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Prometabolites of 5‐Diphospho‐myo‐inositol Pentakisphosphate
Authors:Igor Pavlovic  Divyeshsinh T. Thakor  Priv.‐Doz. Dr. Laurent Bigler  Dr. Miranda S. C. Wilson  Debabrata Laha  Dr. Gabriel Schaaf  Prof. Dr. Adolfo Saiardi  Prof. Dr. Henning J. Jessen
Affiliation:1. Department of Chemistry, University of Zürich (UZH), Winterthurerstrasse 190, 8057 Zürich (Switzerland);2. LMCB, University College London (UK);3. Center for Plant Molecular Biology, University of Tübingen (Germany)
Abstract:Diphospho‐myo‐inositol phosphates (PP‐InsPy) are an important class of cellular messengers. Thus far, no method for the transport of PP‐InsPy into living cells is available. Owing to their high negative charge density, PP‐InsPy will not cross the cell membrane. A strategy to circumvent this issue involves the generation of precursors in which the negative charges are masked with biolabile groups. A PP‐InsPy prometabolite would require twelve to thirteen biolabile groups, which need to be cleaved by cellular enzymes to release the parent molecules. Such densely modified prometabolites of phosphate esters and anhydrides have never been reported to date. This study discloses the synthesis of such agents and an analysis of their metabolism in tissue homogenates by gel electrophoresis. The acetoxybenzyl‐protected system is capable of releasing 5‐PP‐InsP5 in mammalian cell/tissue homogenates within a few minutes and can be used to release 5‐PP‐InsP5 inside cells. These molecules will serve as a platform for the development of fundamental tools required to study PP‐InsPy physiology.
Keywords:Inositol pyrophosphates  metabolism  protecting groups  second messengers
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