The E1015K variant in the synprint region of the CaV2.1 channel alters channel function and is associated with different migraine phenotypes

Steven B. Condliffe, Alessandra Fratangeli, Nehan R. Munasinghe, Elena Saba, Maria Passafaro, Cristina Montrasio, Maurizio Ferrari, Patrizia Rosa, Paola Carrera

Research output: Contribution to journalArticle

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Abstract

Mutations in the CACNA1A gene, which encodes the poreforming α1A subunit of the CaV2.1 voltage-gated calcium channel, cause a number of human neurologic diseases including familial hemiplegic migraine. We have analyzed the functional impact of the E1015K amino acid substitution located in the "synprint" domain of the α1A subunit. This variant was identified in two families with hemiplegic migraine and in one patient with migraine with aura. The wild type (WT) and the E1015K forms of the GFP-tagged α1A subunit were expressed in cultured hippocampal neurons and HEK cells to understand the role of the variant in the transport activity and physiology of CaV2.1. The E1015K variant does not alter CaV2.1 protein expression, and its transport to the cell surface and synaptic terminals is similar to that observed for WT channels. Electrophysiological data demonstrated that E1015K channels have increased current density and significantly altered inactivation properties compared with WT. Furthermore, the SNARE proteins syntaxin 1A and SNAP-25 were unable to modulate voltage-dependent inactivation of E1015K channels. Overall, our findings describe a genetic variant in the synprint site of the CaV2.1 channel which is characterized by a gain-of-function and associated with both hemiplegic migraine and migraine with aura in patients.

Original languageEnglish
Pages (from-to)33873-33883
Number of pages11
JournalJournal of Biological Chemistry
Volume288
Issue number47
DOIs
Publication statusPublished - Nov 22 2013

Fingerprint

Migraine Disorders
Migraine with Aura
Phenotype
Syntaxin 1
SNARE Proteins
Physiology
Presynaptic Terminals
Electric potential
Amino Acid Substitution
Calcium Channels
Nervous System Diseases
Neurons
Substitution reactions
Current density
Genes
Amino Acids
Mutation
voltage-dependent calcium channel (P-Q type)
Proteins

ASJC Scopus subject areas

  • Biochemistry
  • Cell Biology
  • Molecular Biology

Cite this

The E1015K variant in the synprint region of the CaV2.1 channel alters channel function and is associated with different migraine phenotypes. / Condliffe, Steven B.; Fratangeli, Alessandra; Munasinghe, Nehan R.; Saba, Elena; Passafaro, Maria; Montrasio, Cristina; Ferrari, Maurizio; Rosa, Patrizia; Carrera, Paola.

In: Journal of Biological Chemistry, Vol. 288, No. 47, 22.11.2013, p. 33873-33883.

Research output: Contribution to journalArticle

Condliffe, Steven B. ; Fratangeli, Alessandra ; Munasinghe, Nehan R. ; Saba, Elena ; Passafaro, Maria ; Montrasio, Cristina ; Ferrari, Maurizio ; Rosa, Patrizia ; Carrera, Paola. / The E1015K variant in the synprint region of the CaV2.1 channel alters channel function and is associated with different migraine phenotypes. In: Journal of Biological Chemistry. 2013 ; Vol. 288, No. 47. pp. 33873-33883.
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