Imagine that you are working with isolated mitochondria and you manage to double the ratio of protons outside to protons inside. In order to maintain the overall \(\Delta G\) at its original value (whatever it is), how would you have to change the mitochondria membrane potential?

Short Answer

Expert verified
To maintain the same \(\Delta G\) after doubling the proton ratio outside to inside, the mitochondria membrane potential \(V\) would have to decrease by \( \frac{RT \ln(2)}{ZF}\), with \(R\), \(T\), \(Z\) and \(F\) being the universal gas constant, absolute temperature, charge of the proton, and Faraday's constant, respectively.

Step by step solution

01

Recall the Nernst Equation

The Nernst equation gives the relationship between ion concentrations (here, proton concentrations outside and inside the mitochondria) and membrane potential. It can be written as:\[ \Delta G = RT \ln \left( \frac{[H+]_{outside}}{[H+]_{inside}} \right) - ZFV \]where:\(\Delta G\) is the Gibbs free energy,\(R\) is the universal gas constant,\(T\) is the absolute temperature,\([H+]_{outside}\) and \([H+]_{inside}\) are proton concentrations outside and inside the mitochondria respectively,\(Z\) is the charge of the ion (for protons, this is +1),\(F\) is Faraday's constant, and\(V\) is the membrane potential.
02

Consider the change to the proton ratio

The question states that the ratio of protons outside to inside has doubled. Mathematicallly, this means that the ratio \([H+]_{outside}/[H+]_{inside}\) has changed to \(2([H+]_{outside}/[H+]_{inside})\).
03

Adjust the Nernst Equation to matched the changed ratio

With the modified ratio, the Nernst equation becomes:\[ \Delta G = RT \ln \left( 2 \frac{[H+]_{outside}}{[H+]_{inside}} \right) - ZFV \]This simplifies to:\[ \Delta G = RT \ln(2) + RT \ln\left(\frac{[H+]_{outside}}{[H+]_{inside}}\right) - ZFV \]
04

Calculate the new membrane potential

Since the overall \(\Delta G\) is to remain constant, we adjust \(V\) (the membrane potential) to offset the added term in the equation. Consequently, we subtract \(RT \ln(2)\) from \(ZFV\), and obtain the new potential \(V'\) where:\[ V' = V - \frac{RT \ln(2)}{ZF}\]

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Nernst Equation
The Nernst equation is a fundamental principle in electrophysiology that links the concentration of ions on either side of a membrane to the electric potential across it. Understanding this equation is crucial for uncovering how cells generate and maintain voltage differences across their membranes, which is essential for processes like nerve transmission and muscle contraction.

In the case of mitochondria, the Nernst equation can be employed to determine the membrane potential considering the proton concentrations inside and outside the mitochondria. The equation reflects how the movement of ions across the membrane, specifically protons in this context, can be converted into electrical potential energy. The more significant the difference in the proton concentrations, the greater the electric potential that can be generated. Simply put, it's like considering the difference in height when looking at a waterfall: the greater the height difference, the more potential energy available.

The equation is frequently written as \[ \Delta G = RT \ln \left( \frac{[H^+]_{outside}}{[H^+]_{inside}} \right) - ZFV \]It incorporates constants: 'R' for the universal gas constant, 'T' for temperature in Kelvin, 'F' for Faraday's constant, and 'Z' for the valency number of the ion, which for protons is +1. The term 'V' represents the membrane potential. Proton concentration gradients are key in this equation and directly influence the value of 'V'.
Mitochondria
Mitochondria, often referred to as the powerhouses of the cell, are essential for converting the energy stored in food into a form that cells can use—adenosine triphosphate (ATP). This organelle has a double membrane with the inner one folded into structures called cristae, which increase its surface area for energy production.

Inside mitochondria, a chain of reactions known as the electron transport chain is critical for ATP synthesis. This chain of reactions uses the energy from electrons to pump protons from the mitochondrial matrix to the intermembrane space, creating a proton gradient. The membrane potential, generated as a result of this proton gradient, is then utilized by another protein complex called ATP synthase to produce ATP. The concept of membrane potential is thus crucial to understanding how mitochondria function and power the cell.

As chemical reactions occur within the mitochondria, they have to carefully manage the balance of ions across their membranes to keep generating ATP efficiently. Changes in the proton gradient or membrane potential can have significant effects on the mitochondria's ability to produce energy, demonstrating the tight regulation of these parameters within cellular processes.
Proton Gradient
A proton gradient is a gradient of hydrogen ion concentration across a membrane, such as the inner mitochondrial membrane. This gradient is established by the action of the electron transport chain, which actively transports protons from the mitochondrial matrix to the intermembrane space.

The resulting concentration difference creates both a chemical gradient (difference in solute concentration) and an electrical gradient (difference in charge) across the membrane. Collectively, this manifests as an electrochemical gradient. The proton gradient is the driving force behind the production of ATP in a process known as chemiosmosis. In the exercise, you were tasked with imagining how a doubling of the proton ratio outside to inside the mitochondria affects membrane potential. The proton gradient is pivotal in this consideration as it directly affects the Nernst equation and therefore the membrane potential. This gradient is like a stored battery, a reserve of energy that ATP synthase taps into to synthesize ATP, the currency of cellular energy.
Gibbs Free Energy
Gibbs free energy, denoted as \(\Delta G\), is a thermodynamic quantity that indicates the amount of energy capable of doing work during a process at constant temperature and pressure. It is a central concept in predicting the spontaneity of a chemical reaction. A negative \(\Delta G\) suggests that a reaction is spontaneous, while a positive \(\Delta G\) indicates a non-spontaneous reaction.

In biological systems, \(\Delta G\) is critical for understanding how energy is stored and released. When applied to the membrane potential in mitochondria, it explains the possibility and direction of the flow of protons across the membrane. The relationship between membrane potential, ion gradients, and Gibbs free energy is quantified through the Nernst equation. In our exercise, maintaining the original \(\Delta G\) despite changes in the proton gradient requires an adjustment of the membrane potential. Keeping \(\Delta G\) constant ensures that there is no change in the capacity to do work, such as synthesizing ATP, within the mitochondria.

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

a. What is the standard free energy change \(\left(\Delta G^{\circ}\right)\) for the reduction of coenzyme \(\mathrm{Q}\) by \(\mathrm{NADH}\) as carried out by Complex \(\mathrm{I}\) (NADH-coenzyme Q reductase) of the electron-transport pathway if \(\mathscr{E}_{\mathrm{o}}^{\prime}\left(\mathrm{NAD}^{+} / \mathrm{NADH}\right)=-0.320 \mathrm{V}\) and \(\mathscr{E}_{\mathrm{o}}^{\prime}\left(\mathrm{CoQ} / \mathrm{CoQH}_{2}\right)=\) \(+0.060 \mathrm{V}\) b. What is the equilibrium constant \(\left(K_{\mathrm{eq}}\right)\) for this reaction? c. Assume that (1) the actual free energy release accompanying the NADH- coenzyme Q reductase reaction is equal to the amount released under standard conditions (as calculated in part a \(),(2)\) this energy can be converted into the synthesis of ATP with an efficiency \(=0.75\) (that is, \(75 \%\) of the energy released upon NADH oxidation is captured in ATP synthesis), and (3) the oxidation of 1 equivalent of NADH by coenzyme Q leads to the phosphorylation of 1 equivalent of ATP. Under these conditions, what is the maximum ratio of [ATP]/ \([\mathrm{ADP}]\) attainable by oxidative phosphorylation when \(\left[\mathrm{P}_{\mathrm{i}}\right]=1 \mathrm{m} M ?\) (Assume \(\Delta G^{\circ \prime}\) for ATP synthesis \(=+30.5 \mathrm{kJ} / \mathrm{mol}\).)

A wealthy investor has come to you for advice. She has been approached by a biochemist who seeks financial backing for a company that would market dinitrophenol and dicumarol as weight-loss medications. The biochemist has explained to her that these agents are uncouplers and that they would dissipate metabolic energy as heat. The investor wants to know if you think she should invest in the biochemist's company. How do you respond?

Based on your reading on the \(\mathrm{F}_{1} \mathrm{F}_{0}\) -ATPase, what would you conclude about the mechanism of ATP synthesis: a. The reaction proceeds by nucleophilic substitution via the \(S_{N} 2\) mechanism. b. The reaction proceeds by nucleophilic substitution via the \(\mathrm{S}_{\mathrm{N}} 1\) mechanism. c. The reaction proceeds by electrophilic substitution via the \(\mathrm{E} 1\) mechanism. d. The reaction proceeds by electrophilic substitution via the \(\mathrm{E} 2\) mechanism.

For the following redox reaction, \\[ \mathrm{NAD}^{+}+2 \mathrm{H}^{+}+2 e^{-} \longrightarrow \mathrm{NADH}+\mathrm{H}^{+} \\] suggest an equation (analogous to Equation 20.12 ) that predicts the pH dependence of this reaction, and calculate the reduction potential for this reaction at \(\mathrm{pH} 8\)

In the course of events triggering apoptosis, a fatty acid chain of cardiolipin undergoes peroxidation to release the associated cytochrome \(c .\) Lipid peroxidation occurs at a double bond. Suggest a mechanism for the reaction of hydrogen peroxide with an unsaturation in a lipid chain, and identify a likely product of the reaction.

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free