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Niels Bohr Institute - Membrane Biophysics Group Nerves: A Physics Problem Thomas Heimburg - Membrane Biophysics Group Niels Bohr Institute, University of Copenhagen 1 Niels Bohr Institute - Membrane Biophysics Group Nerves Luigi Galvani 1737-1798 Hermann v. Helmholtz Archibald V. Hill 1821-1894 1886-1977 Alessandro Volta 1745-1827 Alan L. Hodgkin 1914-1998 Andrew F. Huxley *1917 Ishiji Tasaki *1910 2 Niels Bohr Institute - Membrane Biophysics Group exciting nerves by voltage or currents crayfish motor neuron extracellular mV 0.10 0.05 0.00 -0.05 0.00 0.05 0.10 0.15 time [s] 0.20 0.25 0.30 BUT: Nerves can also be excited by • mechanical means (force) • cooling (temperature) • acids (pH) (These variables were also important for anesthesia) This is so far unexplained and the existing models don‘t address this! 3 Niels Bohr Institute - Membrane Biophysics Group The molecular biology picture of a membrane WHERE IS THE PHYSICS? what about physical variables, e.g.: pressure temperature volume entropy heat length scales time scales ... ? 4 Niels Bohr Institute - Membrane Biophysics Group A physical picture for nerve pulses E. Wilke. 1912. Pflüger‘s Arch. Curtis&Cole. 1942. J. Physiol. Hodgkin & Huxley. 1945. J. Physiol. I want to convince you that nerve pulses are piezoelectric waves (or sound pulses) 5 Niels Bohr Institute - Membrane Biophysics Group reminder: lipid membranes can melt high sensitivity differential micro-calorimetry changes in: • enthalpy: ∆H~35kJ/mol • volume: ∆V/V~0.04 • area: ∆A/A~0.24 !!! • thickness: ∆d/d~ -0.16 6 Niels Bohr Institute - Membrane Biophysics Group Some facts about lipid transitions - last weeks lecture continued The enthalpy (heat uptake) is proportional to the volume and the area: This means that heat is released from the membrane when you compress it The heat capacity cP is proportional to: • • • • volume compressibility area compressibility bending elasticity relaxation times κTV ~ cP κTA ~ cP 1/K = κbend ~ cP τrelax ~ cP This means that membranes are soft in the transition!!! When membranes are compressed they become soft! Heimburg. 1998. Biochim.Biophys.Acta. 1415: 147-162 - Halstenberg et al. 1998. Biophys.J. 75: 264-271 Ebel et al. 2001. J.Phys.Chem.B 105: 7353-7360 - Ivanova et al. 2001. Phys. Rev. E 63: 1914-1925 Grabitz et al., 2002. Biophys.J.82: 299-309 - Schrader et al. 2002. J.Phys.Chem.B 106: 6581-6586 7 Niels Bohr Institute - Membrane Biophysics Group measuring the sound velocity measuring sound velocities in a cavity resonator at 5 MHz: • Sound velocity c c= ! 1 κS · ρ • Sound velocity number u: (normalized sound velocity) c − cH2 O u= cH2 O · [L] one can correctly predict sound velocities from heat capacities Halstenberg,...,Heimburg,Kaatze. 1998. Biophys.J. 75: 264-271 Schrader,..., Heimburg, Kaatze. 2002. J.Phys.Chem.B 106: 6581-6586 8 Niels Bohr Institute - Membrane Biophysics Group some facts about nerves • ion concentrations inside and outside of a nerve are largely different (e.g. squid axon: 400mM K+ inside and 20mM outside, 400mM Na+ outside and 20mM inside) • these concentration differences are responsible for a ‘resting’ potential of the membrane of ~ -70mV (Nernst potential) • electrical excitations called ‘action potentials’ can propagate along nerves (typical velocity 1-100 m/s) • myelinated nerves display faster pulses 9 Niels Bohr Institute - Membrane Biophysics Group Hodgkin-Huxley: equivalent circuits Im dU + gK (U − EK ) + gN a (U − EN a ) + ... = Cm dt currents through membrane, resting potentials for individual ions gK and gNa are the conductivities of the membrane for K+ and Na+, which are typically a function of time and voltage. The currents should produce heat. 10 Niels Bohr Institute - Membrane Biophysics Group Hodgkin-Huxley theory: • It is based on electrical currents through resistors called ion channels • It is not a thermodynamic theory - it does not contain ‘volume’, ‘temperature’, ‘entropy’ etc. as variables - nevertheless, resistors should produce heat with a rate dQ = U · Im > 0 P = dt • The entropy production should always be positive, independent of the direction of the ion flux • Therefore, the action potential must be linked to heat production the Hodgkin-Huxley theory is not (!!!) adiabatic / isentropic 11 Niels Bohr Institute - Membrane Biophysics Group thermodynamics of the nerve pulses • • force exerted by a squid axon during action potential dislocations Iwasa & Tasaki. 1980. BBRC 95: 1328 12 Niels Bohr Institute - Membrane Biophysics Group thermodynamics of the nerve pulses adapted from Ritchie & Keynes, 1985 • heat release and voltage (actually energy of capacitor) are in phase • no net heat release: adiabatic/isentropic! 13 Niels Bohr Institute - Membrane Biophysics Group why is this strange? • • • • the action potential seems to be isentropic (no entropy/heat production) indicating that the physical processes underlying the pulse propagation are reversible processes the mechanical changes are in phase with potential changes the heat changes are in phase with voltage changes the action potential has rather the properties of a pressure wave/ pulse - may the action potential be a sound wave? • • • however: the Hodgkin-Huxley theory is clearly non-isentropic the propagation of the pulse is driven by ion fluxes along gradients (Na+ and K+). It does not contain reversible processes! an isentropic action potential is inconsistent with the HH-theory 14 Niels Bohr Institute - Membrane Biophysics Group sound velocity as function of density c2= 1 =c ρ ⋅ κs € sound velocity Heimburg & Jackson, 2005. PNAS 102: 9790-9795 Interesting spring properties of membranes: • the membrane becomes softer upon compression • frequency dependence of sound velocity nonlinearity dispersion possibility of soliton propagation 15 Niels Bohr Institute - Membrane Biophysics Group soliton in a river 16 Niels Bohr Institute - Membrane Biophysics Group $ % ∂ ∂ ∆ρ ∂ 1 ∆ρ = 2 ∂t ∂x ρ · κS ∂x & '( ) 2 solitons c=const. 2 ∂ 2 ∆ρ ∂ ∆ρ 2 = c0 2 ∂t ∂x2 normal sound propagation c2 2 ∂ ∂ ∆ρ = 2 ∂t ∂x ! " 2 # ∂4 2 ∂ ∆ρ − h 4 c0 + p∆ρ + q∆ρ ∂x ∂x $ DPPC LUV, 45°C width 1 mm for 4 m h=2 2 dispersion s 0.20 v = 0.651 · c0 0.15 ΔρA/ρ0A sound propagation with nonlinearity and dispersion 0.10 0.05 € 0.00 -0.10 -0.05 0.00 z [m] 0.05 0.10 propagation velocity m ≈ 100 s 17 Niels Bohr Institute - Membrane Biophysics Group comparison with experiment real nerve real nerve adapted from Ritchie & Keynes 1985 adapted from Byrne & Tasaki 1981 the properties of our solitons are very similar to those of the nerve pulse Heimburg & Jackson, 2005. Proc.Natl.Acad.Sci. USA102: 9790-9795 18 Niels Bohr Institute - Membrane Biophysics Group advantages of the soliton model • Propagation velocity around 100 m/s - similar than in a myelinated nerve • A soliton would automatically produce heat changes and mechanical displacements in phase with the voltage pulse (action potential) • The model explains why nerve pulses can be induced by cooling or by mechanical perturbations • It also correctly predicts that a nerve pulse can be inhibited by heating • It explains the Meyer-Overton rule and the pressure reversal of anesthesia quantitatively • It also provides a key for the inhibition of anesthesia during inflamation • None of these features are explained by the HH theory 19