Perry 2011 Biochem J: Difference between revisions

From Bioblast
No edit summary
No edit summary
Line 1: Line 1:
{{Publication
{{Publication
|title=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.
|title=Perry CGR, 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.
|info=[http://www.ncbi.nlm.nih.gov/pubmed/21554250 PMID:21554250]
|info=[http://www.ncbi.nlm.nih.gov/pubmed/21554250 PMID:21554250]
|authors=Perry CG, Kane DA, Lin CT, Kozy R, Cathey BL, Lark DS, Kane CL, Brophy PM, Gavin TP, Anderson EJ, Neufer PD
|authors=Perry CGR, Kane DA, Lin CT, Kozy R, Cathey BL, Lark DS, Kane CL, Brophy PM, Gavin TP, Anderson EJ, Neufer PD
|year=2011
|year=2011
|journal=Biochem J
|journal=Biochem J

Revision as of 11:59, 10 September 2012

Publications in the MiPMap
Perry CGR, 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.

ยป PMID:21554250

Perry CGR, 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 ฮผM) 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 ฮผM 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 ยฐC but not 37 ยฐC. In PmFBs from humans, contraction elicited high sensitivity to ADP (Km<100 ฮผM), 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 ฮผM, 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. โ€ข Keywords: bioenergetics, blebbistatin, creatine kinase, myosin-ATPase, N-benzyltoluene sulfonamide, skeletal muscle contraction

โ€ข O2k-Network Lab: US_NC Greenville_Neufer PD, US_NC_Greenville_Anderson EJ, CA_Antigonish_Kane DA


Labels:


Organism: Human, Rat  Tissue;cell: Skeletal muscle  Preparation: Permeabilized tissue 



HRR: Oxygraph-2k 


Cookies help us deliver our services. By using our services, you agree to our use of cookies.