The ultracentrifuge is a centrifuge optimized for spinning a rotor at very high speeds, capable of generating acceleration as high as 1000000 g (approx. 9800 km/s²).[1] There are two kinds of ultracentrifuges, the preparative and the analytical ultracentrifuge. Both classes of instruments find important uses in molecular biology, biochemistry, and polymer science.[2]


In 1924 Theodor Svedberg built a centrifuge capable of generating 7,000 g (at 12,000 rpm), and called it the ultracentrifuge, to juxtapose it with the Ultramicroscope that had been developed previously. In 1925-1926 Svedberg constructed a new ultracentrifuge that permitted fields up to 100,000 g (42,000 rpm)[3]. Modern ultracentrifuges are typically classified as allowing greater than 100,000 g [4]. Svedberg won the Nobel Prize in Chemistry in 1926 for his research on colloids and proteins using the ultracentrifuge [5][6][7].

The vacuum ultracentrifuge was invented by Edward Greydon Pickels in the Physics Department at the University of Virginia. It was his contribution of the vacuum which allowed a reduction in friction generated at high speeds. Vacuum systems also enabled the maintenance of constant temperature across the sample, eliminating convection currents that interfered with the interpretation of sedimentation results.[8]

In 1946, Pickels cofounded Spinco (Specialized Instruments Corp.) to market analytical and preparative ultracentrifuges based on his design. Pickels considered his design to be too complicated for commercial use and developed a more easily operated, “foolproof” version. But even with the enhanced design, sales of analytical centrifuges remained low, and Spinco almost went bankrupt. The company survived by concentrating on sales of preparative ultracentrifuge models, which were becoming popular as workhorses in biomedical laboratories.[8] In 1949, Spinco introduced the Model L, the first preparative ultracentrifuge to reach a maximum speed of 40,000 rpm. In 1954, Beckman Instruments (later Beckman Coulter) purchased the company, forming the basis of its Spinco centrifuge division.[9]

Analytical ultracentrifuge

In an analytical ultracentrifuge, a sample being spun can be monitored in real time through an optical detection system, using ultraviolet light absorption and/or interference optical refractive index sensitive system. This allows the operator to observe the evolution of the sample concentration versus the axis of rotation profile as a result of the applied centrifugal field. With modern instrumentation, these observations are electronically digitized and stored for further mathematical analysis. Two kinds of experiments are commonly performed on these instruments: sedimentation velocity experiments and sedimentation equilibrium experiments.

Sedimentation velocity experiments aim to interpret the entire time-course of sedimentation, and report on the shape and molar mass of the dissolved macromolecules, as well as their size-distribution.[11] The size resolution of this method scales approximately with the square of the particle radii, and by adjusting the rotor speed of the experiment size-ranges from 100 Da to 10 GDa can be covered. Sedimentation velocity experiments can also be used to study reversible chemical equilibria between macromolecular species, by either monitoring the number and molar mass of macromolecular complexes, by gaining information about the complex composition from multi-signal analysis exploiting differences in each components spectroscopic signal, or by following the composition dependence of the sedimentation rates of the macromolecular system, as described in Gilbert-Jenkins theory.

Sedimentation equilibrium experiments are concerned only with the final steady-state of the experiment, where sedimentation is balanced by diffusion opposing the concentration gradients, resulting in a time-independent concentration profile. Sedimentation equilibrium distributions in the centrifugal field are characterized by Boltzmann distributions. This experiment is insensitive to the shape of the macromolecule, and directly reports on the molar mass of the macromolecules and, for chemically reacting mixtures, on chemical equilibrium constants. [12]

The kinds of information that can be obtained from an analytical ultracentrifuge include the gross shape of macromolecules, the conformational changes in macromolecules, and size distributions of macromolecular samples. For macromolecules, such as proteins, that exist in chemical equilibrium with different non-covalent complexes, the number and subunit stoichiometry of the complexes and equilibrium constant constants can be studied.

Analytical ultracentrifugation has recently seen a rise in use because of increased ease of analysis with modern computers and the development of software, including a National Institutes of Health supported software package, SedFit.

Preparative ultracentrifuge

Preparative ultracentrifuges are available with a wide variety of rotors suitable for a great range of experiments. Most rotors are designed to hold tubes that contain the samples. Swinging bucket rotors allow the tubes to hang on hinges so the tubes reorient to the horizontal as the rotor initially accelerates. Fixed angle rotors are made of a single block of material and hold the tubes in cavities bored at a predetermined angle. Zonal rotors are designed to contain a large volume of sample in a single central cavity rather than in tubes. Some zonal rotors are capable of dynamic loading and unloading of samples while the rotor is spinning at high speed.

Preparative rotors are used in biology for pelleting of fine particulate fractions, such as cellular organelles (mitochondria, microsomes, ribosomes) and viruses. They can also be used for gradient separations, in which the tubes are filled from top to bottom with an increasing concentration of a dense substance in solution. Sucrose gradients are typically used for separation of cellular organelles. Gradients of caesium salts are used for separation of nucleic acids. After the sample has spun at high speed for sufficient time to produce the separation, the rotor is allowed to come to a smooth stop and the gradient is gently pumped out of each tube to isolate the separated components.


The tremendous rotational kinetic energy of the rotor in an operating ultracentrifuge makes the catastrophic failure of a spinning rotor a serious concern. Rotors conventionally have been made from high strength-to-weight metals such as aluminum or titanium. The stresses of routine use and harsh chemical solutions eventually cause rotors to deteriorate. Proper use of the instrument and rotors within recommended limits and careful maintenance of rotors to prevent corrosion and to detect deterioration is necessary to mitigate this risk.[13][14]

More recently some rotors have been made of lightweight carbon fiber composite material, which are up to 60% lighter, resulting in faster acceleration/deceleration rates. Carbon fiber composite rotors also are corrosion-resistant, eliminating a major cause of rotor failure.[15]

See also


  1. "Optima MAX-XP". Retrieved 2016-02-20.
  2. Susan R. Mikkelsen & Eduardo Cortón. Bioanalytical Chemistry, Ch. 13. Centrifugation Methods. John Wiley & Sons, Mar 4, 2004, pp. 247-267.
  3. "Svedberg Lecture". Retrieved 2019-02-18.
  4. "Beckman Centrifuges". Retrieved 2019-02-18.
  5. "Svedberg". Retrieved 2010-06-23.
  6. Joe Rosen; Lisa Quinn Gothard. Encyclopedia of Physical Science. Infobase Publishing; 2009. ISBN 978-0-8160-7011-4. p. 77.
  7. "Svedberg Lecture". Retrieved 2019-02-18.
  8. Elzen B. Vacuum ultracentrifuge. In: Encyclopedia of 20th-Century Technology, Colin Hempstead & William Worthington, eds. Routledge, 2005. p. 868.
  9. Arnold O. Beckman: One Hundred Years of Excellence. By Arnold Thackray and Minor Myers, Jr. Philadelphia: Chemical Heritage Foundation, 2000.
  10. "Technical Manual, Spinco Ultracentrifuge Model E". Science History Institute Digital Collections. Retrieved 2018-12-18.
  11. Perez-Ramirez, B. and Steckert, J.J. (2005). Therapeutic Proteins: Methods and Protocols. C.M. Smales and D.C. James, Eds. Volume 308: 301-318. Humana Press Inc, Totowa, NJ.
  12. Ghirlando, R. (2011). "The analysis of macromolecular interactions by sedimentation equilibrium". Modern Analytical Ultracentrifugation: Methods. 58 (1): 145–156. doi:10.1016/j.ymeth.2010.12.005. PMC 3090454. PMID 21167941.
  13. Beckman Instruments, Spinco Division. Urgent corrective action notice: Reclassification to Minimize Ultracentrifuge Chemical Explosion Hazard. June 22, 1984.
  14. Goodman, T. Centrifuge Safety and Security. American Laboratory, February 01, 2007
  15. Piramoon, Sheila. "Carbon fibers boost centrifuge flexibility: advancements in centrifuge rotors over the years have led to improved lab productivity." Laboratory Equipment Mar. 2011: 12+. General Reference Center GOLD. Web. 15 Feb. 2015.
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