Universität zu Köln

Neurnaier, Felix, Dibue-Adjei, Maxine, Hescheler, Juergen and Schneider, Toni (2015). Voltage-gated calcium channels: Determinants of channel function and modulation by inorganic cations. Prog. Neurobiol., 129. S. 1 - 37. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 1873-5118

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Abstract

Voltage-gated calcium channels (VGCCs) represent a key link between electrical signals and non-electrical processes, such as contraction, secretion and transcription. Evolved to achieve high rates of Cu2+-selective flux, they possess an elaborate mechanism for selection of Cu2+ over foreign ions. It has been convincingly linked to competitive binding in the pore, but the fundamental question of how this is reconcilable with high rates of Cu2+ transfer remains unanswered. By virtue of their similarity to Cu2+, polyvalent cations can interfere with the function of VGCCs and have proven instrumental in probing the mechanisms underlying selective permeation. Recent emergence of crystallographic data on a set of Cu2+-selective model channels provides a structural framework for permeation in VGCCs, and warrants a reconsideration of their diverse modulation by polyvalent cations, which can be roughly separated into three general mechanisms: (I) long-range interactions with charged regions on the surface, affecting the local potential sensed by the channel or influencing voltage-sensor movement by repulsive forces (electrostatic effects), (II) short-range interactions with sites in the ion-conducting pathway, leading to physical obstruction of the channel (pore block), and in some cases (III) short-range interactions with extracellular binding sites, leading to non-electrostatic modifications of channel gating (allosteric effects). These effects, together with the underlying molecular modifications, provide valuable insights into the function of VGCCs, and have important physiological and pathophysiological implications. Allosteric suppression of some of the pore-forming Ca-v alpha(1)-subunits (Ca(v)2.3, Ca(v)3.2) by Zn2+ and Cu2+ may play a major role for the regulation of excitability by endogenous transition metal ions. The fact that these ions can often traverse VGCCs can contribute to the detrimental intracellular accumulation of metal ions following excessive release of endogenous Cu2+ and Zn2+ or exposure to non-physiological toxic metal ions. (C) 2015 Elsevier Ltd. All rights reserved.

Item Type:	Journal Article
Creators:	Creators Email ORCID ORCID Put Code Neurnaier, Felix UNSPECIFIED UNSPECIFIED UNSPECIFIED Dibue-Adjei, Maxine UNSPECIFIED UNSPECIFIED UNSPECIFIED Hescheler, Juergen UNSPECIFIED UNSPECIFIED UNSPECIFIED Schneider, Toni UNSPECIFIED UNSPECIFIED UNSPECIFIED
URN:	urn:nbn:de:hbz:38-402561
DOI:	10.1016/j.pneurobio.2014.12.003
Journal or Publication Title:	Prog. Neurobiol.
Volume:	129
Page Range:	S. 1 - 37
Date:	2015
Publisher:	PERGAMON-ELSEVIER SCIENCE LTD
Place of Publication:	OXFORD
ISSN:	1873-5118
Language:	English
Faculty:	Unspecified
Divisions:	Unspecified
Subjects:	no entry
Uncontrolled Keywords:	Keywords Language HIPPOCAMPAL PYRAMIDAL NEURONS; DEPENDENT ACTION-POTENTIALS; AFFINITY ZINC INHIBITION; NEGATIVE SURFACE-CHARGE; CENTRAL-NERVOUS-SYSTEM; GUINEA-PIG MYOCARDIUM; CHICK SENSORY NEURONS; MONO-VALENT CATIONS; SMOOTH-MUSCLE CELLS; SLOW INWARD CURRENT Multiple languages Neurosciences Multiple languages
URI:	http://kups.ub.uni-koeln.de/id/eprint/40256