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Sites and Regulation of L-Type Ca2+ Channel Cav1.2 Phosphorylation in Brain

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)

Abstract

Cav1.2 channel phosphorylation plays an important role in regulating neuronal plasticity by action potential-dependent Ca2+ entry. Most studies of Cav1.2 regulation by phosphorylation have been reported in heart and muscles. Here, we identified phosphorylation sites of neuronal Cav1.2 channel protein purified from rat brain using mass spectrometry. The functional characterization of these phosphorylation sites showed altered voltage-dependent biophysical properties of the channel, without affecting current density. These results show that neuronal Cav1.2 channel is regulated by phosphorylation in a complex mechanism involving multiple phosphorylation sites.

Original languageEnglish
Pages (from-to)2427-2431
Number of pages5
JournalCellular and Molecular Neurobiology
Volume42
Issue number7
DOIs
Publication statusPublished - Oct 2022

Bibliographical note

Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Keywords

  • Cav1.2
  • Mass spectrometry
  • Neuron
  • Phosphorylation

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