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From Bioblast
- ...ding outside of the inner mt-membrane or on the outer side of the inner mt-membrane, in contrast to internal unspecific binding. |info=[[Mitochondrial membrane potential]]527 bytes (71 words) - 00:03, 18 February 2020
- ...required to evaluate the necessary limit of detection of TPP<sup>+</sup>, and for restriction of experimental TPP<sup>+</sup> concentrations below the in {{Keywords: Force and membrane potential}}773 bytes (102 words) - 00:03, 18 February 2020
- ...847]]) which cycles across the inner mt-membrane with transport of protons and dissipation of the electrochemical proton gradient. Mild uncoupling may be {{Keywords: Uncoupling}}755 bytes (88 words) - 11:05, 28 March 2024
- ...ometric ion-selective electrodes for measurement of mitochondrial membrane potential ...//www.oroboros.at/index.php/product/o2k-tpp-ise-module/ '''Product details and purchase information''']1,012 bytes (118 words) - 11:49, 17 August 2022
- ...Publications]] [[Instrument and method::Oxygraph-2k]] [[Topic::mt-Membrane potential]] |?Mammal and model=Organism1 KB (184 words) - 00:09, 18 February 2020
- |title=MitoEAGLE preprint 2018-02-18(21) The protonmotive force and respiratory control. ...owing a primary peer-reviewed publication of the concept of stoichiometric potential differences.3 KB (369 words) - 12:48, 23 May 2020
- ...Yildiz Ö, Kühlbrandt W (2017) Structural basis of proton translocation and force generation in mitochondrial ATP synthase. Elife e33274. doi: 10.7554/eLife. ...e steep potential gradient over the sub-nm inter-channel distance exerts a force on the deprotonated glutamate, resulting in net directional rotation.2 KB (220 words) - 17:22, 16 January 2021
- ...u>''e''</u>p<sup>+</sup></sub>, is the electric part of the protonmotive [[force]], Δp = Δ<sub>m</sub>''F''<sub><u>''e''</u>H<sup>+</sup></sub>. ...gy change per ‘motive’ charge or per charge moved across the transmembrane potential difference, with the number of ‘motive’ charges expressed in the unit c6 KB (847 words) - 17:02, 17 January 2024
- ...e=Komlódi T, Tretter L (2022) The protonmotive force – not merely membrane potential. https://doi.org/10.26124/mitofit:2022-0012 — ''2022-11-29 published in [ ...di_2022_MitoFit_Preprints.pdf The protonmotive force - not merely membrane potential] [[File:WatchThePresentationYoutube_icon.jpg|200px|link=https://www.youtube3 KB (405 words) - 16:58, 4 July 2023
- ...e=Komlódi T, Tretter L (2022) The protonmotive force – not merely membrane potential. Bioenerg Commun 2022.16. https://doi.org/10.26124/bec:2022-0016 ...eactive oxygen species production. Measurement of both Δ''Ψ''<sub>mt</sub> and ΔpH allows for calculation of ''pmF''. Methods for monitoring Δ''Ψ''<sub3 KB (410 words) - 07:00, 8 January 2023
- ...i Timea</u>, Tretter L (2022) The protonmotive force – not merely membrane potential. '''Bioblast 2022: BEC Inaugural Conference.''' In: https://doi.org/10.2612 ...ve oxygen species production. Separate measurement of Δ''Ψ''<sub>mt</sub> and ΔpH allows for calculation of ''pmF''. Methods for monitoring Δ''Ψ''<sub3 KB (394 words) - 08:30, 28 July 2022
- |title=Ghelli A, Benelli B, Esposti MD (1997) Measurement of the membrane potential generated by Complex I in submitochondrial particles. J Biochem 121: 746-55 ...complex reducing endogenous ubiquinone (i.e. non-steady-state conditions) and are equivalent to a charge separation similar to that of the antimycin-sens2 KB (254 words) - 16:41, 7 November 2016
- ...the other respiratory chain complexes at different values of protonmotive force occurs by a threshold mechanism. Biochim Biophys Acta 1807: 1114-1124. ...e-mediated threshold-controlled dynamic equilibrium between supercomplexed and isolated states.2 KB (284 words) - 09:56, 8 November 2017
- ...difficult to impossible. Consequently, knowledge of mitochondrial membrane potential is essential to the application of potentiometric fluorophores for the meas ...hydroethidine, dihydroethidium, triphenylphosphonium, superoxide, membrane potential, ROS, Seahorse, respiration, uncoupling2 KB (290 words) - 10:57, 28 September 2018
- ...'ν''<sub>A</sub>=-1/6 in the reaction 0 = -1/6 A - 1 B + 1 C (-1/6 glucose and -1 O<sub>2</sub> converted to +1 H<sub>2</sub>CO<sub>3</sub>). {{Keywords: Force and membrane potential}}704 bytes (112 words) - 05:44, 16 September 2022
- ...969) Estimation of membrane potential and pH difference across the cristae membrane of rat liver mitochondria. Eur J Biochem 7:471-84. ...and the change of these values in the transition from State 5 to States 4 and 3.3 KB (410 words) - 12:16, 28 May 2015
- ...old), Complexes I and III (2.2-fold), ATP production/transport (2.4-fold), and fuel transport/dehydrogenases (1.7-fold). These data support the notion tha |keywords=Metabolic homeostasis, Bioenergetics, Electron transport chain, Cytochrome3 KB (344 words) - 14:19, 13 November 2017
- ...near laws of TIP — implying linear relations between the generalized flows and forces called the ''phenomenological relations'' [2] — must primarily be ...ility of phenomenological coefficients ''L'' non-linearly dependent on the force under simple experimental conditions [3]. This shatters the foundation of t2 KB (312 words) - 21:34, 15 October 2022
- ...is a potential for the movement of protons, and force is a measure of the potential for motion. ...e there is no absolute potential, but isomorphic forces are stoichiometric potential differences<sup>§</sup>.7 KB (1,194 words) - 21:50, 10 July 2022
- ...everse electron transport-associated hydrogen peroxide production in brain and heart mitochondria. J Bioenerg Biomembr 50:355-3653 KB (439 words) - 04:34, 19 July 2022