Sodium-Potassium Pump Calculator
Calculate Resting Membrane Potential and Pump Contributions
Enter ion concentrations (mM) and relative permeabilities to estimate the resting membrane potential using the Goldman-Hodgkin-Katz equation. The calculator also shows individual equilibrium potentials (Nernst) and the direct electrogenic contribution of the Na+/K+ pump (~ -10 mV).
About the Sodium-Potassium Pump Calculator
The Sodium-Potassium Pump Calculator is an educational tool designed to illustrate the critical role of the Na⁺/K⁺-ATPase (sodium-potassium pump) in maintaining cellular ion gradients and the resting membrane potential. This pump actively transports three sodium ions out of the cell and two potassium ions into the cell per ATP hydrolyzed, establishing the electrochemical gradients essential for nerve impulses, muscle contraction, nutrient uptake, and overall cellular homeostasis.
Using peer-reviewed biophysical principles, this calculator computes equilibrium potentials via the Nernst equation and the resting membrane potential via the Goldman-Hodgkin-Katz (GHK) equation, while highlighting the pump's direct electrogenic contribution.
Importance of the Sodium-Potassium Pump
The sodium-potassium pump is fundamental to life, consuming up to 30-70% of cellular ATP in neurons. It maintains low intracellular Na⁺ and high intracellular K⁺, creating gradients that drive secondary active transport (e.g., glucose uptake via SGLT) and enable rapid repolarization during action potentials.
Disruptions in pump function lead to cellular swelling, impaired excitability, and diseases like heart failure (targeted by digitalis drugs) or neurological disorders. In kidneys, it powers reabsorption; in neurons, it supports signaling.
Scientific Basis of the Calculator
The calculations are based on established formulas:
- Nernst Equation: E_ion = (RT/zF) × ln([ion]_out/[ion]_in) – simplified to ~61 × log₁₀([ion]_out/[ion]_in) mV at 37°C for monovalent ions.
- Goldman-Hodgkin-Katz Equation: Accounts for multiple ions and their permeabilities to predict resting potential.
- Pump Stoichiometry: 3 Na⁺ out : 2 K⁺ in : 1 ATP, net export of +1 charge/cycle (electrogenic, contributing ~ -10 mV).
- References include classic works (Hodgkin-Huxley, Skou's Nobel-winning discovery) and Wikipedia's entry on Sodium-Potassium Pump.
User Guidelines
1. Use typical mammalian values (provided as defaults) for accurate estimates.
2. Permeabilities are relative to P_K=1; adjust for different cell types (e.g., higher P_Na in excited states).
3. Results are educational; real cells include other ions and dynamic regulation.
4. Temperature assumed 37°C.
When and Why You Should Use This Tool
Use this calculator when studying neurophysiology, cell biology, or pharmacology. It demonstrates how ion gradients drive membrane potential and why pump inhibition (e.g., by ouabain) depolarizes cells. Ideal for visualizing effects of hyperkalemia or hyponatremia on excitability.
Purpose of the Sodium-Potassium Pump Calculator
This tool educates on the pump's role in the fluid mosaic model and electrochemical driving forces. It shows why the resting potential (~ -70 mV) is close to E_K (~ -90 mV) due to high K⁺ permeability.
The pump's cycle involves conformational changes (E1/E2 states), phosphorylation, and ion occlusion. Its electrogenicity adds a small hyperpolarizing current.
In evolution, the 3:2 ratio optimizes energy use against gradients. In pathology, mutations cause neurological diseases; therapeutically, cardiac glycosides inhibit it to increase contractility.
Experimental validation includes patch-clamp, fluorescence, and crystallography (PDB structures).
For deeper reading, see the Sodium-Potassium Pump Wikipedia page or physiology textbooks.
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The sodium-potassium pump, discovered by Jens Christian Skou (Nobel Prize 1997), is a P-type ATPase. It alternates between E1 (cytoplasm-open) and E2 (extracellular-open) conformations.
In E1, high-affinity Na⁺ sites bind 3 Na⁺; ATP phosphorylates Asp369, occluding Na⁺ and flipping to E2-P, releasing Na⁺ outside.
Then, 2 K⁺ bind low-affinity sites, dephosphorylating the pump and returning to E1, releasing K⁺ inside.
This cycle counters passive leaks, maintaining gradients despite channels.
In neurons, it enables action potentials: Na⁺ influx depolarizes, K⁺ efflux repolarizes, pump restores gradients.
Energy cost: ΔG_ATP ≈ -50 kJ/mol under cellular conditions, sufficient for gradients.
Regulation: hormones (insulin stimulates), isoforms (α1 ubiquitous, α3 neuronal).
In plants/fungi, similar H⁺-ATPases; animals uniquely use Na⁺/K⁺.
This calculator simplifies these principles interactively, promoting understanding of cellular electrochemistry.











