The Use of Fast Protein Liquid (Size Exclusion) Chromatography for the Fractionation of Crystallins and the Study of β-Crystallin Aggregation
- 1 January 1993
- journal article
- research article
- Published by Taylor & Francis in Journal of Liquid Chromatography
- Vol. 16 (2) , 367-382
- https://doi.org/10.1080/10826079308020919
Abstract
The separation of bovine crystallins on two types of fast protein liquid chromatography® (Pharmacia) size exclusion columns, Superose-6 (fractionation range 5-5.103 kDa) and Superdex-75 (fract. range 3-70 kDa), and on a combination of these was studied. This type of columns combines the biocompatibility of the conventional soft-gels with the performance characteristics of high performance liquid chromatography. Up to 20 mg protein in 100 μl could be separated within two hours on analytical columns without significant loss of resolution. On preparative columns we could fractionate 75 mg of protein within 6 hours. The effect of column load by variation of both concentration and injection volume is reported. It is shown that size estimation of β-crystallins by size exclusion chromatography, as is often done, gives inconsistent results. The possibility that native β-crystallin is significantly larger than sofar assumed cannot be excluded.Keywords
This publication has 20 references indexed in Scilit:
- Rapid separation of bovine β-crystallin subunits βB1, βB2, βB3, βA3 and βA4Experimental Eye Research, 1990
- Evolution of eye lens crystallins: the stress connectionTrends in Biochemical Sciences, 1989
- Structure of the bovine eye lens γs-crystallin gene (formerly βs)Gene, 1989
- Structure and stability of .gamma.-crystallins: tryptophan, tyrosine, and cysteine accessibilityBiochemistry, 1988
- Calf lens α-crystallin quaternary structureJournal of Molecular Biology, 1986
- Structural variation in lens crystallinsTrends in Biochemical Sciences, 1985
- Effects of temperature, concentration and carboxymethylation on interactions of calf lens crystallinsExperimental Eye Research, 1979
- ISOLATION AND PHYSICAL CHARACTERIZATION OF BOVINE LENS CRYSTALLINSInternational Journal of Peptide and Protein Research, 1979
- Effects of sucrose on interactions of calf lens soluble proteinsExperimental Eye Research, 1978
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970