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Difference between revisions of "Garlid KD 2012 Abstract Bioblast"

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{{Abstract
{{Abstract
|title=Garlid KD (2012) Bioenergetics: A Physiological Overview. Mitochondr Physiol Network 17.12.
|title=Garlid KD (2012) Bioenergetics: a physiological overview. Mitochondr Physiol Network 17.12.
|info=[[MiPNet17.12 Bioblast 2012|MiPNet17.12 Bioblast 2012 - Open Access]]
|info=[[MiPNet17.12 Bioblast 2012|MiPNet17.12 Bioblast 2012 - Open Access]]
|authors=Garlid KD
|authors=Garlid KD
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|event=[[Bioblast 2012]]
|event=[[Bioblast 2012]]
|abstract=[[File:Keith Pic.jpg|right|200px|Garlid Keith]]
|abstract=[[File:Keith Pic.jpg|right|200px|Garlid Keith]]
The chemiosmotic theory, for which Peter Mitchell was awarded the Nobel Prize in Chemistry, was presented as a hypothesis far in advance of experimental evidence, and it stands as a glorious monument to the scientific method. Mitchell [1] proposed that nature uses protonic batteries to drive ATP synthesis and that biological energy conservation is essentially a problem in membrane transport. This was summarized in four postulates: 1) The electron transport system is vectorially oriented so that the energy of electron transport drives ejection of protons from the matrix, creating a proton electrochemical potential gradient. 2) The F<sub>1</sub>F<sub>O</sub> ATPase is also vectorially oriented so that the energy of ATP hydrolysis drives ejection of protons from the matrix. Because it is reversible, protons driven inward through the enzyme by the protonmotive force will cause ATP synthesis. 3) Ion leaks would short-circuit the protonmotive batteries, so the inner membrane must have a low diffusive permeability to ions in general and to protons in particular. 4) Cation leaks are compensated by electroneutral cation/proton antiporters, and low permeability for substrate anions is compensated by electroneutral anion exchange porters. Each of these postulates was, at the time, a radical departure from conventional wisdom. Postulates 3 and 4 form the basis for one aspect of mitochondrial physiology, but mitochondrial physiology is a rich and varied field, and includes cellular processes such as autophagy, fission/fusion, and apoptosis. In a brief talk, it will be necessary to focus on one aspect, and I will review recent progress in understanding the K<sup>+</sup> cycle and its role in the cell.Β  Β 
The chemiosmotic theory, for which Peter Mitchell was awarded the Nobel Prize in Chemistry, was presented as a hypothesis far in advance of experimental evidence, and it stands as a glorious monument to the scientific method. Mitchell [1] proposed that nature uses protonic batteries to drive ATP synthesis and that biological energy conservation is essentially a problem in membrane transport. This was summarized in four postulates: (1) The electron transport system is vectorially oriented so that the energy of electron transport drives ejection of protons from the matrix, creating a proton electrochemical potential gradient. (2) The F<sub>1</sub>F<sub>O</sub> ATPase is also vectorially oriented so that the energy of ATP hydrolysis drives ejection of protons from the matrix. Because it is reversible, protons driven inward through the enzyme by the protonmotive force will cause ATP synthesis. (3) Ion leaks would short-circuit the protonmotive batteries, so the inner membrane must have a low diffusive permeability to ions in general and to protons in particular. (4) Cation leaks are compensated by electroneutral cation/proton antiporters, and low permeability for substrate anions is compensated by electroneutral anion exchange porters. Each of these postulates was, at the time, a radical departure from conventional wisdom. Postulates 3 and 4 form the basis for one aspect of mitochondrial physiology, but mitochondrial physiology is a rich and varied field, and includes cellular processes such as autophagy, fission/fusion, and apoptosis. In a brief talk, it will be necessary to focus on one aspect, and I will review recent progress in understanding the K<sup>+</sup> cycle and its role in the cell.Β  Β 
Β 
# [http://onlinelibrary.wiley.com/doi/10.1111/j.1469-185X.1966.tb01501.x/abstract Mitchell P (2008) Chemiosmotic coupling in oxidative and photosynthetic phosphorylation. Biol Rev 41: 445-501.]
# [http://onlinelibrary.wiley.com/doi/10.1111/j.1469-185X.1966.tb01501.x/abstract Mitchell P (2008) Chemiosmotic coupling in oxidative and photosynthetic phosphorylation. Biological Reviews 41: 445-501.]
|keywords=Chemiosmosis, ATP synthesis and hydrolysis, K+ cycling
|keywords=Chemiosmosis, ATP synthesis and hydrolysis, K+ cycling
|journal=Mitochondr Physiol Network
|journal=Mitochondr Physiol Network
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}}
}}
{{Labeling
{{Labeling
|enzymes=Complex V;ATP synthase
|topics=ATP, Ion;substrate transport
|instruments=Theory
|instruments=Theory
|enzymes=Complex V; ATP Synthase
|additional=Langendorff Perfused Heart
|topics=Ion Homeostasis, ATP; ADP; AMP; PCr
|journal=Mitochondr Physiol Network
|journal=Mitochondr Physiol Network
|articletype=Abstract
|articletype=Abstract
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== Help ==
== Help ==
* [[Abstracts help]]
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Latest revision as of 16:24, 25 November 2015

Garlid KD (2012) Bioenergetics: a physiological overview. Mitochondr Physiol Network 17.12.

Link: MiPNet17.12 Bioblast 2012 - Open Access

Garlid KD (2012)

Event: Bioblast 2012

Garlid Keith

The chemiosmotic theory, for which Peter Mitchell was awarded the Nobel Prize in Chemistry, was presented as a hypothesis far in advance of experimental evidence, and it stands as a glorious monument to the scientific method. Mitchell [1] proposed that nature uses protonic batteries to drive ATP synthesis and that biological energy conservation is essentially a problem in membrane transport. This was summarized in four postulates: (1) The electron transport system is vectorially oriented so that the energy of electron transport drives ejection of protons from the matrix, creating a proton electrochemical potential gradient. (2) The F1FO ATPase is also vectorially oriented so that the energy of ATP hydrolysis drives ejection of protons from the matrix. Because it is reversible, protons driven inward through the enzyme by the protonmotive force will cause ATP synthesis. (3) Ion leaks would short-circuit the protonmotive batteries, so the inner membrane must have a low diffusive permeability to ions in general and to protons in particular. (4) Cation leaks are compensated by electroneutral cation/proton antiporters, and low permeability for substrate anions is compensated by electroneutral anion exchange porters. Each of these postulates was, at the time, a radical departure from conventional wisdom. Postulates 3 and 4 form the basis for one aspect of mitochondrial physiology, but mitochondrial physiology is a rich and varied field, and includes cellular processes such as autophagy, fission/fusion, and apoptosis. In a brief talk, it will be necessary to focus on one aspect, and I will review recent progress in understanding the K+ cycle and its role in the cell.

  1. Mitchell P (2008) Chemiosmotic coupling in oxidative and photosynthetic phosphorylation. Biol Rev 41: 445-501.

β€’ Keywords: Chemiosmosis, ATP synthesis and hydrolysis, K+ cycling


Labels:



Enzyme: Complex V;ATP synthase  Regulation: ATP, Ion;substrate transport 


HRR: Theory 

Langendorff Perfused Heart 



Affiliations and author contributions

Keith D Garlid: Dept of Biology, Portland State University, Portland, OR, USA; Email: [email protected]

Figure 1

Schemata of ATP_Synthase_proton gradient

Coupling of electron transport with ATP synthesis. Protons are ejected electrogenically by the electron transport chain, generating a protonmotive force. This drives protons back through the ATPsynthase, leading to ATP production. Some of the energy is dissipated by electrophoretic back-diffusion, primarily of K+ and H+. Also necessary for ATP synthesis are the adenine nucleotide translocase, which catalyzes electrophoretic ATP/ADP exchange, and the phosphate transporter, which catalyzes electroneutral phosphate uptake. A considerable amount of mitochondrial physiology, including volume homeostasis, Ca2+ regulation, regulation of ROS production, and intramitochondrial signaling, is governed by inner membrane cation porters for Na+, K+ and Ca2+.

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