Simple Analysis Method for Metallothionein-1, -2 and -3 in the Brain by One-Step Size-Exclusion Column HPLC On-Line Coupling with Inductively Coupled Plasma Mass Spectrometry

Satomi Kameo^1,2*, Kunihiko Nakai³, Akira Naganuma⁴, Hiroshi Koyama² and Hiroshi Satoh¹

¹Environmetal Health Sciences, Tohoku University Graduate School of Medicine, Japan

²Department of Public Health, Gunma University Graduate School of Medicine, Japan

³Development and Environmental Medicine, Tohoku University Graduate School of Medicine, Japan

⁴Laboratory of Molecular and Biochemical Toxicology, Graduate School of Pharmaceutical Sciences, Tohoku University, Japan

*Corresponding Author:

Satomi Kameo
Department of Public Health
Gunma University Graduate School of Medicine
3-39-22 Showa-machi, Maebashi, Gunma 371-8511, Japan
Tel: +81-(0)27-220-8011
Fax: +81-(0)27-220-8016
E-mail: skameo-t@gunma-u.ac.jp

Received date: October 17, 2014; Accepted date: November 14, 2014; Published date: November 18, 2014

Citation: Kameo S, Nakai K, Naganuma A, Koyama H, Satoh H (2014) Simple Analysis Method for Metallothionein-1, -2 and -3 in the Brain by One-Step Size-Exclusion Column HPLC On-Line Coupling with Inductively Coupled Plasma Mass Spectrometry. J Anal Bioanal Tech 5:224. doi: 10.4172/2155-9872.1000224

Copyright: © 2014 Kameo S, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Abstract

A simple analysis method of metallothionein (MT) isoforms MT-1, MT-2, and MT-3 was developed based on the use of one-step size-exclusion column (SEC) HPLC and on-line coupling with inductively coupled plasma mass spectrometry (ICP-MS). For the elucidation of the functions of MT isoforms in the brain, it is necessary to have a simple method to determine these isoforms. A SEC TSK gel G2000 SW_XL PEEK (7.8 mm I.D. × 30 cm) system was used in this study. The HPLC system was connected with a quadrupole ICP-MS. All of the connections were made using PEEK tubing. To induce MTs, cadmium (Cd) chloride was administered to MT-1, 2 null and 129/Sv mice at a dose of 4 mg/kg body weight by i.p. injection. Mice were sacrificed 24 h after treatment under anesthesia. Brains and livers were collected, and all the samples were stored at −80°C until subsequent analyses. Soluble extracts of the livers and brains from 129/Sv mice either treated with cadmium or untreated were analyzed. MT-1, MT-2, and MT-3 were clearly separated by the one-step SEC HPLC-ICP-MS system (monitored at ⁶⁵Cu, ⁶⁶Zn, ¹¹³Cd and 55Mn for element) using an appropriate buffer (25 mM Tris-12.5 mM HCl containing 20 mM KCl) and an ultrafiltration membrane filter to eliminate high molecular weight proteins over 30,000 MW and Cu, Zn-SOD. Retention times (RTs) of peaks of each isoform were distinguishable; RTs of MT-1, MT-2, and rMT-3 were 8.6, 8.1, and 7.6 min, respectively. MT-1, MT-2, and MT-3 were separated clearly using this system. This system would be a powerful tool for the separation and metal-component analysis of MT isoforms to elucidate further the biological functions of MTs in the brain.

Keywords

Metallothionein; MT-3; SOD; HPLC; ICP-MS; Brain

Introduction

Metallothioneins (MTs) are a class of ubiquitously occurring low molecular weight cysteine- and metal-rich proteins containing sulfurbased metal clusters. Mammalian MTs are comprised of four major isoforms designated MT-1 through MT-4. MT-1 and MT-2 are expressed in most tissues, including the brain, whereas MT-3 and MT-4 are expressed predominantly in the central nervous system and in keratinizing epithelia, respectively. MT-1 and MT-2 have been implicated in detoxification of heavy metal poisoning, disparate physiological functions such as zinc and copper metabolism, protection against reactive oxygen species, and adaptation to stress [1-3]. MT-3 was discovered unexpectedly while investigating the hypothesis that in the brains of patients with Alzheimer’s disease (AD) a loss of growth inhibitory factor (GIF) occurs, resulting in unbalanced total neurotrophic activity of the brain [4]. GIF was subsequently isolated from the normal human brain and was shown to belong to the MT family and designated MT-3 [5,6]. MT-3 is a non-inducible protein, primarily found in the brain, and seems to have important neurophysiological and neuromodulatory functions [1,7,8].

High-performance liquid chromatography (HPLC) and capillary electrophoresis (CE) are able to separate different MT isoforms; however, UV detection has relatively poor sensitivity and no metalspecific capabilities [9]. HPLC followed by metal-specific detection using atomic absorption spectrometry (AAS) or inductively coupled plasma atomic emission spectrometry (ICP-AES) was employed for the detection and determination of metal-binding proteins [10,11] as an early hyphenated technique. Recently, inductively coupled plasma mass spectrometry (ICP-MS) has been widely used as a detection tool with hyphenated techniques because of its high sensitivity and multi-element capabilities [9,12-16]. However, in previous studies, no simple system was developed for separating the MT isoforms (MT-1, MT-2, and MT- 3) of brain in one step. Typically, HPLC systems with the combination of two different types of chromatography, such as size-exclusion column chromatography (SEC) and ion-exchange chromatography, or tandem connection with SEC are used.

The applications of various HPLC separation techniques and the coupling to ICP-MS hyphenated techniques are attractive tools and valid alternatives to classical methods for the analysis of MTs. These new techniques have the potential to meet the key challenges in the characterization of MTs [17,18]. In the present study, we developed a simple separation system for analysis of MT-1, MT-2 and MT-3 based on the use of one-step SEC HPLC and on-line coupling with an ICP-MS system with using an appropriate buffer and filter.

Materials and Methods

Animals

MT-1, -2 null mice and 129/Sv mice (as wild type) were purchased from Jackson Laboratory, Bar Harbor, ME, USA. Mice were housed in plastic cages with free access to food and water. The light:dark cycle was 12:12 h and the room temperature was maintained at 21–23°C. The entire procedure was reviewed and approved by the Committees of Animal Experimentation of Tohoku University and Tohoku University School of Medicine.

Chemicals

Cadmium (Cd) chloride and standard solutions of Cd, zinc (Zn), copper (Cu) and manganese (Mn) were products of Wako Pure Chemical Industries, Ltd. (Osaka, Japan). Ultrapure nitric acid was purchased from Kanto Chemicals Co., Inc. (Tokyo, Japan). Trizma base (T1503) and MT-1, -2 standards from rabbit liver (M7641 for metallothionen-1, -2 mixture, M5267 for MT-1, and M5392 for MT- 2) were purchased from Sigma-Aldrich (St. Louis, MO, USA). All other chemicals used were of commercially available analytical grade. Ultrapure water (resistance 18M-Ω/cm) from a Milli-Q Gradient (Millipore, Bedford, MA, USA) was used for all experiments.

Instrumentation: HPLC-ICP-MS

SEC with TSK gel G2000 SW_XL PEEK (7.8 mm I.D. x 30 cm, MW range:5,000-150,000) and a TSK guard column SW_XL PEEK guard column (Tosoh, Tokyo, Japan) for the HPLC system (Nanospace SI- 2, Shiseido, Tokyo, Japan) was used in this study. The HPLC system was connected to a quadrupole ICP-MS system (ELAN5000, Perkin- Elmer, Waltham, MA, USA). All of the connections were made using PEEK tubing to prevent metal-binding absorption to the equipment. Operating conditions for ICP-MS are described in Table 1.

Table 1: Operating conditions for ICP-MS.

Induction of metallothioneins

Cadmium chloride was administered to MT-1, -2 null and 129/Sv (wild type) mice at a dose of 4 mg/kg of body weight by i.p. injection to induce MTs for wild type mice. The mice were sacrificed 24 h after treatment under anesthesia. Untreated control mice also were sacrificed under anesthesia. The brains and livers were collected and all samples were immediately frozen using liquid nitrogen and stored at −80°C until subsequent analyses.

Sample preparation

The experimental protocol for sample preparation of mouse tissues and speciation of metal-binding proteins analyzed by SEC HPLC-ICPMS was as follows. The liver or brain tissue was homogenized in four volumes of 10 mM Tris(hydroxymehyl)aminomethane (Tris)-5 mM HCl using a glass-Teflon homogenizer on ice. The homogenate was centrifuged at 10,000 × g for 1 h at 4°C with a high speed refrigerated microcentrifuge (MX-150 with a TMP-11 rotor, Tomy Seiko Co. Ltd., Tokyo, Japan). The supernatant was divided into two portions. One portion was filtered with an ultrafiltration membrane filter (ultrafree- MC filter, Millipore) by centrifugation at 5,000 × g for 1 h at 4°C. The membrane filter which we used in this study was an ultrafiltration filter to cut the high molecular weight proteins. The cutoff point (Nominal Molecular Weight Limit, NMWL) which we used was 30,000 NMWL. The mechanism of the filter depends on the effects of size exclusion. The other portion was unfiltered. The ultrafiltration membrane-filtered samples or unfiltered samples were subsequently applied to the HPLC column as described below.

Analysis of metal-binding proteins and metallothioneins by SEC HPLC-ICP-MS

An aliquot of 30 μL of the supernatant from the liver or brain tissues of mice either treated with cadmium or untreated was injected into the SEC HPLC system (at a flow rate of 1 mL/min.). Eluates of the supernatants were analyzed by ICP-MS (SEC HPLC-ICP-MS system). As the elution buffer, 25 mM Tris-12.5 mM HCl containing 20 mM KCl was used. The metals in the eluates were continuously monitored at m/z 65(Cu), 66(Zn), 113(Cd) and 55(Mn) for element detection. The peaks of the Cd-complex or Zn, Cu-containing complex detected by HPLC-ICP-MS were confirmed with Sigma-Aldrich rabbit MTs as authentic samples for MT-1 and MT-2. As the MT-3 authentic sample, recombinant MT-3, which we previously produced, was used [19].

Results

Metal-binding proteins and MTs induced by Cd in mouse liver

Figure 1 shows the SEC HPLC-ICP-MS elution profiles of the supernatant from the livers of the Cd-treated 129/Sv mouse. The chromatogram in Figure 1a shows the elution profile of the unfiltered supernatant, and the chromatogram in Figure 1b shows the elution profile of the ultrafiltration membrane filtered supernatant. A SEC gel with a low molecular weight range (5,000-150,000) was chosen to gain clear separation of MT isoforms. In this analysis system, 25 mM Tris- 12.5 mM HCl containing 20 mM KCl was used as the elution buffer. In HPLC-ICP-MS analyses, two major peaks of the Cd complex were detected. The peaks were confirmed using rabbit MTs as authentic samples for MT-1 and MT-2. Several high molecular weight proteins and Cu, Zn-superoxide dismutase (Cu, Zn-SOD; MW 32,000) also were eluted under these conditions (Figure 1a). To remove high molecular weight proteins and Cu, Zn-SOD from the supernatant, an ultrafiltration membrane filter was used before injection of the supernatant into the HPLC column. The resulting elution profile indicated clear separation of MT-1 and MT-2 (Figure 1b). We have also confirmed UV at 254 nm of the samples. Cd-metallothionein (Cd-MT) has a property of a specific absorption at 254 nm based on Cd-thiolate bond. Our results showed also absorptions at 254 nm of MT-1 and MT-2 peaks of SEC HPLC-ICP-MS in Figures 1a and 1b (data not shown). These results supported that the Cd-binding proteins in Figures 1a and 1b were Cd- MT which have many Cd-thiolate bonds.

SEC HPLC-ICP-MS chromatogram of mixture of MT-1, MT- 2, and recombinant MT-3 analyzed by HPLC-ICP-MS

Figure 2 shows an SEC HPLC-ICP-MS chromatogram of a mixture of MT-1 and MT-2 from the ultrafiltration membrane filtered supernatant of the liver of the 129/Sv mouse treated with Cd and recombinant MT-3 (rMT-3). Retention times (RTs) of peaks of each isoform were distinguishable, and RTs of rMT-3, MT-2 and MT-1 were 7.6, 8.1, and 8.6 min, respectively. Thus, MT-1, MT-2, and MT-3 were clearly separated using this system.

Separation of MT-1, MT-2, and MT-3 in the 129/Sv mouse brain (non-Cd treated) analyzed by HPLC-ICP-MS

Figure 3 shows the elution profile of the supernatant from the brain of the 129/Sv mouse (Figure 3a: unfiltered) and elution profile of the ultrafiltration membrane filtered supernatant from the brain of the same mouse (Figure 3b: with ultrafiltration membrane filter) analyzed by SEC HPLC-ICP-MS. Peaks of high molecular weight and low molecular weight Zn, Cu-binding proteins were observed in the HPLC-ICP-MS chromatogram from the brain supernatant of the 129/ Sv mouse (Figure 3a). The second peak of Zn, Cu-containing proteins eluted at RT=7.6 contained MT-3 and also might contain Cu, Zn- SOD. Using the ultrafiltration membrane filter, high molecular weight metalbinding proteins (MW over 30,000) and especially Cu, Zn-SOD (MW 32,000) were removed from the supernatant in Figure 3b. Thus, the problem of Cu, Zn-SOD and MT-3 overlapping has been solved by using the ultrafiltration membrane filter before applying HPLC-ICPMS. The Zn, Cu-containing proteins were confirmed with authentic samples for MT-1, MT-2 and MT-3. The first peak of Zn, Cu-containing proteins eluted at RT=7.6 in Figure 3b was MT-3. The second peak of the Zn, Cu-containing proteins eluted at RT=8.1, which was a small peak, appeared to be MT-2. The third peak of the Zn, Cu-containing proteins eluted at RT=8.6 was MT-1.

Elution profile of MT-3 in the MT-1, 2 null mouse brain analyzed by HPLC-ICP-MS

Figure 4 shows a chromatogram of the elution profile of the supernatant from the MT-1, -2 null mouse brain after the ultrafiltration membrane filtration analyzed by SEC HPLC-ICP-MS. Because this chromatogram was from the brain supernatant of MT-1, -2 null mice, peaks of MT-1 and MT-2 containing Cu and Zn disappeared. An MT-3 peak containing Cu and Zn was clearly observed in the HPLC-ICPMS chromatogram obtained using 25 mM Tris-12.5 mM HCl buffer containing 20 mM KCl using the ultrafiltration membrane filter. These results revealed that the Cu component of MT-3 compared with Zn in the MT-1, -2 null mouse was larger than that of wild type (129/Sv) mouse (Figure 3b).

Discussion

In this study, we developed a simple separation system for the analysis of MT-1, MT-2 and MT-3 in the brain based on the use of one-step SEC HPLC and on-line coupling with an ICP-MS system. Conventional methods such as metal-saturation assays [20,21], immunochemical methods [22] (radioimmunoassay or ELISAs), and differential pulse polarography have been used by biochemists for the analysis of MTs. However, these techniques suffer from a lack of selectivity to separate different MT isoforms, and are unable to provide information on metal composition. Recently, HPLC followed by metalspecific detection on-line coupling with ICP-MS has been widely used for the detection and determination of metal-binding proteins and MTs in mammalian tissues. Analytical methods of MTs with these hyphenated techniques have been thoroughly reviewed by Prange et al., Ferrarello et al., and Lobinski et al. [9,12,16]. However, in previous studies, no simple system was developed for separating and detecting MT isoforms (MT-1, MT-2, and MT-3) of the brain. HPLC systems with the combination of two different types of chromatography such as SEC and ion-exchange chromatography, or tandem connection with SEC, have often been used [23]. In many studies, it was difficult to separate all of the MT isoforms in the brain completely by one-step chromatography. Peaks of MT-3 and a mixture MT-1 and MT-2 were observed; however, HPLC peaks of MT-1 and MT-2 were eluted with similar RTs and overlapped [13,15,24]. The peaks of MT-3 and Cu, Zn- SOD also might overlap.

SEC (GFC) HPLC is one of the orthodox methods for the separation of metallothioneins that many metallothionein researchers used in the previous studies. We would like to follow the previous research results by using SEC (GFC) HPLC method and to add some modifications to the SEC (GFC) HPLC-ICP-MS method. Therefore, in this study we have tried to develop a simple method by using one-step of SEC HPLC without using anion exchange chromatography after SEC HPLC or reverse-phase HPLC. Certainly reverse-phase HPLC has a benefit to clear separation of many of compounds. However, reverse-phase HPLC needs to use organic solvents like acetonitrile or methanol as mobile phase. If an organic solvent injected into plasma of ICP-MS, due to high carbon content in organic solvents lead to deposition of carbon on the sampling cone. Eventually it leads a reduction in sensitivity, if the ICP-MS instrument is without any incineration system of organic solvents. We would like to develop a simple system with standard ICPMS instrument.

In the system we developed, SEC gel, TSK gel G2000 SW_XL PEEK, a low molecular weight range (5,000-150,000) was chosen to gain clear separation of MT isoforms. TSK gel G2000 SW_XL PEEK does not only involve a size exclusion mechanism, but also may have an ion-exchange mechanism. It was reported that multi-mode gel filtration columns not only have size exclusion but also ion-exchange and reversed phase properties depending on the elution conditions [25]. The TSK gel G2000 SW_XL PEEK used in this study behaved like a multi-mode gel filtration column. We have used the buffer ”25 mM Tris-12.5 mM HCl buffer containing 20 mM KCl” in this study. In our previous studies, HPLCICP- MS results with the buffer 25 mM Tris-12.5 mM HCl without KCl showed non-clear separation of MT-1 and MT-2. After addition of 20 mM KCl to the buffer, we have achieved the clear separation of MT-1 and MT-2. We have considered that the function may due to not only size exclusion mechanism, but also come from the multi-mode gel filtration feature like ion-exchange effects. Table 2 shows advantages and disadvantages of using an ultrafiltration membrane filter before HPLC-ICP-MS analysis of brain MT isoforms. With an ultrafiltration membrane filter, there is an advantages to the removal of high molecular weight proteins and Cu, Zn-SOD.

Table 2: Advantages and disadvantages of using the ultrafiltration membrane filter for HPLC-ICP-MS.

In this study, we had a clear separation of MT-isoforms in the brain using an appropriate buffer (25 mM Tris-12.5 mM HCl containing 20 mM KCl) for the TSK gel G2000 SWXL PEEK column using an ultrafiltration membrane filter. High molecular weight metal-binding proteins and Cu, Zn-SOD were removed from the supernatant using the ultrafiltration membrane filter before injection into the HPLC column. Furthermore, an ultrafiltration membrane filter has the benefit of a gentle preparation instead of precipitation using heating given that heat treatment might alter the MT metal composition. Commercially available columns and equipment are sufficient for analyzing MT isoforms in this system.

It is well known that MT-3 is the dominant isoform of MTs in the brain and we found that MT-1 also was one of the main isoforms of MTs. Although MT-2 accounts for only a small part of the MT isoforms in the brain physiologically, it is detectable using this system. The functional differences of MT-1 and MT-2 have not been well elucidated in the brain, and MT-3 is believed to have a very important role in the central nervous system. The study of MT isoforms with metal component information has great significance. Thus, this analysis system would be a powerful tool for the separation and metal-component analysis of MTs and further research on the biological functions of MT isoforms, especially MT-3 in the brain.

Conclusions

In this study, we developed a simple separation system for analysis of MT-1, MT-2 and MT-3 based on the use of one-step SEC HPLC and on-line coupling with an ICP-MS system. The metal components of the metal-binding proteins eluted by HPLC were continuously detected by ICP-MS. MT-1, MT-2, and MT-3 were clearly separated by this system using an appropriate buffer and membrane filter. This system would be a powerful tool for the separation and metal-component analysis of MTs and further research on the biological functions of MT isoforms in the brain.

Acknowledgments

This work was supported by grants from the Ministry of Education, Culture, Sports, Science, and Technology of Japan. The study was carried out in accordance with the Guide of Animal Experimentation, Tohoku University and the Tohoku University School of Medicine. The authors thank Ms. Chieko Satoh and Ms. Sato Yashima for their excellent technical assistance.

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