Literature DB >> 7560004

Alternate disposition of tetrads in peripheral couplings of skeletal muscle.

C Franzini-Armstrong1, J W Kish.   

Abstract

The sarcoplasmic reticulum forms junctions with the surface membrane (peripheral couplings), which are structurally and functionally equivalent to the junctions between sarcoplasmic reticulum and transverse tubules (triads and dyads). Feet (ryanodine receptors, or sarcoplasmic reticulum calcium release channels) are disposed in arrays in the junctional sarcoplasmic reticulum membrane. Tetrads (groups of four dihydropyridine receptors, each called a unit) are disposed in ordered arrays in junctional domains of transverse tubules and surface membrane. We measured three parameters of tetrad arrays in peripheral couplings from three different species: (1) the centre-to-centre distances between tetrads (intertetrad spacing); (2) the angle between lines joining tetrad units and those joining the centres of tetrads (skew angle); (3) the centre-to-centre distance between tetrad units (intratetrad spacing). These measurements are compared with those predicted from models of feet and tetrad arrays. Intratetrad spacings and skew angles are consistent with an interaction of tetrads with alternate feet and with a location of tetrad units over feet subunits. The slightly larger size of the intratetrad spacing relative to the distance between feet subunits indicates that tetrads may be larger than feet, despite the fact that the molecular weight of DHPRs is less than that of feet subunits. This is offered as a possible explanation for the association of tetrads with alternate feet. Arrays of tetrads tend to be incomplete in images from freeze-fractures, due to lack of some of the units composing the tetrads.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1995        PMID: 7560004     DOI: 10.1007/bf00121140

Source DB:  PubMed          Journal:  J Muscle Res Cell Motil        ISSN: 0142-4319            Impact factor:   2.698


  12 in total

Review 1.  The mechanical hypothesis of excitation-contraction (EC) coupling in skeletal muscle.

Authors:  E Ríos; J J Ma; A González
Journal:  J Muscle Res Cell Motil       Date:  1991-04       Impact factor: 2.698

2.  Restoration of junctional tetrads in dysgenic myotubes by dihydropyridine receptor cDNA.

Authors:  H Takekura; L Bennett; T Tanabe; K G Beam; C Franzini-Armstrong
Journal:  Biophys J       Date:  1994-08       Impact factor: 4.033

3.  Freeze-fracture of frog slow tonic fibers. Structure of surface and internal membranes.

Authors:  C Franzini-Armstrong
Journal:  Tissue Cell       Date:  1984       Impact factor: 2.466

4.  Freeze-fracture electronmicroscopic analysis of plasma membranes of cultured muscle cells in Duchenne dystrophy.

Authors:  M Osame; A G Engel; C J Rebouche; R E Scott
Journal:  Neurology       Date:  1981-08       Impact factor: 9.910

5.  Ratio of ryanodine to dihydropyridine receptors in cardiac and skeletal muscle and implications for E-C coupling.

Authors:  D M Bers; V M Stiffel
Journal:  Am J Physiol       Date:  1993-06

6.  Muscle fibers from dysgenic mouse in vivo lack a surface component of peripheral couplings.

Authors:  C Franzini-Armstrong; M Pincon-Raymond; F Rieger
Journal:  Dev Biol       Date:  1991-08       Impact factor: 3.582

7.  High-affinity [3H]PN200-110 and [3H]ryanodine binding to rabbit and frog skeletal muscle.

Authors:  K Anderson; A H Cohn; G Meissner
Journal:  Am J Physiol       Date:  1994-02

8.  Molecular architecture of membranes involved in excitation-contraction coupling of cardiac muscle.

Authors:  X H Sun; F Protasi; M Takahashi; H Takeshima; D G Ferguson; C Franzini-Armstrong
Journal:  J Cell Biol       Date:  1995-05       Impact factor: 10.539

9.  Subunit structure of junctional feet in triads of skeletal muscle: a freeze-drying, rotary-shadowing study.

Authors:  D G Ferguson; H W Schwartz; C Franzini-Armstrong
Journal:  J Cell Biol       Date:  1984-11       Impact factor: 10.539

10.  Structural evidence for direct interaction between the molecular components of the transverse tubule/sarcoplasmic reticulum junction in skeletal muscle.

Authors:  B A Block; T Imagawa; K P Campbell; C Franzini-Armstrong
Journal:  J Cell Biol       Date:  1988-12       Impact factor: 10.539

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  29 in total

Review 1.  Calcium release in skeletal muscle: from K+ contractures to Ca2+ sparks.

Authors:  C Caputo
Journal:  J Muscle Res Cell Motil       Date:  2001       Impact factor: 2.698

2.  The structure of Ca(2+) release units in arthropod body muscle indicates an indirect mechanism for excitation-contraction coupling.

Authors:  Hiroaki Takekura; Clara Franzini-Armstrong
Journal:  Biophys J       Date:  2002-11       Impact factor: 4.033

3.  Structure of the voltage-gated L-type Ca2+ channel by electron cryomicroscopy.

Authors:  I I Serysheva; S J Ludtke; M R Baker; W Chiu; S L Hamilton
Journal:  Proc Natl Acad Sci U S A       Date:  2002-07-29       Impact factor: 11.205

4.  Orthograde dihydropyridine receptor signal regulates ryanodine receptor passive leak.

Authors:  José Miguel Eltit; Hongli Li; Christopher W Ward; Tadeusz Molinski; Isaac N Pessah; Paul D Allen; José R Lopez
Journal:  Proc Natl Acad Sci U S A       Date:  2011-04-11       Impact factor: 11.205

5.  Modulation of the oligomerization of isolated ryanodine receptors by their functional states.

Authors:  Xiao-Fang Hu; Xin Liang; Ke-Ying Chen; Hong Xie; Yuhong Xu; Pei-Hong Zhu; Jun Hu
Journal:  Biophys J       Date:  2005-06-10       Impact factor: 4.033

6.  De novo reconstitution reveals the proteins required for skeletal muscle voltage-induced Ca2+ release.

Authors:  Stefano Perni; Manuela Lavorato; Kurt G Beam
Journal:  Proc Natl Acad Sci U S A       Date:  2017-12-11       Impact factor: 11.205

7.  Differential contribution of skeletal and cardiac II-III loop sequences to the assembly of dihydropyridine-receptor arrays in skeletal muscle.

Authors:  Hiroaki Takekura; Cecilia Paolini; Clara Franzini-Armstrong; Gerlinde Kugler; Manfred Grabner; Bernhard E Flucher
Journal:  Mol Biol Cell       Date:  2004-09-22       Impact factor: 4.138

8.  Effect of sarcoplasmic reticulum (SR) calcium content on SR calcium release elicited by small voltage-clamp depolarizations in frog cut skeletal muscle fibers equilibrated with 20 mM EGTA.

Authors:  P C Pape; N Carrier
Journal:  J Gen Physiol       Date:  1998-08       Impact factor: 4.086

9.  An Ryr1I4895T mutation abolishes Ca2+ release channel function and delays development in homozygous offspring of a mutant mouse line.

Authors:  Elena Zvaritch; Frederic Depreux; Natasha Kraeva; Ryan E Loy; Sanjeewa A Goonasekera; Simona Boncompagni; Simona Boncompagi; Alexander Kraev; Anthony O Gramolini; Robert T Dirksen; Clara Franzini-Armstrong; Christine E Seidman; J G Seidman; David H Maclennan
Journal:  Proc Natl Acad Sci U S A       Date:  2007-11-14       Impact factor: 11.205

10.  Organization of Ca2+ release units in excitable smooth muscle of the guinea-pig urinary bladder.

Authors:  Edwin D Moore; Tilman Voigt; Yvonne M Kobayashi; Gerrit Isenberg; Fred S Fay; Maria F Gallitelli; Clara Franzini-Armstrong
Journal:  Biophys J       Date:  2004-09       Impact factor: 4.033

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