Hyphenated techniques for the characterization and quantification of metallothionein isoforms

被引:106
作者
Prange, A [1 ]
Schaumlöffel, D [1 ]
机构
[1] GKSS Forschungszentrum Geesthacht GmbH, Inst Coastal Res Phys & Chem Anal, D-21502 Geesthacht, Germany
关键词
metallothionein isoforms; capillary electrophoresis; high-performance liquid chromatography inductively-coupled plasma-mass;
D O I
10.1007/s00216-002-1350-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Recent developments in the coupling of highly selective separation techniques such as capillary electrophoresis (CE) and high-performance liquid chromatography (HPLC) to element-specific and molecule-specific detectors, such as inductively-coupled plasma mass spectrometry (ICP-MS) and electrospray ionization-tandem mass spectrometry (ESI-MS/MS) for the characterization and quantification of metallothioneins (MTs) are critically reviewed and discussed. This review gives an update based on the literature over the last five years. The coupling of CE to ICP-MS is especially highlighted. As a result of progress in new interface technologies for CE-ICP-MS, research topics presented in the literature are changing from "the characterization of interfaces by metallothioneins" to the "characterization of metallothioneins by CE-ICP-MS". New applications of CE-ICP-MS to the analysis of MTs in real samples are summarized. The potential of the on-line isotope dilution technique for the quantification of MTs and for the determination of the stoichiometric composition of metalloprotein complexes is discussed. Furthermore, a selection of relevant papers dealing with HPLC-ICP-MS for MT analysis are summarized and compared to those dealing with CE-ICP-MS. In particular, the use of size-exclusion (SE)-HPLC as a preliminary separation step for metallothioneins in real samples prior to further chromatographic or electrophoretic separations is considered. Additionally, the application of electrospray ionisation-tandem mass spectrometry (ESI-MS/MS) for the identification of metallothionein isoforms following electrophoretic or chromatographic separation is discussed.
引用
收藏
页码:441 / 453
页数:13
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