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Difference between revisions of "Perry 2011 Biochem J"

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{{Labeling
{{Labeling
|area=Respiration
|organism=Human, Rat
|organism=Human, Rat
|tissues=Skeletal muscle
|tissues=Skeletal muscle
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|enzymes=Complex I, Complex V; ATP Synthase
|enzymes=Complex I, Complex V; ATP Synthase
|injuries=Temperature
|injuries=Temperature
|topics=ATP; ADP; AMP; PCr
|topics=ADP, Inhibitor
|substratestates=CI
|substratestates=CI
|kinetics=Inhibitor; Uncoupler
|instruments=Oxygraph-2k
|instruments=Oxygraph-2k
}}
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Revision as of 13:42, 11 August 2013

Publications in the MiPMap
Perry CG, Kane DA, Lin CT, Kozy R, Cathey BL, Lark DS, Kane CL, Brophy PM, Gavin TP, Anderson EJ, Neufer PD (2011) Inhibiting myosin-ATPase reveals a dynamic range of mitochondrial respiratory control in skeletal muscle. Biochem J 437: 215-222.

» PMID:21554250

Perry CG, Kane DA, Lin CT, Kozy R, Cathey BL, Lark DS, Kane CL, Brophy PM, Gavin TP, Anderson EJ, Neufer PD (2011) Biochem J

Abstract: Assessment of mitochondrial ADP-stimulated respiratory kinetics in PmFBs (permeabilized fibre bundles) is increasingly used in clinical diagnostic and basic research settings. However, estimates of the Km for ADP vary considerably (~20-300 μM) and tend to overestimate respiration at rest. Noting that PmFBs spontaneously contract during respiration experiments, we systematically determined the impact of contraction, temperature and oxygenation on ADP-stimulated respiratory kinetics. BLEB (blebbistatin), a myosin II ATPase inhibitor, blocked contraction under all conditions and yielded high Km values for ADP of >~250 and ~80 μM in red and white rat PmFBs respectively. In the absence of BLEB, PmFBs contracted and the Km for ADP decreased ~2-10-fold in a temperature-dependent manner. PmFBs were sensitive to hyperoxia (increased Km) in the absence of BLEB (contracted) at 30 °C but not 37 °C. In PmFBs from humans, contraction elicited high sensitivity to ADP (Km<100 μM), whereas blocking contraction (+BLEB) and including a phosphocreatine/creatine ratio of 2:1 to mimic the resting energetic state yielded a Km for ADP of ~1560 μM, consistent with estimates of in vivo resting respiratory rates of <1% maximum. These results demonstrate that the sensitivity of muscle to ADP varies over a wide range in relation to contractile state and cellular energy charge, providing evidence that enzymatic coupling of energy transfer within skeletal muscle becomes more efficient in the working state. Keywords: Bioenergetics, Blebbistatin, Creatine kinase, Myosin-ATPase, N-benzyltoluene sulfonamide, Skeletal muscle contraction

O2k-Network Lab: US_NC Greenville_Neufer PD, CA Toronto Perry CG, US_NC_Greenville_Anderson EJ, CA_Antigonish_Kane DA, US NC Greenville East Carolina Univ


Labels: MiParea: Respiration 

Stress:Temperature  Organism: Human, Rat  Tissue;cell: Skeletal muscle  Preparation: Permeabilized tissue  Enzyme: Complex I, Complex V; ATP Synthase"Complex V; ATP Synthase" is not in the list (Adenine nucleotide translocase, Complex I, Complex II;succinate dehydrogenase, Complex III, Complex IV;cytochrome c oxidase, Complex V;ATP synthase, Inner mt-membrane transporter, Marker enzyme, Supercomplex, TCA cycle and matrix dehydrogenases, ...) of allowed values for the "Enzyme" property.  Regulation: ADP, Inhibitor 


HRR: Oxygraph-2k