Aarhus University Seal / Aarhus Universitets segl

Sergey Fedosov

Creatine-creatine phosphate shuttle modeled as two-compartment system at different levels of creatine kinase activity

Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisTidsskriftartikelForskningpeer review

Dokumenter

In order to characterize ADP-ATP and creatine-creatine phosphate (Cr-CrP) shuttles a minimal mathematical model with two compartments and cyclic turnover of matter was designed. The 'mitochondrial' compartment contained 'ATP-synthase' and 'mitochondrial ereatine kinase' (mitCK). The 'cytoplasmic' compartment consisted of 'ATPase', 'cytoplasmic creatine kinase' (cytCK) and an
'ADP-binding structure'. The exchange of metabolites between these compartments was limited. Different levels of cytCK and mitCK
expression as welt as different exchange rate constants between the compartments were assigned to obtain several different modes. Every
steady state obtained in the presence of low ATPase activity ('resting' conditions) was then disturbed by a steep activation of ATPase
('muscle performance') and afterwards the transition to a new steady state was followed in time. The ATP-buffering capacity of the system initially acquired by cytCK expression significantly increased after additional mitCK supplement. Nevertheless, even the complete Cr-CrP shuttle failed to maintain a high [ATP]/[ADP] ratio during long term 'muscle performance' due to the rate limiting
CK-transphosphorylation in the mitochondria. The facilitated diffusion of Cr and CrP was not critical, and the model worked with the same efficiency even at equal permeabilities for nucleotides and guanidines. Under 'resting conditions' the main flux of matter went through the Cr-CrP shuttle, resulting in 'pumping' of CrP. This ensured a 40 s delay in the [ATP] decrease at 'work'. The partial systems without mitCK were not as effective, and this delay was 0-10 s. However, the ADP-ATP shuttle was of more importance at the steady
state achieved under ' working' conditions
OriginalsprogEngelsk
TidsskriftBiochimica et Biophysica Acta - Protein Structure and Molecular Enzymology
Vol/bind1208
Nummer2
Sider (fra-til)238-246
Antal sider9
ISSN0167-4838
StatusUdgivet - 1994

Se relationer på Aarhus Universitet Citationsformater

Download-statistik

Ingen data tilgængelig

ID: 45299578