Fast Protein Liquid Chromatography
High-resolution protein separation techniques critically depend on the availability of column packings of small average particle size. This gives a minimum of peak broadening on the column owing to the direct relationship between the theoretical plate height parameter, H, and particle size (lowest values of H give the highest resolution). High-performance liquid chromatography (HPLC) procedures exploit column packings with average diameters of as small as 5–40 μm. However, these are used in high-pressure systems (up to 400 bar) often with organic solvents and are generally limited to rather low sample loadings (1). To provide a more biocompatible high-resolution separation of biopolymers, including (although not exclusive to) proteins, Pharmacia (Uppsala, Sweden; now known as, Amersham Biosciences) developed fast protein liquid chromatography (FPLC) in 1982 (2). More recently, Regnier and his colleagues developed “perfusive” packings that contain large through-pores (3). These allow high-resolution chromatography with ion-exchange groups similar to those of Amersham Biosciences columns but at much faster flow rates, giving remarkably short separation times (e.g., 5–7 min). Perfusion chromatography columns are also compatible with the FPLC system.
KeywordsCellulose HPLC Filtration Urea Fractionation
- 1.Boyer, R. F. (1993) Separation and purification of biomolecules by chromatography, in Modern Experimental Biochemistry, Benjamin-Cummings, Redwood City, CA, pp. 90–102.Google Scholar
- 2.Richey, J. (1982) FPLC: a comprehensive separation technique for biopolymers. Am. Lab. 14, 104–129.Google Scholar