Vitya Vardanyan

Vitya Vardanyan
Institute of Molecular Biology, National Academy of Sciences of Armenia · Molecular Neuroscience

PhD

About

16
Publications
1,733
Reads
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727
Citations
Citations since 2017
1 Research Item
262 Citations
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2017201820192020202120222023010203040
2017201820192020202120222023010203040
2017201820192020202120222023010203040
Additional affiliations
January 2012 - present
National Academy of Sciences of Armenia
Position
  • Principal Investigator
Description
  • Subject: KCNQ potassium channels: structure, function, physiology and pathology
October 2007 - October 2012
Zentrum für Molekulare Neurobiologie Hamburg
Position
  • Leader of electrophysiology subgroup
Description
  • Subject: Gating mechanisms of voltage-dependent potassium channels.
October 2007 - October 2011
Zentrum für Molekulare Neurobiologie Hamburg
Position
  • CO-SUPERVISION OF THESES
Description
  • 1. Co-supervised the PhD thesis “Inactivation gating of potassium channels” of Phanindra Velisetty. 2. Co-supervising the PhD thesis “Structural and functional investigation of KcsA potassium channel in different lipid environment” of Alexander Prokofyev.
Education
October 1999 - September 2003
September 1995 - August 1998
September 1990 - August 1995
Yerevan State University
Field of study
  • Biophysics

Publications

Publications (16)
Article
Full-text available
MiDCA1, a phospholipase A 2 (PLA 2 ) neurotoxin isolated from Micrurus dumerilii carinicauda coral snake venom, inhibited a major component of voltage-activated potassium (Kv) currents (41 ± 3% inhibition with 1 μM toxin) in mouse cultured dorsal root ganglion (DRG) neurons. In addition, the selective Kv2.1 channel blocker guangxitoxin (GxTx-1E) an...
Article
Full-text available
The activation of voltage-dependent ion channels is initiated by potential-induced conformational rearrangements in the voltage-sensor domains that propagates to the pore domain (PD) and finally opens the ion conduction pathway. In potassium channels voltage-sensors are covalently linked to the pore via S4-S5 linkers at the cytoplasmic site of the...
Article
Full-text available
Mutations inactivating the potassium channel KCNQ4 (K(v)7.4) lead to deafness in humans and mice. In addition to its expression in mechanosensitive hair cells of the inner ear, KCNQ4 is found in the auditory pathway and in trigeminal nuclei that convey somatosensory information. We have now detected KCNQ4 in the peripheral nerve endings of cutaneou...
Article
Full-text available
Controlled opening and closing of an ion-selective pathway in response to changes of membrane potential is a fundamental feature of voltage-gated ion channels. In recent decades, various details of this process have been revealed with unprecedented precision based on studies of prototypic potassium channels. Though current scientific efforts are fo...
Article
The response of voltage-dependent K+ (Kv) channels to a change in membrane voltage involves a molecular device, which couples voltage-driven conformational changes to gate opening and closing within the channel's conduction pathway. To further our understanding of the coupling choreography we have studied how changes in coupling strength instigate...
Article
Full-text available
Potassium (K(+))-channel gating is choreographed by a complex interplay between external stimuli, K(+) concentration and lipidic environment. We combined solid-state NMR and electrophysiological experiments on a chimeric KcsA-Kv1.3 channel to delineate K(+), pH and blocker effects on channel structure and function in a membrane setting. Our data sh...
Article
Full-text available
KCNQ4 is an M-type K+ channel expressed in sensory hair cells of the inner ear and in the central auditory pathway. KCNQ4 mutations underlie human DFNA2 dominant progressive hearing loss. We now generated mice in which the KCNQ4 gene was disrupted or carried a dominant negative DFNA2 mutation. Although KCNQ4 is strongly expressed in vestibular hair...
Article
We have found a novel nonsense mutation in the C-terminus of HERG in a four-generation Chinese family with long QT syndrome and investigated the molecular mechanism of this mutation in vitro. Six family members, including the proband, were clinically affected. Syncope and ventricular tachycardia of torsades de pointes were triggered by startling or...
Article
The effect of Kvbeta3 subunit co-expression on currents mediated by the Shaker-related channels Kv1.1 to Kv1.6 in Chinese hamster ovary (CHO) cells was studied with patch-clamp techniques. In the presence of Kvbeta3, differences in the voltage dependence of activation for Kv1.1, Kv1.3 and Kv1.6 were detected, but not for Kv1.2- and Kv1.4-mediated c...
Article
To identify the underlying genetic basis of a Chinese pedigree with Long QT syndrome, the causally related genes were screened in a family and the functional consequence of the identified gene mutation was evaluated in vitro. Mutations in the five defined Long QT syndrome related genes were screened with polymerase chain reaction and single-strand...
Article
The KCNE genes encode small, single transmembrane domain peptides that associate with pore-forming potassium channel subunits to form mixed complexes with unique characteristics. We have identified a novel member of the human KCNE gene family, hKCNE4. The hKCNE4 gene encodes 170 amino acid protein and is localized to chromosome 2q35-36. The protein...
Article
Full-text available
The accessory beta subunits of voltage-dependent potassium (Kv) channels form tetramers arranged with 4-fold rotational symmetry like the membrane-integral and pore-forming alpha subunits (Gulbis, J. M., Mann, S., and MacKinnon, R. (1999) Cell. 90, 943-952). The crystal structure of the Kvbeta2 subunit shows that Kvbeta subunits are oxidoreductase...
Article
K+ uptake by the Escherichia coli TrkA system is unusual in that it requires both ATP and deltamuH+; a relation with H+ circulation through the membrane is therefore suggested. The relationship of this system with the F0F1-ATPase was studied in intact cells grown under different conditions. A significant increase of the N,N'-dicyclohexylcarbodiimid...

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