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Abstract
Post-translational modifications of lens proteins play a crucial role in the formation of cataract during ageing. The aim of our study was to analyze protein composition of the cataractous lenses by electrophoretic and high-performance liquid chromatographic (HPLC) methods.
Samples were obtained after extracapsular cataract surgery performed by phacoemulsification technique from cataract patients with type 2 diabetes mellitus (DM CAT, n = 22) and cataract patients without diabetes (non-DM CAT, n = 20), while non-diabetic non-cataractous lenses obtained from cadaver eyes served as controls (CONTR, n = 17). Lens fragments were derived from the surgical medium by centrifugation. Samples were homogenized in a buffered medium containing protease inhibitor. Soluble and insoluble protein fractions were separated by centrifugation. The electrophoretic studies were performed according to Laemmli on equal amounts of proteins and were followed by silver intensification. Oxidized amino acid and Phe content of the samples were also analyzed by HPLC following acid hydrolysis of proteins.
Our results showed that soluble proteins represented a significantly lower portion of the total protein content in cataractous lenses in comparison with the control group (CONTR, 71.25%; non-DM CAT, 32.00%; DM CAT, 33.15%; p < 0.05 vs CONTR for both). Among the proteins, the crystallin-like proteins with low-molecular weight can be found both in the soluble and insoluble fractions, and high-molecular weight aggregates were found mainly in the total homogenates. In our HPLC analysis, oxidatively modified derivatives of phenylalanine were detected in cataractous samples. We found higher levels of m-Tyr, o-Tyr and DOPA in the total homogenates of cataractous samples compared to the supernatants. In all three groups, the median Phe/protein ratio of the total homogenates was also higher than that of the supernatants (total homogenates vs supernatants, in the CONTR group 1102 vs 633 μmol/g, in the DM CAT group 1187 vs 382 μmol/g and in the non-DM CAT group 967 vs 252 μmol/g; p < 0.05 for all).
In our study we found that oxidized amino acids accumulate in cataractous lenses, regardless of the origin of the cataract. The accumulation of the oxidized amino acids probably results from oxidation of Phe residues of the non-water soluble lens proteins. We found the presence of high-molecular weight protein aggregates in cataractous total homogenates, and a decrease of protein concentration in the water-soluble phase of cataractous lenses. The oxidation of lens proteins and the oxidative modification of Phe residues in key positions may lead to an altered interaction between protein and water molecules and thus contribute to lens opacification.
| Abbreviations | ||
| ATP | = | adenosine triphosphate |
| AUC | = | area-under-the-curve |
| CBB | = | Coomassie brillant blue |
| CONTR | = | group of control subjects |
| DM | = | diabetes mellitus |
| DM CAT | = | group of cataract patients with type 2 diabetes mellitus |
| DOPA | = | 3-, 4-dihydroxy-phenylalanine |
| EDTA | = | ethylenediamine-tetraacetic acid |
| EGTA | = | ethylene glycol-bis(2-aminoethylether)-tetraacetic acid |
| ELFO | = | electrophoresis |
| Hb A1c | = | hemoglobin A1c |
| HPLC | = | high performance liquid chromatography |
| m-Tyr | = | meta-tyrosine |
| non-DM CAT | = | group of cataract patients without diabetes mellitus |
| o-Tyr | = | ortho-tyrosine |
| p-Tyr | = | para-tyrosine |
| PAGE | = | polyacrylamide gel-electrophoresis |
| Phe | = | phenylalanine |
| PMSF | = | phenylmethanesulfonyl fluoride |
| SDS | = | sodium dodecylsulphate |
| Tyr | = | tyrosine |
| UV | = | ultraviolet |
| Abbreviations | ||
| ATP | = | adenosine triphosphate |
| AUC | = | area-under-the-curve |
| CBB | = | Coomassie brillant blue |
| CONTR | = | group of control subjects |
| DM | = | diabetes mellitus |
| DM CAT | = | group of cataract patients with type 2 diabetes mellitus |
| DOPA | = | 3-, 4-dihydroxy-phenylalanine |
| EDTA | = | ethylenediamine-tetraacetic acid |
| EGTA | = | ethylene glycol-bis(2-aminoethylether)-tetraacetic acid |
| ELFO | = | electrophoresis |
| Hb A1c | = | hemoglobin A1c |
| HPLC | = | high performance liquid chromatography |
| m-Tyr | = | meta-tyrosine |
| non-DM CAT | = | group of cataract patients without diabetes mellitus |
| o-Tyr | = | ortho-tyrosine |
| p-Tyr | = | para-tyrosine |
| PAGE | = | polyacrylamide gel-electrophoresis |
| Phe | = | phenylalanine |
| PMSF | = | phenylmethanesulfonyl fluoride |
| SDS | = | sodium dodecylsulphate |
| Tyr | = | tyrosine |
| UV | = | ultraviolet |