Literature DB >> 12586831

Maurocalcine and peptide A stabilize distinct subconductance states of ryanodine receptor type 1, revealing a proportional gating mechanism.

Lili Chen1, Eric Estève, Jean-Marc Sabatier, Michel Ronjat, Michel De Waard, Paul D Allen, Isaac N Pessah.   

Abstract

Maurocalcine (MCa) isolated from Scorpio maurus palmatus venom shares 82% sequence identity with imperatoxin A. Both scorpion toxins are putative mimics of the II-III loop peptide (termed peptide A (pA)) of alpha(1s)-dihydropyridine receptor and are thought to act at a common site on ryanodine receptor type 1 (RyR1) important for skeletal muscle EC coupling. The relationship between the actions of synthetic MCa (sMCa) and pA on RyR1 were examined. sMCa released Ca(2+) from SR vesicles (EC(50) = 17.5 nm) in a manner inhibited by micromolar ryanodine or ruthenium red. pA (0.5-40 microm) failed to induce SR Ca(2+) release. Rather, pA enhanced Ca(2+) loading into SR and fully inhibited Ca(2+)-, caffeine-, and sMCa-induced Ca(2+) release. The two peptides modified single channel gating behavior in distinct ways. With Cs(+)-carrying current, 10 nm to 1 microm sMCa induced long lived subconductances having 48% of the characteristic full open state and occasional transitions to 29% at either positive or negative holding potentials. In contrast, pA stabilized long lived channel closures with occasional burst transitions to 65% (s1) and 86% (s2) of the full conductance. The actions of pA and sMCa were observed in tandem. sMCa stabilized additional subconductance states proportional to pA-induced subconductances (i.e. 43% of pA-modified s1 and s2 substates), revealing a proportional gating mechanism. [(3)H]Ryanodine binding and surface plasmon resonance analyses indicated that the peptides did not interact by simple competition for a single class of mutually exclusive sites on RyR1 to produce proportional gating. The actions of sMCa were also observed with ryanodine-modified channels and channels deficient in immunophilin 12-kDa FK506-binding protein. These results provide evidence that sMCa and pA stabilize distinct RyR1 channel states through distinct mechanisms that allosterically stabilize gating states having proportional conductance.

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Year:  2003        PMID: 12586831     DOI: 10.1074/jbc.M209501200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  23 in total

1.  Peptide fragments of the dihydropyridine receptor can modulate cardiac ryanodine receptor channel activity and sarcoplasmic reticulum Ca2+ release.

Authors:  Angela F Dulhunty; Suzanne M Curtis; Louise Cengia; Magdalena Sakowska; Marco G Casarotto
Journal:  Biochem J       Date:  2004-04-01       Impact factor: 3.857

2.  Molecular basis of the high-affinity activation of type 1 ryanodine receptors by imperatoxin A.

Authors:  Chul Won Lee; Eun Hui Lee; Koh Takeuchi; Hideo Takahashi; Ichio Shimada; Kazuki Sato; Song Yub Shin; Do Han Kim; Jae Il Kim
Journal:  Biochem J       Date:  2004-01-15       Impact factor: 3.857

3.  Small efficient cell-penetrating peptides derived from scorpion toxin maurocalcine.

Authors:  Cathy Poillot; Hicham Bichraoui; Céline Tisseyre; Eloi Bahemberae; Nicolas Andreotti; Jean-Marc Sabatier; Michel Ronjat; Michel De Waard
Journal:  J Biol Chem       Date:  2012-03-20       Impact factor: 5.157

4.  Transduction of the scorpion toxin maurocalcine into cells. Evidence that the toxin crosses the plasma membrane.

Authors:  Eric Estève; Kamel Mabrouk; Alain Dupuis; Sophia Smida-Rezgui; Xavier Altafaj; Didier Grunwald; Jean-Claude Platel; Nicolas Andreotti; Isabelle Marty; Jean-Marc Sabatier; Michel Ronjat; Michel De Waard
Journal:  J Biol Chem       Date:  2005-01-14       Impact factor: 5.157

5.  Maurocalcine and domain A of the II-III loop of the dihydropyridine receptor Cav 1.1 subunit share common binding sites on the skeletal ryanodine receptor.

Authors:  Xavier Altafaj; Weijun Cheng; Eric Estève; Julie Urbani; Didier Grunwald; Jean-Marc Sabatier; Roberto Coronado; Michel De Waard; Michel Ronjat
Journal:  J Biol Chem       Date:  2004-12-09       Impact factor: 5.157

6.  Multiple loops of the dihydropyridine receptor pore subunit are required for full-scale excitation-contraction coupling in skeletal muscle.

Authors:  Leah Carbonneau; Dipankar Bhattacharya; David C Sheridan; Roberto Coronado
Journal:  Biophys J       Date:  2005-04-22       Impact factor: 4.033

7.  Charged surface area of maurocalcine determines its interaction with the skeletal ryanodine receptor.

Authors:  Balázs Lukács; Mónika Sztretye; János Almássy; Sándor Sárközi; Beatrix Dienes; Kamel Mabrouk; Cecilia Simut; László Szabó; Péter Szentesi; Michel De Waard; Michel Ronjat; István Jóna; László Csernoch
Journal:  Biophys J       Date:  2008-07-11       Impact factor: 4.033

8.  Recombinant expression of Intrepicalcin from the scorpion Vaejovis intrepidus and its effect on skeletal ryanodine receptors.

Authors:  Leonel Vargas-Jaimes; Liang Xiao; Jing Zhang; Lourival D Possani; Héctor H Valdivia; Verónica Quintero-Hernández
Journal:  Biochim Biophys Acta Gen Subj       Date:  2017-01-31       Impact factor: 3.770

9.  Lanthanides Report Calcium Sensor in the Vestibule of Ryanodine Receptor.

Authors:  Sándor Sárközi; István Komáromi; István Jóna; János Almássy
Journal:  Biophys J       Date:  2017-05-23       Impact factor: 4.033

10.  Multiple actions of phi-LITX-Lw1a on ryanodine receptors reveal a functional link between scorpion DDH and ICK toxins.

Authors:  Jennifer J Smith; Irina Vetter; Richard J Lewis; Steve Peigneur; Jan Tytgat; Alexander Lam; Esther M Gallant; Nicole A Beard; Paul F Alewood; Angela F Dulhunty
Journal:  Proc Natl Acad Sci U S A       Date:  2013-05-13       Impact factor: 11.205

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