First published online April 20, 2007
Journal of Experimental Biology 210, 1576-1583 (2007)
Published by The Company of Biologists 2007
doi: 10.1242/jeb.000133
Computational biology of cardiac myocytes: proposed standards for the physiome
Nicolas P. Smith1,2,*,
Edmund J. Crampin2,
Steven A. Niederer1,2,
James B. Bassingthwaighte3 and
Daniel A. Beard4
1 University Computing Laboratory, University of Oxford, Oxford, OX1 3QD,
UK
2 Bioengineering Institute, University of Auckland, Auckland, New
Zealand
3 University of Washington, Seattle, USA
4 Medical College Wisconsin, WI, USA

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Fig. 1. Schematic diagrams of (A) a `thermodynamic box' representation of an
enzymatic cycle coupled to ATP hydrolysis, as used to model the sodium pump,
and (B) the electrophysiological, contraction and pH regulatory components in
the coupled myocyte model. E, enzyme; I, current. Other abbreviations
and further explanation are available elsewhere
(Crampin and Smith, 2006 ).
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Fig. 2. (A) Isometric tension data at varying strains. Solid data points represent
measurements taken under physiological conditions used to fit the model. The
remaining data are plotted as crosses. (B) Schematic diagram of the model of
muscle cell oxidative energy metabolism.
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Fig. 4. Citation tree for the source of the (A) binding affinity of Ca2+
to troponin C and (B) binding affinity of Ca2+ to calsequestrin
parameter, in cardiac myocyte mathematical models. Grey and white boxes
indicate experimental and modelling studies, respectively.
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© The Company of Biologists Ltd 2007