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In essence, the Goldman formula expresses the membrane potential as a weighted average of the reversal potentials for the individual ion types, weighted by permeability. (Although the membrane potential changes about 100 mV during an action potential, the concentrations of ions inside and outside the cell do not change significantly.
It is an active pump that generates a proton concentration gradient across the inner mitochondrial membrane, because there are more protons outside the matrix than inside. The difference in pH and electric charge (ignoring differences in buffer capacity) creates an electrochemical potential difference that works similar to that of a battery or ...
The final step of cellular respiration is the electron transport chain, composed of four complexes embedded in the inner mitochondrial membrane. Complexes I, III, and IV pump protons from the matrix to the intermembrane space (IMS); for every electron pair entering the chain, ten protons translocate into the IMS.
Mitochondria present in all cells in the human body require a resting membrane potential of the inner mitochondrial membrane to synthesize adenosine triphosphate (ATP). This membrane polarity is established through a series of proton pumps transporting hydrogen ions into the mitochondrion.
The Goldman–Hodgkin–Katz voltage equation, sometimes called the Goldman equation, is used in cell membrane physiology to determine the resting potential across a cell's membrane, taking into account all of the ions that are permeant through that membrane.
Notably, DmUCP4A has been shown to protect against mitochondrial dysfunction in Parkinson's disease models by increasing mitochondrial membrane potential and ATP synthesis. Recent studies have demonstrated that DmUCP4A functions as an aspartate transporter, facilitating the unidirectional movement of aspartate from mitochondria to the cytosol.
The energy transferred by electrons flowing through this electron transport chain is used to transport protons across the inner mitochondrial membrane, in a process called electron transport. This generates potential energy in the form of a pH gradient and the resulting electrical potential across this membrane.
The relationship of these parameters can be expressed by an equation solving for the 'reversal potential of the ANT" (Erev_ANT), a value of the mitochondrial membrane potential at which no net transport of adenine nucleotides takes place by the ANT. [14] [15] [16] The ANT and the F0-F1 ATP synthase are not necessarily in directional synchrony. [14]