Psi Lbr Electrophysiology

7/29/2019 Psi Lbr Electrophysiology

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Paul Scherrer Institut, 5232 Villigen PSI, Schweiz

Telefon +41 56 310 21 11, Telefax +41 56 310 21 99

http://www.psi.ch

Printed from PSI home page

Electrophysiological methods and devicesfor the activity measurement of membrane proteins

Translocation of ions and charged molecules across biological membranes are sensitively measured using

electrophysiological instruments. In principle, an electrical potential is applied across a lipid bilayer membrane and, if

ion channels are open or membrane transporters active, the resulting currents are measured. Membrane resistance in

the Giga-Ohm range of lipid bilayers suspended in micro- or nanopores of the supporting material can be achieved, a

prerequisite for sensitive measurements. Using impedance spectroscopy, the sealing resistance and the total

capacitances of the bilayers and the supporting material are determined. As in patch-clamp measurements (see insert),

voltage pulses can be applied to planar lipid bilayers and opening of ion channels determined as intermediate currents

of some pico Ampres. To measure these low currents, measurements have to be carried out in a Faraday-cage which

shields the measurement cell from outside disturbances.

Instrumentation

Two instruments (Potentiostat Autolab, PG12) are available, equipped with an impedance and a low current

module. Voltage-clamp measurements are carried out using an Axopatch 200 B instrument and a Digidata

1440 A analyser inside a Faraday cage (Warner) .

Rotavap and extruders are used to generate liposomes of uniform sizes.


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Nanopore arrays in a silicon nitride membrane

Suspended bilayer in a nanopore

Instrumental setup for ion channel recording

Transport of solvents in microfluidic systems is achieved by computer-controlled NEMESYS syringe devices.

Materials

Fabrication, derivatization and analysis of micro- and nanopore materials are carried out in collaboration with PSI

Laboratory for micro- and nanotechnolgy and external partners.

Two kinds of materials have been used for bioanalytical devices: silicon and polymers. Silicon technology requires clean

room laboratories including essentially photolithography or e-beam facilities for structure definition and etching processesfor structure generation. Polymers can be structured by hot embossing and molding techniques and surfaces can be

functionalized using chemical methods. Scanning electron microscopy, contact angle measurements and fluorescence

microscopy are methods to analyse surface properties.

Pore generation

In a 300 nm thin silicon nitride membrane on a silicon chip, pores of 200 nm to 25 micrometers have been made. For

ion channel recordings one pore is sufficient, whereas for transporter protein recordings arrays of pores are required.

Since the unitary translocation rate of transporters is about 1000 times lower than that of ion channels, a sufficient

surface density of transporter molecules is required.

The quality of bilayer sealing depends on the lipid composition, the bilayer formation method, the material and the

surface properties (roughness, contact angle). The capacitance mainly depends on the thickness of the supporting

material. If it is thinner than about 10 micrometers, the capacitance values can be hardly compensated to the low values

necessary for Voltage-clamp experiments.

[1]


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Chip i ntegrated in a PDMS microfluidic system

(courtesy NTB)

Polymer-based microfluidic channel with a

micropore (courtesy FHNW, Eugen Mller)

Bilayer formation and protein integration

Microfluidic systems

Fluidic transport to the micrometer-sized pores is tricky. Solvents have to be transported, electrodes integrated and

membrane protein activities of interest measured. Presently emphasis is put on making prototype devices of polymers.

Methods

The integration of membrane proteins into lipid bilayer membranes suspended in micro- or nanopores is a critical step.

Three different strategies (A, B or C) have been evaluated. Pore size, lipid composition and the bilayer formation method,

influence the stability of the planar lipid proteobilayers. Electrophysiological methods are needed to monitor bilayer

formation and to determine membrane-sealing resistance and capacitance of the bilayers formed.

Measuring activities: current traces

Single voltage-gated ion channels are activated by changing the potential from about - 150 mV to + 150 mV. Individual

channels remain open for some ms and the opening and closing of channels can be recorded using the Axopatch


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Current peaks of about 12 pA from single

KvAP ion channels reconstituted in a

DOPG/DOPE bilayer

Membrane proteins having electrogenic

activity

instrument.

Membrane proteins of interest

Using electrophysiological methods, membrane protein mediated translocation of ions across bilayers can be monitored.

Ion channels and transporters are important targets for drugs and thus highly relevant in drug discovery.

For more information Tiefenauer Group Publications and Publications LBR

URLs:

[1] : http://lmn.web.psi.ch/

[2] : http://www.psi.ch/lbr/tiefenauer-group-publications

[3] : http://www.psi.ch/lbr/publications

http://www.psi.ch/lbr/electrophysiology

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Psi Lbr Electrophysiology

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