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An Improved Two-Dimensional HPLC Method for Endogenous 2'-Deoxy-ADPR and 2'-Deoxy-NAD
Feng Gu1, Ralf Fliegert1, Andreas Bauche1
1The Calcium Signaling Group, Department of Biochemistry and Molecular Cell Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Abstract:
Transient receptor potential melastatin 2 (TRPM2) is a multifunctional non-selective Ca2+-permeable cation channel expressed in numerous immune cells. 2'-Deoxy-adenosine diphosphoribose (2d-ADPR) has been identified as a superagonist of TRPM2 channels that induces higher whole-cell currents and requires a lower intracellular Ca2+ concentration for activation. 2d-ADPR can be produced from 2'-deoxy-nicotinamide adenine dinucleotide (2d-NAD) by the enzyme CD38 in vitro under physiological conditions.Here, we describe a two-dimensional HPLC method, suitable for the quantification of endogenous 2d-ADPR and 2d-NAD. The results demonstrated that 25 million Jurkat T cells per sample were sufficient to quantify endogenous 2d-ADPR and 2d-NAD.
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