Literature DB >> 15339810

Negatively charged residues in the N-terminal of the AID helix confer slow voltage dependent inactivation gating to CaV1.2.

Omar Dafi1, Laurent Berrou, Yolaine Dodier, Alexandra Raybaud, Rémy Sauvé, Lucie Parent.   

Abstract

The E462R mutation in the fifth position of the AID (alpha1 subunit interaction domain) region in the I-II linker is known to significantly accelerate voltage-dependent inactivation (VDI) kinetics of the L-type CaV1.2 channel, suggesting that the AID region could participate in a hinged-lid type inactivation mechanism in these channels. The recently solved crystal structures of the AID-CaVbeta regions in L-type CaV1.1 and CaV1.2 channels have shown that in addition to E462, positions occupied by Q458, Q459, E461, K465, L468, D469, and T472 in the rabbit CaV1.2 channel could also potentially contribute to a hinged-lid type mechanism. A mutational analysis of these residues shows that Q458A, Q459A, K465N, L468R, D469A, and T472D did not significantly alter VDI gating. In contrast, mutations of the negatively charged E461, E462, and D463 to neutral or positively charged residues increased VDI gating, suggesting that the cluster of negatively charged residues in the N-terminal end of the AID helix could account for the slower VDI kinetics of CaV1.2. A mutational analysis at position 462 (R, K, A, G, D, N, Q) further confirmed that E462R yielded faster VDI kinetics at +10 mV than any other residue with E462R >> E462K approximately E462A > E462N > wild-type approximately E462Q approximately E462G > E462D (from the fastest to the slowest). E462R was also found to increase the VDI gating of the slow CEEE chimera that includes the I-II linker from CaV1.2 into a CaV2.3 background. The fast VDI kinetics of the CaV1.2 E462R and the CEEE + E462R mutants were abolished by the CaVbeta2a subunit and reinstated when using the nonpalmitoylated form of CaVbeta2a C3S + C4S (CaVbeta2a CS), confirming that CaVbeta2a and E462R modulate VDI through a common pathway, albeit in opposite directions. Altogether, these results highlight the unique role of E461, E462, and D463 in the I-II linker in the VDI gating of high-voltage activated CaV1.2 channels.

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Year:  2004        PMID: 15339810      PMCID: PMC1304788          DOI: 10.1529/biophysj.104.045559

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  49 in total

1.  Molecular determinants of inactivation within the I-II linker of alpha1E (CaV2.3) calcium channels.

Authors:  L Berrou; G Bernatchez; L Parent
Journal:  Biophys J       Date:  2001-01       Impact factor: 4.033

2.  Fast inactivation of voltage-dependent calcium channels. A hinged-lid mechanism?

Authors:  S C Stotz; J Hamid; R L Spaetgens; S E Jarvis; G W Zamponi
Journal:  J Biol Chem       Date:  2000-08-11       Impact factor: 5.157

3.  Role of Repeat I in the fast inactivation kinetics of the Ca(V)2.3 channel.

Authors:  G Bernatchez; L Berrou; Z Benakezouh; J Ducay; L Parent
Journal:  Biochim Biophys Acta       Date:  2001-10-01

4.  Molecular determinants of voltage-dependent slow inactivation of the Ca2+ channel.

Authors:  Chengzhang Shi; Nikolai M Soldatov
Journal:  J Biol Chem       Date:  2001-12-18       Impact factor: 5.157

5.  The role of region IVS5 of the human cardiac calcium channel in establishing inactivated channel conformation: use-dependent block by benzothiazepines.

Authors:  Ilona Bodi; Sheryl E Koch; Hiroshi Yamaguchi; Gyula P Szigeti; Arnold Schwartz; Gyula Varadi
Journal:  J Biol Chem       Date:  2002-03-23       Impact factor: 5.157

6.  Identification of inactivation determinants in the domain IIS6 region of high voltage-activated calcium channels.

Authors:  S C Stotz; G W Zamponi
Journal:  J Biol Chem       Date:  2001-06-11       Impact factor: 5.157

7.  Potassium channel receptor site for the inactivation gate and quaternary amine inhibitors.

Authors:  M Zhou; J H Morais-Cabral; S Mann; R MacKinnon
Journal:  Nature       Date:  2001-06-07       Impact factor: 49.962

8.  Ca2+/calmodulin binds to and modulates P/Q-type calcium channels.

Authors:  A Lee; S T Wong; D Gallagher; B Li; D R Storm; T Scheuer; W A Catterall
Journal:  Nature       Date:  1999-05-13       Impact factor: 49.962

9.  State-dependent inhibition of inactivation-deficient Ca(V)1.2 and Ca(V)2.3 channels by mibefradil.

Authors:  G Bernatchez; R Sauvé; L Parent
Journal:  J Membr Biol       Date:  2001-11-15       Impact factor: 1.843

10.  Voltage-dependent acceleration of Ca(v)1.2 channel current decay by (+)- and (-)-isradipine.

Authors:  S Berjukow; S Hering
Journal:  Br J Pharmacol       Date:  2001-08       Impact factor: 8.739

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  10 in total

1.  Kinetic properties of the cardiac L-type Ca2+ channel and its role in myocyte electrophysiology: a theoretical investigation.

Authors:  Gregory M Faber; Jonathan Silva; Leonid Livshitz; Yoram Rudy
Journal:  Biophys J       Date:  2006-12-08       Impact factor: 4.033

2.  Calmodulin mutations associated with long QT syndrome prevent inactivation of cardiac L-type Ca(2+) currents and promote proarrhythmic behavior in ventricular myocytes.

Authors:  Worawan B Limpitikul; Ivy E Dick; Rosy Joshi-Mukherjee; Michael T Overgaard; Alfred L George; David T Yue
Journal:  J Mol Cell Cardiol       Date:  2014-05-08       Impact factor: 5.000

3.  Molecular endpoints of Ca2+/calmodulin- and voltage-dependent inactivation of Ca(v)1.3 channels.

Authors:  Michael R Tadross; Manu Ben Johny; David T Yue
Journal:  J Gen Physiol       Date:  2010-02-08       Impact factor: 4.086

4.  Ca2+-binding protein 2 inhibits Ca2+-channel inactivation in mouse inner hair cells.

Authors:  Maria Magdalena Picher; Anna Gehrt; Sandra Meese; Aleksandra Ivanovic; Friederike Predoehl; SangYong Jung; Isabelle Schrauwen; Alberto Giulio Dragonetti; Roberto Colombo; Guy Van Camp; Nicola Strenzke; Tobias Moser
Journal:  Proc Natl Acad Sci U S A       Date:  2017-02-09       Impact factor: 11.205

5.  Alanine-scanning mutagenesis defines a conserved energetic hotspot in the CaValpha1 AID-CaVbeta interaction site that is critical for channel modulation.

Authors:  Filip Van Petegem; Karl E Duderstadt; Kimberly A Clark; Michelle Wang; Daniel L Minor
Journal:  Structure       Date:  2008-02       Impact factor: 5.006

6.  Roscovitine, a cyclin-dependent kinase inhibitor, affects several gating mechanisms to inhibit cardiac L-type (Ca(V)1.2) calcium channels.

Authors:  V Yarotskyy; K S Elmslie
Journal:  Br J Pharmacol       Date:  2007-08-13       Impact factor: 8.739

7.  Mutations of nonconserved residues within the calcium channel alpha1-interaction domain inhibit beta-subunit potentiation.

Authors:  Giovanni Gonzalez-Gutierrez; Erick Miranda-Laferte; David Naranjo; Patricia Hidalgo; Alan Neely
Journal:  J Gen Physiol       Date:  2008-09       Impact factor: 4.086

8.  A bilobal model of Ca2+-dependent inactivation to probe the physiology of L-type Ca2+ channels.

Authors:  Worawan B Limpitikul; Joseph L Greenstein; David T Yue; Ivy E Dick; Raimond L Winslow
Journal:  J Gen Physiol       Date:  2018-11-23       Impact factor: 4.086

9.  Disruption of the IS6-AID linker affects voltage-gated calcium channel inactivation and facilitation.

Authors:  Felix Findeisen; Daniel L Minor
Journal:  J Gen Physiol       Date:  2009-03       Impact factor: 4.086

10.  An autism-associated mutation in CaV1.3 channels has opposing effects on voltage- and Ca(2+)-dependent regulation.

Authors:  Worawan B Limpitikul; Ivy E Dick; Manu Ben-Johny; David T Yue
Journal:  Sci Rep       Date:  2016-06-03       Impact factor: 4.379

  10 in total

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