3D structure of muscle dihydropyridine receptor

Excitation contraction coupling, the rapid and massive Ca2+ release under control of an action potential that triggers muscle contraction, takes places at specialized regions of the cell called triad junctions. There, a highly ordered supramolecular complex between the dihydropyridine receptor (DHPR...

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Main Author: Montserrat Samsó (Author)
Format: Book
Published: PAGEPress Publications, 2015-01-01T00:00:00Z.
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100 1 0 |a Montserrat Samsó  |e author 
245 0 0 |a 3D structure of muscle dihydropyridine receptor 
260 |b PAGEPress Publications,   |c 2015-01-01T00:00:00Z. 
500 |a 2037-7452 
500 |a 2037-7460 
500 |a 10.4081/ejtm.2015.4840 
520 |a Excitation contraction coupling, the rapid and massive Ca2+ release under control of an action potential that triggers muscle contraction, takes places at specialized regions of the cell called triad junctions. There, a highly ordered supramolecular complex between the dihydropyridine receptor (DHPR) and the ryanodine receptor (RyR1) mediates the quasi‐instantaneous conversion from T‐tubule depolarization into Ca2+ release from the sarcoplasmic reticulum (SR). The DHPR has several key modules required for EC coupling: the voltage sensors and II‐III loop in the alpha1s subunit, and the beta subunit. To gain insight into their molecular organization, this review examines the most updated 3D structure of the DHPR as obtained by transmission electron microscopy and image reconstruction. Although structure determination of a heteromeric membrane protein such as the DHPR is challenging, novel technical advances in protein expression and 3D labeling facilitated this task. The 3D structure of the DHPR complex consists of a main body with five irregular corners around its perimeter encompassing the transmembrane alpha 1s subunit besides the intracellular beta subunit, an extended extracellular alpha 2 subunit, and a bulky intracellular II‐III loop. The structural definition attained at 19 Å resolution enabled docking of the atomic coordinates of structural homologs of the alpha1s and beta subunits. These structural features, together with their relative location with respect to the RyR1, are discussed in the context of the functional data. 
546 |a EN 
690 |a dihydropyridine receptor, excitation‐contraction coupling, transmission electron microscopy, 3D reconstruction 
690 |a Medicine 
690 |a R 
690 |a Human anatomy 
690 |a QM1-695 
655 7 |a article  |2 local 
786 0 |n European Journal of Translational Myology, Vol 25, Iss 1, Pp 27-33 (2015) 
787 0 |n http://pagepressjournals.org/index.php/bam/article/view/4840 
787 0 |n https://doaj.org/toc/2037-7452 
787 0 |n https://doaj.org/toc/2037-7460 
856 4 1 |u https://doaj.org/article/01ab9ab6a64c46159b5dfc3dbe78724e  |z Connect to this object online.