Literature DB >> 8594553

The influence of ionic strength upon relaxation from rigor induced by flash photolysis of caged-ATP in skinned murine skeletal muscle fibres.

C Veigel1, R D v Maydell, R Wiegand-Steubing, R Goody, H A Fink.   

Abstract

The influence of ionic strength upon relaxation kinetics from rigor in skinned murine extensor digitorum longus (EDL) skeletal muscle fibres was examined using photolysis of caged-ATP at low Ca2+. The ionic strength was adjusted with either KMeSO3 or ethylene glycolbis-(beta-aminoethyl ether) N,N,N',N'-tetraacetic acid, dipotassium salt (K2EGTA) in the range of tau /2 = 65-215mM, or I.E. 49-194mM, where I.E. denotes ionic equivalent. Following rigor development at a tau /2 of 165-215mM (I.E. 144-194mM), the liberation of approximately 0.5mM ATP resulted in an initial 6-to 10-ms detachment phase with a decline in force of approximately 10-20% followed by a 10-to 30-ms reattachment with up to a 60% increase compared to the corresponding rigor level and a final detachment leading to complete relaxation. Interestingly, when similar ATP concentrations were liberated at lower ionic strengths between a tau /2 of 65mM and 110mM (I.E. 60-100mM), the initial detachment phase was shortened and force decreased by only approximately 5-10%, while the following reattachment phase was lengthened and led to an increased steady-state force of approximately 20-80% without final relaxation. ATP-induced detachment and subsequent reattachment were mainly determined by the currently present ionic strength and were relatively independent of the preceding rigor state which had been developed at higher or lower ionic strengths. The effects of phosphate and apyrase on the force transient suggest that reattachment of ADP- binding crossbridges may contribute to the increase in tension at high and even more at low ionic strengths. The study shows that the kinetics of initial fast relaxation and subsequent redevelopment of force following flash photolysis of similar ATP concentrations are markedly modified by the ionic strength in the narrow range of between 65mM and 215mM.

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Year:  1995        PMID: 8594553     DOI: 10.1007/bf01837414

Source DB:  PubMed          Journal:  Pflugers Arch        ISSN: 0031-6768            Impact factor:   3.657


  28 in total

1.  Effect of ionic strength on crossbridge kinetics as studied by sinusoidal analysis, ATP hydrolysis rate and X-ray diffraction techniques in chemically skinned rabbit psoas fibres.

Authors:  M Kawai; J S Wray; K Güth
Journal:  J Muscle Res Cell Motil       Date:  1990-10       Impact factor: 2.698

Review 2.  The dynamics of actin and myosin association and the crossbridge model of muscle contraction.

Authors:  M A Geeves
Journal:  Biochem J       Date:  1991-02-15       Impact factor: 3.857

3.  Relaxation from rigor by photolysis of caged-ATP in different types of muscle fibres from Xenopus laevis.

Authors:  G J Stienen; M A Ferenczi
Journal:  J Muscle Res Cell Motil       Date:  1991-12       Impact factor: 2.698

4.  Potentiometric measurements of stoichiometric and apparent affinity constants of EGTA for protons and divalent ions including calcium.

Authors:  G L Smith; D J Miller
Journal:  Biochim Biophys Acta       Date:  1985-05-08

5.  Calculator programs for computing the composition of the solutions containing multiple metals and ligands used for experiments in skinned muscle cells.

Authors:  A Fabiato; F Fabiato
Journal:  J Physiol (Paris)       Date:  1979

6.  Initiation of active contraction by photogeneration of adenosine-5'-triphosphate in rabbit psoas muscle fibres.

Authors:  Y E Goldman; M G Hibberd; D R Trentham
Journal:  J Physiol       Date:  1984-09       Impact factor: 5.182

7.  Effects of ionic strength on force transients induced by flash photolysis of caged ATP in covalently crosslinked rabbit psoas muscle fibers.

Authors:  K Yamada; Y Emoto; K Horiuti; K Tawada
Journal:  Adv Exp Med Biol       Date:  1993       Impact factor: 2.622

8.  Kinetics of relaxation from rigor of permeabilized fast-twitch skeletal fibers from the rabbit using a novel caged ATP and apyrase.

Authors:  H Thirlwell; J E Corrie; G P Reid; D R Trentham; M A Ferenczi
Journal:  Biophys J       Date:  1994-12       Impact factor: 4.033

9.  Three-dimensional structure of myosin subfragment-1: a molecular motor.

Authors:  I Rayment; W R Rypniewski; K Schmidt-Bäse; R Smith; D R Tomchick; M M Benning; D A Winkelmann; G Wesenberg; H M Holden
Journal:  Science       Date:  1993-07-02       Impact factor: 47.728

10.  Ion-specific and general ionic effects on contraction of skinned fast-twitch skeletal muscle from the rabbit.

Authors:  M A Andrews; D W Maughan; T M Nosek; R E Godt
Journal:  J Gen Physiol       Date:  1991-12       Impact factor: 4.086

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