Cadmium is discussed as being involved in the development of transitional cell carcinoma (TCC) of the bladder and can be observed in urine of these patients. Investigations of urinary samples from bladder cancer patients and normal controls were carried out with special emphasis on metallothionein (MT)-bound cadmium. Compounds that are constituents of urine were separated in urine samples by means of size exclusion chromatography and cadmium was monitored continuously with a hyphenated inductively coupled plasma mass spectrometry (ICP-MS) system. MT-bound cadmium was quantified by peak area integration, taking into account the intensity of the rhodium signal which was added continuously before ICP-MS detection. The obtained results show that urinary cadmium is predominantly bound to the observed MT-fraction. The median of the MT-bound cadmium concentration in the control group was found to be 0.8 microgL(-1) whereas the cancer group has a median of 1.8 microgL(-1). The variance of the data in the cancer group is much higher than in the controls. However, the urinary MT-bound cadmium is significantly elevated in the cancer group; odds-ratio test: 7.11 (95% C.I.: 1.89-26.80), taking into account the total protein content. Due to the fact that only one main cadmium-containing fraction was observed, there is no necessity to separate the MT-fraction before cadmium determination in urine samples in future studies.

BACKGROUND:Selenium (Se) is an essential element which is involved in various biological processes in nearly all tissues of animals and human, e.g. protection against oxidative stress in the cardiovascular system, and may play a role in cancer protection. It is incorporated in the proteome in the form of the genetically encoded amino acid selenocysteine, which is the characteristic component of the selenoproteins.MATERIALS AND METHODS:We investigated the expression of the selenoenzyme GPx-2 which is predominantly present in the tissues of the gastrointestinal tract such as the small intestine and therefore named gastrointestinal glutathione peroxidase. Rats were fed with a Se-adequate or Se-deficient diet and GPx-2 was assessed by means of enzyme activity with respect to the Se concentration in tissues of the colon and small intestine. Se quantification was carried out by means of graphite furnace atom absorption spectrometry and 2D-gel electrophoresis was applied to investigate the expression of the proteins of the small intestine tissue samples.RESULTS:Twenty-eight differences could be distinguished in the protein spot distribution of the 2D-gels of the homogenates. The GPx-2 activity in the Se-deficient rat colon samples was 6.8 fold lower than in the Se-adequate rats in contrast to 1.2 fold lower levels between the corresponding samples in the small intestine.CONCLUSION:This finding might explain the different susceptibility of the colon and the small intestine to cancer and support the theory of the protective effect of selenium in the gastrointestinal tract.

For investigations of metalloproteins by speciation analysis, the integrity of the protein–metal complexes before and during separation is crucial. Knowledge about potential alterations of the samples is thus essential to avoid misinterpretations of the analytical results. Chromatographic element profiles of different cytosolic samples from animal tissues were measured repeatedly to estimate the sample stability. The dependence of the signals on the dwell time of the sample in an autosampling device at 4 °C for a period of 10 h was observed. Alterations in the element content of different metal-containing fractions were quantified by means of recovery values. Some metalloprotein fractions (e.g. ≈27-kDa arsenic, ≈27-kDa iron and different zinc fractions) were stable or only minor alterations were observed and for their investigation an autosampling device is therefore suitable. However, most of the other metalloprotein fractions, especially nickel-containing proteins, showed major alterations: these samples should therefore be analysed immediately after preparation or directly after thawing.

In the present studies radiotracer techniques have been combined with biochemical separation procedures to investigate the selenium-containing proteins in the culture cells of the lung, trachea and their subcellular fractions. Subcellular separation of the lung and trachea tissues has been achieved by differential ultracentrifugation. The selenium-containing proteins in these compartments have been investigated by labeling of lung and trachea cultured cells in vitro with Se-75, gel electrophoretic separation of the proteins and autoradiographic detection of the tracer. The protein separation by gel electrophoresis using mono-dimensional (1D)- and two-dimensional (2D)-SDS-PAGE has been successfully applied for the selenium research. It has resulted in the detection of a large number of selenium-containing proteins. Two-dimensional gel electrophoresis (2-DE) was also helpful in the identification of the proteins of interest according to their molecular mass and isoelectric point. In this way more than 30 selenium-containing proteins could be distinguished in the lung and trachea samples. Some of them such as Gpx1, Trx1, SelP, SelT and Sel15 could be identified by means of immunoassays, their molecular weight and pI values and localized in the cellular compartments.

In the human body, there exists over 200 different cell types, which differ in size and structure and have specialised functions in the organism. Therefore it can be assumed that these different cells also contain different proteins necessary to carry out the respective specialised functions. This supposed different metalloprotein composition in different human organs cannot be demonstrated by determination of total element concentrations. Therefore investigations of the different protein-bound forms of the elements were achieved by speciation analysis: The biomolecules were separated by size exclusion chromatography and the elements detected on-line in the eluate by a hyphenated inductively coupled plasma mass spectrometer (ICP-MS). For the interpretation of the obtained element profiles, an identification of the signals and their assignment to different metalloproteins was necessary. This identification was carried out by means of specific protein assays, i.e. enzymatic assays or immunochemical reactions, in collected fractions of the chromatographic separations. A comparison of the element binding pattern in cytosols of different human organs was then possible. The optimised method was applied to tissue cytosols of different human organs. As expected, the element patterns varied for different organs of the same patient and for the same organ of patients with different diseases. Metalloproteins and their bound metals could consequently be considered as biological markers for physiological differences or pathological changes in human tissues.

Capillary zone electrophoresis, with its high resolution capability in the separation of different compounds, is well suited for the investigation of metal-containing proteins, especially when elemental detection is conducted using hyphenated inductively coupled plasma-mass spectrometry. A major problem in the separation of proteins in body fluids is caused by the effects of different sample matrix composition. The migration time of proteins varies significantly, depending on the nature of the matrix. Electropherograms are consequently difficult to compare and the peak identification is uncertain. Pre-analytical steps for the reduction of matrix compounds enhance the quality of the data, but the results are still unsatisfactory. This paper describes a technique for obtaining electropherograms that can be used for comparison purposes by correction of the data with the aid of time markers. A mixture of five substances (caesium chloride, arsenocholine, arsenobetaine, dimethylarsinic acid and monomethylarsonic acid) was added in a separate injection step. Ionic caesium eluted at the start of the separation and the other four markers appeared throughout and at the end of the electropherogram. All electropherograms were normalized to a reference run by recalculation of the time axis using the time markers. The method was applied to the analysis of human brain cytosols. Samples were separated after different pre-treatment steps and were compared, with special emphasis on the detection of the isoform metallothionein-3.

Studies to specify various metalloproteins in cell cytosol of tissues using chromatographic separation methods and plasma mass spectrometry for element detection require a careful step by step sample preparation. These steps involve (i) bioptic sample removal from tissue, (ii) extraction and preparation of the tissue supernatant, (iii) the chromatographic separation of the proteins, and finally (iv) the on-line transfer of the column eluate into the plasma mass spectrometer. Each of the analytical steps has to be carefully monitored to avoid undesired changes in the sample composition which could be caused by enzymatic and/or oxidative processes as well as by external element contamination. This presentation introduces a concept to ensure that environmental element contamination does not occur to bias the analytical results.

A new approach for the speciation of metallothioneins (MT) in human brain cytosols is described. The analysis is performed by application of a newly developed coupling of capillary electrophoresis (CE) with inductively coupled plasma–sector field mass spectrometry (ICP–SFMS). Isoforms of metallothioneins are separated from 30–100 µL sample volumes by CE and the elements Cu, Zn, Cd, and S are detected by use of ICP–SFMS.