Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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Materials Map under construction

The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2016Dynamic association of calcium channel subunits at the cellular membrane.25citations

Places of action

Chart of shared publication
Voigt, A.
1 / 6 shared
Thomas, U.
1 / 1 shared
Missler, Markus
1 / 2 shared
Freund, R.
1 / 1 shared
Heck, Jennifer
1 / 1 shared
Heine, Martin
1 / 2 shared
Chart of publication period
2016

Co-Authors (by relevance)

  • Voigt, A.
  • Thomas, U.
  • Missler, Markus
  • Freund, R.
  • Heck, Jennifer
  • Heine, Martin
OrganizationsLocationPeople

article

Dynamic association of calcium channel subunits at the cellular membrane.

  • Voigt, A.
  • Thomas, U.
  • Missler, Markus
  • Freund, R.
  • Obermair, Gerald
  • Heck, Jennifer
  • Heine, Martin
Abstract

High voltage gated calcium channels (VGCCs) are composed of at least three subunits, one pore forming [Formula: see text]-subunit, an intracellular [Formula: see text]-variant, and a mostly extracellular [Formula: see text]-variant. Interactions between these subunits determine the kinetic properties of VGCCs. It is unclear whether these interactions are stable over time or rather transient. Here, we used single-molecule tracking to investigate the surface diffusion of [Formula: see text]- and [Formula: see text]-subunits at the cell surface. We found that [Formula: see text]-subunits show higher surface mobility than [Formula: see text]-subunits, and that they are only transiently confined together, suggesting a weak association between [Formula: see text]- and [Formula: see text]-subunits. Moreover, we observed that different [Formula: see text]-subunits engage in different degrees of association with the [Formula: see text]-subunit, revealing the tighter interaction of [Formula: see text] with [Formula: see text]. These data indicate a distinct regulation of the [Formula: see text] interaction in VGCC subtypes. We modeled their membrane dynamics in a Monte Carlo simulation using experimentally determined diffusion constants. Our modeling predicts that the ratio of associated [Formula: see text]- and [Formula: see text]-subunits mainly depends on their expression density and confinement in the membrane. Based on the different motilities of particular [Formula: see text]-subunit combinations, we propose that their dynamic assembly and disassembly represent an important mechanism to regulate the signaling properties of VGCC.

Topics
  • density
  • impedance spectroscopy
  • pore
  • surface
  • mobility
  • simulation
  • forming
  • Calcium