Literature DB >> 9119064

Synaptotagmin restores kinetic properties of a syntaxin-associated N-type voltage sensitive calcium channel.

O Wiser1, D Tobi, M Trus, D Atlas.   

Abstract

The voltage sensitive N-type calcium channel interacts functionally and biochemically with synaptotagmin (p65). N-type channel interaction with p65 is demonstrated in the Xenopus oocyte expression system, where p65 alters the steady state voltage inactivation of the N-channel, and fully restores the syntaxin-modified current amplitude and inactivation kinetics in a calcium dependent manner. In agreement with the functional results, GST-p65 fusion protein binds to a cytosolic region, amino acids 710-1090 of the N-type channel (N-loop(710-1090)). The results of the combined approach provide a functional and biochemical basis for proposing that p65 interaction with the N-type channel brings p65 into a close association with a syntaxin-coupled channel. In turn, calcium entry through the liberated channel initiates fusion of the primed vesicles with the cell membrane at a short distance from the site of calcium entry.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9119064     DOI: 10.1016/s0014-5793(97)00130-0

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  24 in total

Review 1.  Localized calcium influx in pancreatic beta-cells: its significance for Ca2+-dependent insulin secretion from the islets of Langerhans.

Authors:  L S Satin
Journal:  Endocrine       Date:  2000-12       Impact factor: 3.633

Review 2.  Interactions between proteins implicated in exocytosis and voltage-gated calcium channels.

Authors:  M Seagar; C Lévêque; N Charvin; B Marquèze; N Martin-Moutot; J A Boudier; J L Boudier; Y Shoji-Kasai; K Sato; M Takahashi
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1999-02-28       Impact factor: 6.237

3.  Molecular determinants of the functional interaction between syntaxin and N-type Ca2+ channel gating.

Authors:  I Bezprozvanny; P Zhong; R H Scheller; R W Tsien
Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-05       Impact factor: 11.205

4.  Enhancement of presynaptic calcium current by cysteine string protein.

Authors:  Shan Chen; Xu Zheng; Karen L Schulze; Terry Morris; Hugo Bellen; Elis F Stanley
Journal:  J Physiol       Date:  2002-01-15       Impact factor: 5.182

5.  Direct measurement of single-channel Ca(2+) currents in bullfrog hair cells reveals two distinct channel subtypes.

Authors:  A Rodriguez-Contreras; E N Yamoah
Journal:  J Physiol       Date:  2001-08-01       Impact factor: 5.182

6.  A Ca(v)3.2/syntaxin-1A signaling complex controls T-type channel activity and low-threshold exocytosis.

Authors:  Norbert Weiss; Shahid Hameed; José M Fernández-Fernández; Katell Fablet; Maria Karmazinova; Cathy Poillot; Juliane Proft; Lina Chen; Isabelle Bidaud; Arnaud Monteil; Sylvaine Huc-Brandt; Lubica Lacinova; Philippe Lory; Gerald W Zamponi; Michel De Waard
Journal:  J Biol Chem       Date:  2011-11-30       Impact factor: 5.157

7.  Molecular identification and reconstitution of depolarization-induced exocytosis monitored by membrane capacitance.

Authors:  Roy Cohen; Bernhard M Schmitt; Daphne Atlas
Journal:  Biophys J       Date:  2005-09-08       Impact factor: 4.033

Review 8.  Interactions between presynaptic calcium channels and proteins implicated in synaptic vesicle trafficking and exocytosis.

Authors:  M Seagar; M Takahashi
Journal:  J Bioenerg Biomembr       Date:  1998-08       Impact factor: 2.945

9.  Conformational changes induced in voltage-gated calcium channel Cav1.2 by BayK 8644 or FPL64176 modify the kinetics of secretion independently of Ca2+ influx.

Authors:  Merav Marom; Yamit Hagalili; Ariel Sebag; Lior Tzvier; Daphne Atlas
Journal:  J Biol Chem       Date:  2010-01-06       Impact factor: 5.157

Review 10.  Regulation of Ca(V)2 calcium channels by G protein coupled receptors.

Authors:  Gerald W Zamponi; Kevin P M Currie
Journal:  Biochim Biophys Acta       Date:  2012-10-12
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.