Litcius/Paper detail

Does Cyclic ADP-Ribose (cADPR) Activate the Non-selective Cation Channel TRPM2?

Ralf Fliegert, Winnie Maria Riekehr, Andreas H. Guse

2020Frontiers in Immunology18 citationsDOIOpen Access PDF

Abstract

TRPM2 is a non-selective, Ca2+-permeable cation channel widely expressed in immune cells. It is firmly established that the channel can be activated by intracellular adenosine 5’-diphosphoribose (ADPR). Until recent cryo-EM structures have exhibited an additional nucleotide binding site in the N-terminus of the channel, this activation was thought to occur via binding to a C-terminal domain of the channel that is highly homologous to the ADPR pyrophosphatase NudT9. Over the years it has been controversially discussed whether the Ca2+ mobilising second messenger cyclic ADP ribose (cADPR) might also directly activate Ca2+ entry via TRPM2. Here we will review the status of this discussion.

Topics & Concepts

TRPM2Cyclic ADP-riboseChemistryBiochemistryRiboseTransient receptor potential channelCell biologyBiophysicsBiologyEnzymeReceptorCD38CD34Stem cellCalcium signaling and nucleotide metabolismIon Channels and ReceptorsPiperaceae Chemical and Biological Studies