCP analogues inhibit protein pyrophosphorylation because of their inability to transfer the β‐phosphoryl group, and thus enable the distinction between PP‐IP signaling mechanisms. As such, the PCP analogues will find widespread applications for the structural and biochemical characterization of PP‐IP signaling properties.</p> </abstract>