Agarose

An agarose gel in tray used for gel electrophoresis

An agarose is a polysaccharide polymer material, generally extracted from seaweed. Agarose is a linear polymer made up of the repeating unit of agarobiose, which is a disaccharide made up of D-galactose and 3,6-anhydro-L-galactopyranose.[1] Agarose is one of the two principal components of agar, and is purified from agar by removing agar's other component, agaropectin.[2]

Agarose is frequently used in molecular biology for the separation of large molecules, especially DNA, by electrophoresis. Slabs of agarose gels (usually 0.7 - 2%) for electrophoresis are readily prepared by pouring the warm, liquid solution into a mold. A wide range of different agaroses, of varying molecular weights and properties are commercially available for this purpose.

Structure

The structure of an agarose polymer.

Agarose is a linear polymer with a molecular weight of about 120,000, consisting of alternating D-galactose and 3,6-anhydro-L-galactopyranose linked by α-(1→3) and β-(1→4) glycosidic bonds. The 3,6-anhydro-L-galactopyranose is an L-galactose with an anhydro bridge between the 3 and 6 positions, although some L-galactose unit in the polymer may not contain the bridge. Some D-galactose and L-galactose units can be methylated, and pyruvate and sulfate are also found in small quantities.[3]

Each agarose chain contains ~800 molecules of galactose, and the agarose polymer chains form helical fibres that aggregate into supercoiled structure with a radius of 20-30 nm.[4] The fibers are quasi-rigid, and have a wide range of length depending on the agarose concentration.[5] When solidified, the fibres form a three-dimensional mesh of channels of diameter ranging from 50 nm to >200 nm depending on the concentration of agarose used - higher concentrations yield lower average pore diameters. The 3-D structure is held together with hydrogen bonds and can therefore be disrupted by heating back to a liquid state.

Properties

Agarose is available as a white powder which dissolves in near-boiling water, and forms a gel when it cools. Agarose exhibits the phenomenon of thermal hysteresis in the liquid-to-gel transition, i.e. it gels and melts at different temperatures. The gelling and melting temperature varies depending on the type of agarose. Standard agaroses derived from Gelidium has a gelling temperature of 34–38 °C (93–100 °F) and a melting temperature of 90–95 °C (194–203 °F), while those derived from Gracilaria, due to its higher methoxy substituents, has a higher gelling temperature of 40–52 °C (104–126 °F) and melting temperature of 85–90 °C (185–194 °F).[6] The melting and gelling temperature may be dependent on the concentration of the gel, particularly at low gel concentration of less than 1%. The gelling and melting temperature is therefore given at a specified concentration.

Natural agarose contains uncharged methyl groups and the extent of methylation is directly proportional to the gelling temperature. Synthetic methylation however have the reverse effect, whereby increased methylation lowers the gelling temperature.[7] A variety of chemically modified agaroses with different melting and gelling temperatures are available; these are often made by hydroxyethylation of agarose.

On standing the agarose gels are prone to syneresis (extrusion of water through the gel surface), but the process is slow enough to not interfere with the use of the gel.[8][9]

Agarose gel can have high gel strength at low concentration, making it suitable as an anticonvection medium for gel electrophoresis. Agarose gels as dilute as 0.15% can form slab for gel electrophoresis.[10] The agarose polymer contains charged groups, in particular pyruvate and sulfate.[7] These negative charged groups can retard the movement of DNA in a process called electroendosmosis (EEO), and low EEO agarose is therefore generally preferred for use in agarose gel electrophoresis of nucleic acids.

Applications

An agarose gel with bands of DNA stained with ethidium bromide and visualized under UV light on a UV Transilluminator.

Agarose is a preferred matrix for work with proteins and nucleic acids as it has a broad range of physical, chemical and thermal stability, and its lower degree of chemical complexity also makes it less likely to interact with biomolecules. Agarose is most commonly used as the medium for analytical scale electrophoretic separation in agarose gel electrophoresis. Gels made from purified agarose have a relatively large pore size, making them useful for separation of large molecules, such as proteins and protein complexes >200 kilodaltons, as well as DNA fragments >100 basepairs. Agarose is also used widely for a number of other applications, for example immunodiffusion and immunoelectrophoresis, as the agarose fibers functions as an anchor for immunocomplexes.

Agarose gel electrophoresis

Agarose gel electrophoresis is the routine method for resolving DNA in the laboratory. Agarose gels have lower resolving power for DNA than acrylamide gels, but they have greater range of separation, and are therefore usually used for DNA fragments of 50-20,000 bp in size, although resolution of over 6 Mb is possible with pulsed field gel electrophoresis (PFGE).[11] It can also be used to separate large protein, and it is the preferred matrix for the gel electrophoresis of particles with effective radii larger than 5-10 nm.[10]

The pore size of the gel affects the size of the DNA that can be sieved. The lower the concentration of the gel, the larger the pore size, and the larger the DNA that can be sieved. However low-concentration gels (0.1 - 0.2%) are fragile and therefore hard to handle, and the electropherosis of large DNA molecules can take several days. The limit of resolution for standard agarose gel electrophoresis is around 750 kb.[11] This limit can be overcome by PFGE, where alternating orthogonal electric fields are applied to the gel. The DNA fragments reorientate themselves when the applied field switches direction, but larger molecules of DNA takes longer to realign themselves when the electric field is altered, while the smaller ones are quicker, and the DNA can therefore be fractionated according to size.

Agarose gels are cast horizontally in a mold, and when set, usually run horizontally in a submarine mode in buffer. The DNA is normally visualized by staining with ethidium bromide and then viewed under UV light, but other methods of staining are available, such as SYBR Green, GelRed, methylene blue, and crystal violet. If the separated DNA fragments are needed for further downstream experiment, they can be cut out from the gel in slices for further manipulation.

Agarose-based gel filtration columns used for protein purification on an AKTA FPLC machine.

Protein purification

Agarose gel matrix is often used for protein purification, for example, in column-based preparative scale separation as in gel filtration chromatography, affinity chromatography and ion exchange chromatography. It is however not used as a continuous gel, rather it is formed into porous beads or resins of varying fineness.[12] These agarose-based beads are generally soft and easily crushed, so they should be used under gravity-flow, low-speed centrifugation, or low-pressure procedures.[13] Agarose is a useful material for chromatography because it does not absorb biomolecules to any significant extent, has good flow properties, and can tolerate extremes of pH and ionic strength as well as high concentration of denaturants.[14] Examples of agarose-based matrix for gel filtration chromatography are Sepharose (cross-linked beaded agarose), WorkBeads 40 SEC, Superose (highly cross-linked beaded agarose), and Superdex (dextran covalently linked to agarose).

For affinity chromatography, beaded agarose is the most commonly-used matrix resin for the attachment of the ligands that bind protein.[15] The ligands are linked covalently through a spacer to activated hydroxyl groups of agarose bead polymer. Proteins of interest can then be selectively bound to the ligands to separate them from other proteins, after which it can be eluted. The agarose beads used are typically of 4% and 6% densities, and are highly porous. They allow protein to flow freely through the beads and bind to the ligands, so they can have a high binding capacity for protein. The resins are generally soft, and although increased cross-linking and chemical hardening of the agarose resins can improve its strength, it may also result in a lower binding capacity for protein.

Solid culture media

Agarose plate may sometimes be used instead of agar for culturing organisms as agar may contain impurities that can affect the growth of the organism or some downstream procedures such as PCR. Agarose is also harder than agar and may therefore be preferable where greater gel strength is necessary, and its lower gelling temperature may prevent causing thermal shock to the organism when the cells are suspended in liquid before gelling. It may be used for the culture of strict autotrophic bacteria, plant protoplast,[16] Caenorhabditis elegans,[17] other organisms and various cell lines.

Motility assays

Agarose is sometimes used instead of agar to measure microorganism motility and mobility. Motile species will be able to migrate, albeit slowly, throughout the porous gel and infiltration rates can then be visualized. The gel's porosity is directly related to the concentration of agar or agarose in the medium, so different concentration gels may be used to assess a cell's swimming, swarming, gliding and twitching motility. Under-agarose cell migration assay may be used to measure chemotaxis and chemokinesis. A layer of agarose gel is placed between a cell population and a chemoattractant. As a concentration gradient develops from the diffusion of the chemoattractant into the gel, various cell populations requiring different stimulation levels to migrate can then be visualized over time using microphotography as they tunnel upward through the gel against gravity along the gradient.

Low melting and gelling temperature agaroses

Agarose may be modified by hydroxyethylation, and this substitution reduces the number of intrastrand hydrogen bonds, resulting in lower melting and setting temperature than standard agaroses.[18] The exact temperature is determined by the degree of substitution, and many available low-melting point (LMP) agarose can remain as a fluid at 30–35 °C (86–95 °F) range. This property allow enzymatic manipulations to be carried out by adding slices of melted gel with DNA of interest, after separation using gel electrophoresis, directly to the reaction mixture. The LMP agarose also contain fewer sulphates which can affect some enzymatic reactions, and is therefore preferably used for some applications. Ultra-low melting/gelling temperature agaroses may gel only at 8–15 °C (46–59 °F).

See also

References

  1. ↑ Agar at lsbu.ac.uk Water Structure and Science
  2. ↑ "Agar". Food and Agricultural Organization of the United Nations.
  3. ↑ Rafael Armisen and Fernando Galatas. "Chapter 1 - Production, Properties and Uses of Agar". Fao.org.
  4. ↑ Tom Maniatis, E. F. Fritsch, and Joseph Sambrook. "Chapter 5, protocol 1". Molecular Cloning - A Laboratory Manual 1. p. 5.4. ISBN 978-0879691363.
  5. ↑ Alistair M. Stephen, Glyn O. Phillips, ed. (2006). Food Polysaccharides and Their Applications. CRC Press. p. 226. ISBN 978-0824759223.
  6. ↑ Workshop on Marine Algae Biotechnology: Summary Report. National Academy Press. 1986. p. 25.
  7. 1 2 "Appendix B: Agarose Physical Chemistry" (PDF). Lonza Group.
  8. ↑ S.E. Hill, David A. Ledward, J.R. Mitchell, eds. (1998). Functional Properties of Food Macromolecules. Springer. p. 149. ISBN 978-0-7514-0421-0.
  9. ↑ Haesun Park, Kinam Park, Waleed S.W. Shalaby (1993). Biodegradable Hydrogels for Drug Delivery. CRC Press. p. 102. ISBN 978-1566760041.
  10. 1 2 Philip Serwer (1983). "Agarose gels: Properties and use for electrophoresis". Electrophoresis 4 (6): 375–382. doi:10.1002/elps.1150040602.
  11. 1 2 Tom Maniatis, E. F. Fritsch, and Joseph Sambrook. "Chapter 5, protocol 1". Molecular Cloning - A Laboratory Manual 1. p. 5.2–5.3. ISBN 978-0879691363.
  12. ↑ David Freifelder (1982). Physical Biochemistry: Applications to Biochemistry and Molecular Biology (2nd ed.). WH Freeman. p. 240. ISBN 978-0716714446.
  13. ↑ "Overview of Affinity Purification". Thermo Scientific.
  14. ↑ David Freifelder (1982). Physical Biochemistry: Applications to Biochemistry and Molecular Biology (2nd ed.). WH Freeman. p. 258. ISBN 978-0716714446.
  15. ↑ Pedro Cuatrecasas, Meir Wilchek (2004). William J. Lennarz, M. Daniel Lane, ed. Encyclopedia of Biological Chemistry. Volume 1. Academic Press. p. 52. ISBN 9780124437104.
  16. ↑ J.M. Bonga, Patrick von Aderkas (1992). In Vitro Culture of Trees. Springer. p. 16. ISBN 978-0792315407.
  17. ↑ Guy A. Caldwell, Shelli N. Williams, Kim A. Caldwell (2006). Integrated Genomics: A Discovery-Based Laboratory Course. Wiley. pp. 94–95. ISBN 978-0470095027.
  18. ↑ Tom Maniatis, E. F. Fritsch, and Joseph Sambrook. "Chapter 5, protocol 6". Molecular Cloning - A Laboratory Manual 1. p. 5.29. ISBN 978-0879695774.
This article is issued from Wikipedia - version of the Monday, January 19, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.