LEARNING OBJECTIVES 1. Overall objectives - Principles that underlie different electrical recording...

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LEARNING OBJECTIVES 1. Overall objectives - Principles that underlie different electrical recording techniques - Physiological and biophysical information the techniques provide 2. Extracellular recording and multi-electrode arrays - spiking (all-or-none) information, neural codes conveyed by individual neurons and by groups of neurons 3. Intracellular recording - measurements of input resistance, synaptic input, and synaptic integration 4. Patch-clamp recording (cell-attached; whole-cell; inside-out patch; outside-out patch) Biophysics 6702 Patch Clamp Technique Stuart Mangel, Ph.D.

Transcript of LEARNING OBJECTIVES 1. Overall objectives - Principles that underlie different electrical recording...

Page 1: LEARNING OBJECTIVES 1. Overall objectives - Principles that underlie different electrical recording techniques - Physiological and biophysical information.

LEARNING OBJECTIVES

1. Overall objectives- Principles that underlie different electrical recording techniques- Physiological and biophysical information the techniques provide

2. Extracellular recording and multi-electrode arrays - spiking (all-or-none) information, neural codes conveyed by individual

neurons and by groups of neurons

3. Intracellular recording - measurements of input resistance, synaptic input, and synaptic integration

4. Patch-clamp recording (cell-attached; whole-cell; inside-out patch; outside-out patch) - measurements of input resistance, synaptic input, synaptic integration;

characteristics of voltage-gated ion channels and single ion channel events

Biophysics 6702 Patch Clamp TechniquesStuart Mangel, Ph.D.

Page 2: LEARNING OBJECTIVES 1. Overall objectives - Principles that underlie different electrical recording techniques - Physiological and biophysical information.

EXTRACELLULAR VS. INTRACELLULAR RECORDING

Extracellularly and intracellularly recorded voltages are in the microvolt and millivolt ranges, respectively.

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Maintaining the resting membrane potential

Vm = lnRTF

pK[K+]o + pNa[Na+]o + pCl[Cl-]i

pK[K+]i + pNa[Na+]i + pCl[Cl-]o

The Goldman-Hodgkin-Katz (GHK) Equation:The steady state membrane potential for a given set of ionic concentrations inside and outside the cell and the relative permeability of the membrane to each ion

extracellular

intracellular

ENa = +56Na+ (150)

EK = -102K+ (3)

ECl = -76Cl- (120)

ECa = +125Ca2+ (1.2)

Na+ (18) K+ (135) Cl- (7) Ca2+ (0.1 µM)Na+,K+-ATPase

-60 to -75 mVNSCC

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Measuring EM

• Measure the potential difference between two electrodes using a D.C. amplifier

• Expected value of the membrane potential is in millivolts (not microvolts), so the gain does not need to be as high

INTRACELLULAR RECORDING

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Intracellular Recording

• When a fine-tipped electrode penetrates the membrane of a cell, one observes a sudden change in the measured potential to a more negative value.

• Typical problems– High impedance μE– Damage when cell

penetrated

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Wheatstone Bridge

• Used to measure an unknown resistance

• Discovered by Hunter Christie, 1833

• Popularized by Charles Wheatstone

MEASURING THE INPUT RESISTANCE

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BALANCING THE BRIDGE

• R1 = Fixed R• R2 = Variable R• R3 = Fixed R• R4 = Unknown R

?

To get R2/R1 = R4/R3,

adjust R2, so that there is

no current across B, CR4 = (R2/R1)·R3

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CALCULATING THE INPUT RESISTANCE OF A CELL

• Balance the bridge before entering the cell

• After impaling the cell,

the bridge is “out of balance” by the R value of the cell

• I is known, measure V, and calculate R using Ohm’s Law (V = IR)

• R = V/I

0 100 200 300 400 500-100

-80

-60

-40

-20

0

Mem

bran

e P

oten

tial (

mV

)

Time (Arbitrary Units)

APPLY DRUG

“Balanced” “Out of Balance”

Did R increase or decrease?

Did channels open or close?

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PATCH-CLAMP RECORDING

• Neher and Sakmann, Nobel Prize, 1991• Tremendous technical breakthrough that improved the signal

to noise ratio of electrical recordings• Record from whole cells or from a small patch of cell

membrane, so only a few ion channels (or one) can be studied• High resistance (in giga-ohms) and high mechanical strength

of the seal between the glass electrode and the cell membrane enable one to observe very small currents.

• The diameter of the tip of patch electrodes can be larger than that of fine-tipped intracellular microelectrodes (1.0 micron vs. 0.05 microns), so that the resistance of patch electrodes is lower (e.g. 5 MΩ vs 200 MΩ). The lower resistance of patch electrodes makes voltage clamping easier.

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Patch clamp recording configurations

Electrode

Glass pipette

Ion channel

Plasma membrane

Cell-attached

Inside-out Outside-out

Whole-cellsuction

pull pull

Perforated-patch antibiotics

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SUMMARY OF ADVANTAGES AND DISADVANTAGES OF PATCH CLAMP CONFIGURATIONS

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THE VOLTAGE CLAMP

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THE ACTION POTENTIAL

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Voltage clamping reveals the ionic currents that underlie the action potentials observed in squid axons

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Activation and Inactivation PropertiesIonic Selectivity

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Reversal potentials for synaptic currents

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Inhibitory actions of GABA synapses result from the opening of ion channels

selective for Cl-

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SODIUM CHANNEL CURRENTS RECORDED FROM CELL-ATTACHED PATCH

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Properties of ACh-gated channels

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Single open ACh-gated channels behave as simple resistors.

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Extracellular Mg2+ ions block NMDA channels under physiological conditions.

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SUMMARY OF ADVANTAGES AND DISADVANTAGES OF PATCH CLAMP CONFIGURATIONS

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Questions:

Stuart Mangel, Ph.D.ProfessorDepartment of Neuroscience The Ohio State UniversityCollege of [email protected]

Readings:Kandel, Schwartz et al., Principles of Neural Science, 2013, 5th Ed., Chap. 7, 9, 10

Squire, Berg et al., Fundamental Neuroscience, 2008, 3rd Ed., Chap. 6, 11