Transfer of charged molecules [Na + ](2) [Cl - ](2)  2 [Na + ](1) [Cl - ](1)  1 Electrical Potential (  ) Position (x) 11 22 Electric field does work on ion as it passes between solutions.  µ A = µ A (solution 2) - µ A (solution 1) + ZFV V = (  2 -  1 ) potential difference in volts between the two solutions. F = Faraday = 96,485 (eV -1 ) = charge of mole of electrons. Z = charge of the ion (e.g. ±1 ) Note: this is true for any  (x). Convenient to write: µ A,tot = µ A + ZF 

Electrostatics in Water Charged surface  = charge density Counter charges (in solution) Potential  Chemical potentials of molecules on the surface are influenced by the surface potential, .  = f(  )

Gouy-Chapman Theory Potential  LDLD

Surface Potential Potential  LDLD Gouy Equation 

Linearized Poisson-Boltzmann Equation Potential  LDLD Good for  0 ≤ 25 mV 

Mobility and Chemical Potential Molecular motion and transport disucssed in TSWP Ch. 6. We can address this using chemical potentials. Consider electrophoresis: –We apply an electric field to a charged molecule in water. –The molecule experiences a force (F = qE) –It moves with a constant velocity (drift velocity = u) It obtains a speed such that the drag exactly opposes the electrophoretic force. No acceleration = steady motion. –u = qE·1/fwhere f is a frictional coefficient with units of kg s -1. qE is a force with units of kg m s -2 giving u with the expected ms -1 velocity units. –Think of (1/f) as a mobility coefficient, sometimes written as µ. –u = mobility · force –We can determine the mobility by applying known force (qE) and measuring the drift velocity, u.

Gradient of the chemical potential is a force. Think about gradient of electrical potential energy: Extending this to the total chemical potential: –where f is a frictional coefficient –(1/f) as a mobility coefficient Mobility and Chemical Potential

Mobility and Chemical Potential: Example E Potential (  ) Position (x) Write down chemical potential as a function of position in this electrophoresis: If concentration (c) is constant througout: And the drift velocity is What if c is not constant? Can the entropy term give rise to an effective force that drives motion? This is diffusion, and we can derive Fick’s Law (TSWP p. 269) from chemical potentials in this way.

Equilibrium Dialysis Example H 2 O (l) O 2 (aq), N 2 (aq) etc. H 2 O (l) O 2 (aq), N 2 (aq) Mb(aq), Mb·O 2 (aq) Semipermeable membrane (cellulose): allows water and dissolved small solutes to pass, blocks passage of large proteins such as myoglobin (Mb) At equilibrium: O 2 (out) = O 2 (in, aq) [Mb·O 2 ]/[Mb][O 2 (aq)] = K eq If we are able to asses the total ligand concentration in the dialysis bag: [O 2 (aq)] + [Mb·O 2 ] = [O 2 (in, total)] Then [Mb·O 2 ] = [O 2 (in, total)] - [O 2 (aq)] (these are measurable) Can compute K eq. If we have direct a probe for Mb·O 2, then we don’t need the dialysis, can read of concentrations and compute K eq. Dialysis can also be used to exchange solution (eg. change [salt])

Scatchard Equation General version: M + A M·A K eq = [M·A]/([M][A]) Simplify by introducing, the average number of ligand molecules (A) bound to the macromolecule (M) at equilibrium: For one ligand binding site per macromolecule Scatchard equation N independent binding sites per macromolecule. /[A] Slope = -K eq N NK eq Scatchard plot

Cooperative Binding For a macromolecule with multiple binding sites, binding to one site can influence binding properties of other sites. Failure of data plotted in a Scatchard plot to give a straight line indicates cooperative or anticooperative binding among binding sites. Cooperative = binding of second ligand is made easier Anticooperative = binding of second ligand is made more difficult Hemoglobin is a favorite example of a protein with cooperative binding behavior.  Binds up to 4 O 2  Cooperative: most O 2 released in tissue while binding O 2 maximally in the lungs  Binding curve shows characteristic sigmoidal shape f 0 1 P O2 (Torr) 0 40 p50 = 16.6 Torr Hemoglobin Myoglobin p50 = 1.5 Torr f = fraction of sites bound

Hill Plot Scatchard equation (non-cooperative binding) For cooperative binding. n = Hill coefficient K = a constant, not the K eq for a single ligand Slope of each line give the Hill cooperativity coefficient. Slope = 1no cooperativity Slope = Nmaximum (all-or-nothing) cooperativity See Example 5.4 (TSWP p ) for a detailed study of Hemoglobin log[P 02 ] (Torr) log[f /(1-f)] Hemoglobin n = 2.8 Myoglobin n = 1.0