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Key Review Points: 1. Electrical signaling depends on the motion of ions across neuronal membranes 2. Na + , K + , Cl - and Ca ++ ions are distributed unequally across neuronal membranes 3. At rest, diffusion of these ions creates the membrane potential 4. Rapid changes in ionic permeability cause transient, self-regenerating changes in the membrane potential known as action potentials, which

Key Review Points:

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Key Review Points: 1. Electrical signaling depends on the motion of ions across neuronal membranes 2. Na + , K + , Cl - and Ca ++ ions are distributed unequally across neuronal membranes 3. At rest, diffusion of these ions creates the membrane potential - PowerPoint PPT Presentation

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Page 1: Key Review Points:

Key Review Points:1. Electrical signaling depends on the motion of

ions across neuronal membranes

2. Na+, K+, Cl- and Ca++ ions are distributed unequally across neuronal membranes

3. At rest, diffusion of these ions creates the membrane potential

4. Rapid changes in ionic permeability cause transient, self-regenerating changes in the membrane potential known as action potentials, which carry information

Page 2: Key Review Points:

Today’s Lecture:

Ion channels: proteins that form pores in the membrane to permit ions to cross

Ion transporters: proteins that actively transport ions across membranes to establish concentration gradients

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New technology: The patch clamp technique

The voltage clamp technique shown before was adequate for large currents, but produced large ‘background noise’

‘Patch clamp’ technique has superior signal-to-noise ratio, so very small currents can be measured, even down to the current passed through a single ion channel!

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Early sodium current during the action potential is due to the aggregate action of many individual sodium channels

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Later potassium current during the action potential is due to the aggregate action of many individual potassium channels

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Voltage dependence of open Na+ and K+ channel open probabilities mirrors the voltage dependence of Na+ and K+ conductances

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Voltage-dependent Na+ and K+ channelsGeneral concept

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How can a protein sense voltage?

How does it respond respond with the appropriate timing?

How does it permit some ions to cross the membrane while excluding others?

How does it inactivate?

--> Functional studies of ion channel proteins

General questions about ion channels

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Need to express ion channels in cells, in isolation from other channels:The Xenopus oocyte electrophysiology technique

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Types of ion channels

Further diversity gained through alternative splicing, editing, phosphorylation, mixing and matching of different subunit types

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Functional diversity Example: K+ channels

Nearly 100 known

Examples of functional variations:

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Molecular architecture of ion channels

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X-ray crystallography reveals mechanisms of ion permeation, selectivityKCsA bacterial ion channel

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Geometry of negative charges, pore size, and ion hydration work together to provide K+ selectivity, excluding Na+

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Mechanism of voltage sensitivity

TM4 contains charged residues; these move in the membrane when membrane potential changes

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Human neurological diseases are caused by ion channel mutations

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Kinetic properties of ion channels are finely-tuned, alteration of them causes disease

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Ion transporters:

Proteins that actively transport ions across membranes to establish concentration gradients

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Na+ efflux from the squid giant axon:

Sensitive to removal of extracellular K+

Sensitive to block of intracellular ATP generation

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Usually, the Na+/K+ ATPase has only a small direct effect on membrane potential, (<1 mV) because it is very slow compared to ion flux through ion channels

However, it can have a larger effect if in small-diameter axons, where the ratio of surface-area to cytoplasm volume is small and ion concentrations change appreciably

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Transporter structures

Na+/K+ ATPase, deduced by mutagenesis

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The Ca++ pump: a more structure-based view