Biomedical Engineering Reference
In-Depth Information
Fig. 4.3
Left : fitting results with the model by Hai and Murphy ( 1988 ) where the active stress is
n AMp
+
n AM and the myosin phosphorylation is n Mp
+
n AMp . The phosphorylating reaction rates
k 1 and k 6 were set to 0 . 35 s 1
for 5 s followed by 0 . 085 s 1 . The other reaction rates were set to
0 . 1s 1 , k 4
0 . 11 s 1 , k 3
0 . 44 s 1
0 . 005 s 1 . Right : steady-state values
k 2
=
k 5
=
=
=
and k 7
=
of the sum of fractions n AMp
+
n AM and n Mp
+
n AMp for different values of the phosphorylating
reaction rates k 1 and k 6 (Hai and Murphy, 1988 )
can be summarized by the following system of differential equations, i.e.
=
n M
n Mp
n AMp
n AM
k 1
k 2
0
k 7
n M
n Mp
n AMp
n AM
d
d t
k 1
(k 2 +
k 3 )
k 4
0
,
0
k 3
(k 4 +
k 5 )
k 6
0
0
k 5
(k 6 +
k 7 )
(4.1)
where n M , n Mp , n AMp and n AM are fractions of the myosin functional states M, Mp,
AMp, AM, with the constraint n M +
0 and k 1 ,...,k 7
are reaction rates describing the transition between the different functional states.
Hence, the reaction rates k 1 and k 6 represents the phosphorylation of M to Mp and
AM to AMp by the MLCK activity and the reaction rates k 2 and k 5 represents
the dephosphorylation of Mp to M and AMp to AM by the MLCP activity. The
reaction rates k 3 and k 4 represents the attachment and detachment of the cycling
phosphorylated cross-bridges and the reaction rates k 7 represents the detachment
of the latch-bridges. The phosphorylating reaction rates k 1 and k 6 can be coupled
to the internal and also the external
n Mp +
n AMp +
n AM =
1, n i
Ca 2 + ]
. Figure 4.3 shows the evolution of the
different fraction of the functional states with time using the model by Hai and
Murphy ( 1988 ).
When assuming maximal stimulated activation the phosphorylating MLCK ac-
tivity can be related and coupled to the extracellular
[
Ca 2 + ]
. In Murtada et al.
( 2010a ) a Michaelis-Menten kinetics characteristic of the MLCK activity was im-
plemented. The rate constants k 1 and k 6 are expressed as
[
2
α Ca 2 + e ,
[
CaCaM
]
k 1 =
k 6 =
,
[
CaCaM
]=
(4.2)
K CaCaM
2
[
CaCaM
]
+
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