Chapter 14 Functional and Structural Approaches to the Study of Excitation--Contraction Coupling
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An explant muscle model to examine the refinement of the synaptic landscape
2014, Journal of Neuroscience MethodsCitation Excerpt :The voltage of the action potential travels through the t-tubule conduits to depolarize the dihydropyridine receptor (DHPR, CaV1.1), which mechanically opens ryanodine receptor type 1 (RyR1) channels in the sarcoplasmic reticulum (SR). RyR1 channels release intracellular calcium stores to flood the myofiber with calcium, which initiates muscle contraction, known as excitation–contraction (E–C) coupling, to permit locomotion (Beam and Franzini-Armstrong, 1997; Takeshima et al., 1994). As shown above, nerve-dependent signals are required for AChR cluster redistribution.
Fluorescence Resonance Energy Transfer (FRET) indicates that association with the type I ryanodine receptor (RyR1) causes reorientation of multiple cytoplasmic domains of the dihydropyridine receptor (DHPR) α<inf>1s</inf> subunit
2012, Journal of Biological ChemistryCitation Excerpt :YPet was attached to the N terminus of the first α1S via a 12-residue linker (SRAQASNSAVD) and CyPet was attached to the C terminus of the second α1S via a four-residue linker (PVAT). Myoblasts were prepared from newborn dysgenic mice, homozygous for absence of α1S (28), or newborn dyspedic mice, homozygous for absence of RyR1 (29) as described (30). The myoblasts were grown for 6–7 days in a humidified 37 °C incubator with 5% CO2 in Dulbecco's modified eagle medium (E15-009, PAA, Coelbe, Germany), supplemented with 10% fetal bovine serum/10% horse serum (Biochrom, Berlin, Germany).
Excitation-transcription coupling in sympathetic neurons and the molecular mechanism of its initiation
2011, Neuroscience Research