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Ch 24 pages 636-643

Lecture 11 – Equilibrium centrifugation. Ch 24 pages 636-643. Summary of Lecture 10. Sedimentation can be used very effectively to separate, purify and analyze all kind of cellular components

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Ch 24 pages 636-643

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  1. Lecture 11 – Equilibrium centrifugation Ch 24 pages 636-643

  2. Summary of Lecture 10 • Sedimentation can be used very effectively to separate, purify and analyze all kind of cellular components • It can be understood using the mechanical analogy with flow under gravitation. The steady state velocity at which a particle move under centrifugation is determined by the balance between the angular velocity at which centrifugation occurs and the opposing buoyancy and frictional forces.

  3. Summary of Lecture 10 • We have introduced the sedimentation coefficient: Its dimensions are sec, but a more convenient unit is the Svedberg: S=10-13 s • Values for s are usually referred to pure water at 293K=20oC. Under these conditions, the sedimentation coefficient is indicated as follows:

  4. Summary of Lecture 10 • A sedimentation coefficient measured under other conditions, i.e. in a buffered aqueous solution b and/or at another temperature T can be related to standard conditions by the equation • Boundary sedimentation is an equilibrium technique that can be used to separate and analyze macromolecules by sedimentation.

  5. Equilibrium Centrifugation A macromolecular solution subjected to a centrifugal field will quickly attain a steady state condition in which transport of solute mass occurs at constant velocity and a concentration gradient will be generated If we spin very fast, eventually the entire macromolecular population will deposit at the bottom of the tube, at a rate that depends on the centrifugal speed and the density and viscosity of the solvent If we do not spin too fast, centrifugation and diffusion will balance each other out so that the system will attain equilibrium, at which point net transport will cease and transport velocity is zero

  6. Equilibrium Centrifugation This is because transport by centrifugation and by diffusion will oppose and balance each other: centrifugation will generate a density gradient, and diffusion will try and eliminate such gradient The rate at which equilibrium is reached depends on kinetic properties (diffusion coefficient, angular velocity etc) The equilibrium state does not The concentration at equilibrium is only determined by thermodynamic properties of the system and not by sedimentation coefficients, diffusion etc

  7. Equilibrium Centrifugation The equilibrium concentration can be derived by considering Boltzmann’s distribution. Let us consider again the analogy with gravitation. Molecules in a gravitational field will have different energy depending on whether they are higher or lower; the distribution of molecules in different energy levels is given by Boltzmann’s expression: The probability ratio is equivalent to the ratio of concentrations; if we express the energy per mole instead of per particle by multiplying by Avogadro’s number, we find:

  8. Equilibrium Centrifugation Let us return to centrifugation; the centrifugal acceleration for a centrifuge spinning with angular speed w is w2r, the force acting on the particle is Therefore, the energy is:

  9. Equilibrium Centrifugation Substituting this expression we immediately find the expression for the concentration as a function of the axial distance r:

  10. Equilibrium Centrifugation Another derivation re-introduces the chemical potential. The condition of equilibrium requires that the free energy, i.e. the system’s chemical potential, which is the sum of the chemical and centrifugal potential, is minimum. If you think about how centrifugation works, what we would like to know is really the concentration profile with respect to the radius r not as a function of time (as in non-equilibrium centrifugation), but rather at equilibrium. We can then impose that the derivative of the chemical potential with respect to r is 0 at equilibrium. In lecture 6,we have introduced the chemical potential in analogy to the classical concept of force as of a potential gradient, to express differences in free energy that induce diffusion

  11. Equilibrium Centrifugation If the concentration of solute C2 is a function of x, the chemical potential has the general form A difference in chemical potential exercises a force on the solute molecules, and the force that induces solute flow is related to the chemical potential by the diffusion equation. In the case of centrifugation, we have to add a term that describes the centrifugal field, so that the total chemical potential of the system is:

  12. Equilibrium Centrifugation Here C is the solute concentration at position r in the centrifuge tube and U is the centrifugal potential at position r in the centrifuge tube. At equilibrium:

  13. Equilibrium Centrifugation We can substitute for dU/dr the expression for the centrifugal force provided in the previous lecture (remember, a force is a gradient of a potential), then multiply by Avogadro’s number to obtain the centrifugal potential per mole of solute (which is what the chemical potential will be expressed in) and equate the derivative of the concentration with the derivative in centrifugal potential to obtain:

  14. Equilibrium Centrifugation Integrating that equation:

  15. Equilibrium Centrifugation Example : Calculate the weight of carboxy-hemoglobin (cHb) using the following data obtained from an equilibrium centrifugation experiment • At r=4.61 cm C(cHb)=1.220 weight % • At r=4.56 cm C(cHb)=1.061 weight % • T=293.3K spinning at 8703 revolutions/minute • The specific volume of cHb is 0.749 cm3/g. • The density of water is 1g/cm3

  16. Equilibrium Centrifugation • At r=4.61 cm C(cHb)=1.220 weight % • At r=4.56 cm C(cHb)=1.061 weight % • T=293.3K spinning at 8703 revolutions/minute • The specific volume of cHb is 0.749 cm3/g. • The density of water is 1g/cm3

  17. Equilibrium Centrifugation This equation means that when a solution reaches equilibrium in a centrifugal field, generated by spinning the sample at an angular frequency w, a concentration gradient will be generated of the shape given above This experiment can be used to measure macromolecular masses or separate components of a mixture A plot of lnC vs. r2is a straight line with slope proportional to M. Notice that this method provides absolute molecular weight, while electrophoresis, for example, only provides relative molecular weights

  18. Equilibrium Centrifugation Example : Consider the centrifugal separation of two gases with molecular weights of 349 g/mole (1) and 352 g/mole (2). How fast do you have to spin the sample to enrich molecule 1 to a level of 1% at r=3cm if its level is 0.7% at r=10cm and T=273K. Set the buoyancy correction to 1 for gases and subtract the two expressions for C2 and C1 to obtain:

  19. Equilibrium Centrifugation Then solve for w2

  20. Equilibrium Sedimentation in a Density Gradient A type of equilibrium centrifugation involves spinning of a concentrated salt solution at very high speed to generate a density gradient (the density of the solution increases with the salt concentration) and has proven very useful in the study of nucleic acids If a macromolecule is also present, it will form a boundary at a point in the salt gradient where the macromolecules are buoyant

  21. Equilibrium Sedimentation in a Density Gradient Suppose a solution of a macromolecule (e.g. DNA) also contains a salt such as CsCl Initially the salt and the DNA have uniform concentrations. Once the centrifugation has commenced, the salt quickly reaches equilibrium; the concentration of CsCl will reach equilibrium as described by the equilibrium centrifugation equation:

  22. Equilibrium Sedimentation in a Density Gradient Because of the equilibrium condition, the density of the solution will vary as a function of r, the distance from the spinning axis. Suppose at r’ the solution has a density where is the specific volume of the macromolecule

  23. Equilibrium Sedimentation in a Density Gradient

  24. Equilibrium Sedimentation in a Density Gradient At r<r’ the density of the solution is less than the DNA “sinks” to the bottom of the tube, being pulled “downward” by the centrifugal force At r>r’ the density of the solution is greater than the DNA ”floats” “upwards” toward the top of the centrifuge At r=r’ the DNA density increases

  25. Equilibrium Sedimentation in a Density Gradient suppose the solution density gradient is roughly linear, with where dr/dr is the density gradient of the solution near r’, and is assumed to be a constant in this region, if we do not go very far from r’

  26. Equilibrium Sedimentation in a Density Gradient Then the condition for equilibrium of the DNA is: If the solution density in the buoyancy correction is the function of r defined above, then:

  27. Equilibrium Sedimentation in a Density Gradient Integrate the equation to find, and after some simple calculus: Although this equation seems similar to the equilibrium centrifugation equation, it has a term (r-r’)2 instead of r2-r’2, so it differs

  28. Equilibrium Sedimentation in a Density Gradient The logarithm can be removed to obtain:

  29. Equilibrium Sedimentation in a Density Gradient This is a gaussian with width: Notice that the standard deviation increases as the salt gradient dr/dr decrease; it also depends on the inverse mass, so that the higher the mass, the sharper the gradient

  30. Equilibrium Sedimentation in a Density Gradient Many macromolecules have buoyant densities sufficiently different that they can be separated by this technique. Hybrid DNA-RNA was discovered using equilibrium centrifugation in a salt gradient, for example, although they differ in mass by very little.

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