Dossier. Metals and Biomolecules. I. Leopold 1, D. Günther 2 and D. Neumann 3. Heavy metal tolerance in plant systems

Similar documents
The Determination of K eq for FeSCN 2+

Synthesis, Isolation, and Purification of an Ester

R E C O M M E N DATION No. 50

P rocess chromatographic purification of pharmaceuticals. Silica-based packing materials for PREP HPLC, SFC and SMB. Dossier

R E C O M M E N DATION No. 43

HEAVY METAL-INDUCED PROTEINS IN CHLAMYDOMONAS REINHARDTII AND THALASSIOSIRA WEISSFLOGII CELLS

A L A BA M A L A W R E V IE W

CADMIUM-PEPTIDES COMPLEXES IN DUNALIELLA SALINA CELLS

R E C O M M E N DATION No. 65

VALVES. V-Series Two-way and Three-way Globe Valve Bodies, Components and Assemblies. F e a t u r e s :

R E C O M M E N DATION No. 51

Liquid storage: Holds the solvent which is going to act as the mobile phase. Pump: Pushes the solvent through to the column at high pressure.

CHROMATOGRAPHY AND MASS SPECTROMETER

United Nations Educat i o n a l, S c i e n t i fic and C u l t u ral Orga n i z at i o n

Keeping Fit. Be t ween 1980 and 2000, t h e. To d ay, i t s more ch a l l e n g i n g. Overview. By Peter Winkler. Science Background.

Chromatography- Separation of mixtures CHEM 212. What is solvent extraction and what is it commonly used for?

HPLC Background Chem 250 F 2008 Page 1 of 24

High Performance Liquid Chromatography

Development and Evaluation of an Albumin-Binding NODAGA-Folate

VALIDATION OF A UPLC METHOD FOR A BENZOCAINE, BUTAMBEN, AND TETRACAINE HYDROCHLORIDE TOPICAL SOLUTION

Chromatographic Separation

Other types of liquid chromatography

Spray Nozzles, Showers, and More

Chromatography & instrumentation in Organic Chemistry

Chromatographic Analysis

ACETONE IN URINE BY UV CODE Z42010

Lec.1 Chemistry Of Water

Introduction to Chromatography

Packings for HPLC. Packings for HPLC

Strategies for the Analysis of Therapeutic Peptides in Biofluids by LC-MS/MS. Lee Goodwin

High Pressure/Performance Liquid Chromatography (HPLC)

CHROMATOGRAPHY, AND MASS SPECTRAL. FRACTIONS OF Lasianthus

Chromatographic Methods: Basics, Advanced HPLC Methods

TR ACE ORGANIC. lgcstandards.com/foodandenvironment

OPTIMIZEFILTRATION. S o lv e n t R e s e r v o i r. I n - l i n e F i l t r a t i o n. I n - L i n e F i l t r a t i o n P r o c e s s

ICP-MS based methods for the quantitative analysis of nanoparticles in biological samples

We help hotels and restaurants SAYHELLO.

GLUTATHIONE IN WHOLE BLOOD BY FLUORIMETRY CODE Z30010

Theory of bulk and flow electrolysis and approach to parameter optimisation for chromatographic electrochemical detection

Lonicera japonica Flower Dry Extract. Proposed For Development Version 0.1. Published on Herbal Medicines Compendium (

Ion Chromatography. Anion Exchange. Chromatography Ion Exchange Theory. Dr. Shulamit Levin

Lonicera japonica Flower Powder. Proposed For Development Version 0.1. Published on Herbal Medicines Compendium (

Open Column Chromatography, GC, TLC, and HPLC

Isotope Dilution Mass Spectrometry

Determination of Hormones in Drinking Water by LC/MS/MS Using an Agilent InfinityLab Poroshell HPH Column (EPA 539)

Chromatography Outline

Cation Exchange HPLC Columns

SUPPLEMENTARY INFORMATION

OVERVIEW INTRODUCTION. Michael O Leary, Jennifer Gough, Tanya Tollifson Waters Corporation, Milford, MA USA

HICHROM. Chromatography Columns and Supplies. LC COLUMNS SIELC Primesep. Catalogue 9. Hichrom Limited

CHEMISTRY Unit 3, Area of Study 1: Chemical Analysis

N e a r- I n f ra red (NIR) spectro s c o py has been grow i n g. NIR calibration in practice. Dossier. Proche Infrarouge PIR

CHEM 3590 Final examination 2017 Instructor : Dr. Hélène Perreault Monday December 11, 1:30-4:30 pm, Frank Kennedy Gold Gym seats

Military High School AL- Ain. Grade 10 &11. Biology Sample Questions. Student Name: Computer #:

T wo-dimensional (2D) corre l ation spectro s c o py has

637. Thiamethoxam. HPLC method

Air Monitoring. Semi-continuous determination of ambient air quality

Beechwood Music Department Staff

Chapter 23 Introduction to Analytical Separations

Application of atmospheric pressure microwave digestion to total Kjeldahl nitrogen determination in pharmaceutical, agricultural and food products

Ion Chromatography (IC)

Section Objectives: Section Objectives: Distinguish mixtures and solutions. Define acids and bases and relate their importance to biological systems.

Chromatography. writing in color

Chemistry Instrumental Analysis Lecture 37. Chem 4631

LC-MS compatible Separation of the Fungicide Spiroxamine

HPLC. High Performance Liquid Chromatography (HPLC) Harris Chapter 25

Advantages of polymerbased. an alternative for ODS

H STO RY OF TH E SA NT

Structure of the α-helix

Packed Column for Ultra-Fast Reversed-Phase Liquid Chromatography, TSKgel Super-ODS. Table of Contents

Rational design of a ratiometric fluorescent probe with a large emission shift for the facile detection of Hg 2+

LC and LC/MS Column Selection Flow Chart

HPLC Winter Webinars Part 2: Sample Preparation for HPLC

User Equilibrium in a Disrupted Network with Real-Time Information and Heterogeneous Risk Attitude

INTRODUCTION. Amino acids occurring in nature have the general structure shown below:

Analytical techniques: Environmental samples. Lecture 2 Universidade do Algarve

Chapter content. Reference

MS-based proteomics to investigate proteins and their modifications

(A) Effect of I-EPI-002, EPI-002 or enzalutamide on dexamethasone (DEX, 10 nm)

1Dissolution Technologies FEBRUARY Refinement of Lower Acceptance Value of the Similarity Factor f 2 incomparison of Dissolution Profiles

P a g e 5 1 of R e p o r t P B 4 / 0 9

HPLC Column Material - Bulk Ware

Chemistry Instrumental Analysis Lecture 28. Chem 4631

LUMEFANTRINUM LUMEFANTRINE

Chromatography. Gas Chromatography

Gas Chromatography (GC)! Environmental Organic Chemistry CEE-PUBH Analysis Topic 5

Technical Note. Introduction

Luminescence transitions. Fluorescence spectroscopy

Ch.28 HPLC. Basic types of Liquid Chromatography Partition (LLC) Adsorption (LSC) Ion Exchange (IC) Size Exclusion (SEC or Gel Chromatography)

Analytical Chemistry

EFFECTS OF MOBILE PHASE COMPOSITION ON THE SEPARATION OF CATECHOLAMINES BY LIQUID CHROMATOGRAPHY WITH ELECTROCHEMICAL DETECTION

Supporting Information

Chemistry in Biology Section 1 Atoms, Elements, and Compounds

Quantitative analysis of small molecules in biological samples. Jeevan Prasain, Ph.D. Department of Pharmacology & Toxicology, UAB.

Chromatography. Chromatography is a combination of two words; * Chromo Meaning color * Graphy representation of something on paper (writing)

High Performance Liquid Chromatography

High Performance Liquid Chromatography

ARTEMETHER AND LUMEFANTRINE ORAL SUSPENSION:Final text for addition to The International Pharmacopoeia (November 2008)

Hole s Human Anatomy and Physiology Eleventh Edition. Chapter 2

Supporting Information. Chemo-enzymatic Synthesis of Isotopically Labeled Nicotinamide Ribose

Transcription:

Application of high performance liquid chromatography - inductively coupled plasma mass spectrometry to the investigation of phytochelatin complexes and their role in heavy metal detoxification in plants I. Leopold 1, D. Günther 2 and D. Neumann 3 1 Laboratory for Materials and Nuclear Processes, Paul Scherrer Institute, 5232 Villigen PSI, Switzerland 2 Institute of Isotope Geology and Mineral Resources, Swiss Institute of Technology Zürich, Sonneggstrasse 5, 8092 Zürich, Switzerland 3 Institute of Plant Biochemistry, Weinberg 3, 06120 Halle, Germany The coupling of size-exclusion chromatography with ICP-MS is shown to be an attractive technique to study the binding of cadmium and copper by phy t o chelatins in plant cell suspension cultures incubated with these metals. Electrospray mass spectrometry enabled to identify the metal binding compounds: (γ-glu-cys) 2 - Gly and (γ-glu-cys) 2. Heavy metal tolerance in plant systems H e avy metals (HMs) like cadmium, c o p p e r, z i n c, l e a d, o r m e rc u ry are env i ronmental pollutants inducing phy s i o l ogi c a l a l t e rations in plants such as growth re t a rd at i o n, m e m b ra n e d a m age, ch a n ges in enzyme activities or induction of ox i d a- t ive stress when their concentrations exceed an element spec i fic thre s h o l d. HM ions interact with SH- and histidy l groups of enzymes and membrane pro t e i n s, leading to inact ivation of the pro t e i n s, cell damage and fi n a l ly cell deat h [1]. Howeve r, a number of plant phenotypes with incre a s e d resistance to HM ions have been isolated from locations that a re polluted with high concentrations of diffe rent metals. The phy s i o l ogical basis of the HM tolerance of these plants can be add ressed either to a reduced uptake of HM ions into the plant cells or to the development of metal-sequesteri n g m e chanisms within diffe rent cellular compartments. Some of these detox i fi c ation mechanisms in HM exposed plants are metal binding to the cell wa l l s, reduced tra n s p o rt across the m e m b ra n e s, a c t ive effl u x, p re c i p i t ation in va c u o l e s, Article available at http://analusis.edpsciences.org or http://dx.doi.org/10.1051/analusis:199826060028 M 28

Dossier synthesis of HM binding compounds such as pep t i d e s, p rot e i n s, o rganic acids or phenolic compounds [2,3]. The storage of HMs inside the vacuoles presumes a t ra n s l o c ation of the HM ions through the cytoplasm. It is w i d e ly accepted that HMs pass the cytoplasm in a ch e l at e d fo rm. For Ni the binding to the imidazole nitrogen of histidine was shown [4]. The synthesis of phy t o ch e l atins (PCs) is a common response of plant cells upon ex p o s u re to HM ions. PCs are small peptides with the ge n e ral stru c t u re (γ G l u C y s ) n G ly (n = 2 11) that are able to ch e l ate HMs due to the high cysteine content in the molecule. The synthesis of PC molecules with diffe rent chain length is induced by a wide va riety of HMs (e. g. A g, B i, C d, C u, H g, P b, S n, Zn [5]), wh e reas the direct part i c i p ation of PCs in the ch e l a- tion of HM ions in plants has been ve ri fied for only few elements under in vivo and in vitro conditions. Ve ry few dat a about the binding pro p e rties of the HM-PC-complexes are k n ow n, m a i n ly due to the pro blem that all the cry s t a l l i s at i o n e ffo rts have failed to dat e. In order to understand the role of these peptides for HM detox i fi c ation in plants and for the d evelopment of HM tolerant phenotypes a detailed know l- e d ge of the metal-binding ch a ra c t e ri s t i c s, s u ch as binding a ffinity or binding stability is needed. Analysis of PC molecules and their HM binding complexes The sep a ration of the dissociated HM-PC-complexes by a reve rsed phase HPLC with post-column derivat i z ation [6] or fl u o rescent labelling of the free SH-groups [7] are comm o n ly used methods for the qualitat ive and quantitat ive a n a lysis of metal-free PC isofo rms. Because the inve s t i gation of the binding pro p e rties and of the HM ions selective ly bound to PC complexes is only possible under non-denat u r- ing conditions, a time consuming combination of diffe re n t ch ro m at ographic pro c e d u res (e. g. gel fi l t ration and ion ch rom at ograp hy) and the subsequent determ i n ation of the HMs by element specific methods (e. g. AAS) in the sep a rat e d f ractions has been mostly ap p l i e d. In a complex biological mat rix trace elements can be present in ionic fo rm, as low or high molecular weight compounds or as organometal complexes. Element specific analytical methods (e. g. A A S, ICP AES or ICP MS) can only d e t e rmine the total content of elements in a sample, but these t e chniques are not able to distinguish between diffe re n t fo rms of an element, the so called s p e c i e s, wh i ch are ve ry i m p o rtant for understanding the biological function or the t oxicity of an element. For the determ i n ation of the concent ration of individual elemental species a sep a ration step of e a ch of these compounds is necessary prior to the analy s i s by A A S, ICP AES or ICP MS. Many of these off-line or online coupled sep a ration and detection systems have been used in the past for speciation analysis in biologi c a l, e nv i- ro n m e n t a l, and clinical re s e a rch. In the present study an on-line coupled high perfo rm a n c e liquid ch ro m at ograp hy - inductive ly coupled plasma mass s p e c t ro m e t ry system (HPLC-ICP MS) was used for the i nve s t i gation of the binding pro p e rties of HM-PC-complexe s in order to ch a ra c t e rise the role of these compounds for the HM detox i fi c ation in HM tolerant and non-tolerant plants. S p e c i ation techniques add ress only a fraction of the total metal content present in the samples, re q u i ring highly sens i t ive analytical detectors. ICP MS was chosen because it has seve ral at t ra c t ive fe at u res compared with other analy t i- cal tech n i q u e s : isotopic info rm ation is ava i l abl e, mu l t i e l e- mental cap ability allows a high sample thro u g h p u t, d e t e c t i o n limits are superior to most conventional techniques with a wide linear dynamic ra n ge of the detector, and most of the elements in the periodic table can be detected. R ega rding the sep a ration technique prior to the element s p e c i fic detection, gas or liquid ch ro m at ograp hy and cap i l- l a ry electro p h o resis are the pre fe rred methods because they a re known as highly efficient for a wide va riety of samples [8]. In pri n c i p l e, e a ch ch ro m at ographic system can be used for species analysis; the selection of the sep a ration method d epends on the sample pro p e rties itself. In comparison to an o ff-line combination of the sep a ration technique and the element specific detector the on-line coupling of both dev i c e s has the gre at adva n t age of a fast time re s o l ved analysis with almost no sample lost or contamination because the sep a- rated compounds are dire c t ly tra n s p o rted to the ex c i t at i o n s o u rce and to the detector and are not collected in fra c t i o n s and stored for subsequent analysis. Due to the fact that the s ep a ration of the components of interest from the sample m at rix is a direct part of the analysis pro c e d u re itself, t i m e consuming sample prep a ration steps such as puri fi c ation and p re c o n c e n t ration can norm a l ly be avo i d e d. A styre n e - d iv i ny l- b e n ze n e - c o p o lymer based size ex clusion ch ro m at ograp h i c column was selected for this study because of low intera c- tions with metals during the sep a ration process compared to silica gels and the possibility of wo rking under isocrat i c conditions with low concentrated bu ffe rs and without any o rganic solvents in the mobile phase, wh i ch is ve ry adva n- t ageous when coupling the HPLC to an ICP MS detector. Sample preparation One of the pro blems of speciation analysis in biologi c a l ex t racts is the development of a rep re s e n t at ive sampling proc e d u re. Unfo rt u n at e ly, i n t e n s ive sample pre t re atment can sign i fi c a n t ly modify the yield of the diffe rent elemental species detected in the sample. In order to ke ep the number of prep a- ration steps as low as possible a ve ry simple ex t raction proc e d u re was used for cell suspension cultures and wh o l e p l a n t s. Water cultures as well as cell suspension cultures of a HM t o l e rant plant, Silene vulga ri s, and of tomato as a non-tolerant plant, i n c u b ated with diffe rent HM ion concentrat i o n s we re used for the analysis of the soluble HM-binding compounds. In order to ch a ra c t e rise the binding affinity and binding stability of HM-PC-complexes the plants we re exposed with essential (Cu 2 +, Z n 2 + ) and non-essential (Cd 2 +, P b 2 + ) HM ions in short- and long-term ex p e riments. The cell suspension cultures we re harvested by suction fi l t rat i o n, washed with 0.1 M EDTA to re m ove ex t ra c e l l u l a ry bound HM ions and immediat e ly fro zen in liquid nitrogen for storage. All sample prep a ration steps for cell cultures and wh o l e plants we re carried out in the same way as described elsewhere [9]. The most important points of the sample pret re atment are a low temperat u re, the addition of 2-merc aptoethanol to all ex t ra c t s, and a ph-value of about 8 in ord e r M 29

to prevent the ox i d ation of the SH-groups in the samples and the dissociation of the HM-binding complexes wh i ch wo u l d occur at ph 6 or lowe r. After the ex t raction pro c e d u re the samples we re dire c t ly analysed without any cl e a nup or conc e n t ration step, minimising the potential risk of contamination. The sep a ration conditions and the detailed operat i n g p a ra m e t e rs of the on-line coupled HPLC-ICP MS system are b ri e fly summarised in table I. Results and discussion All para m e t e rs affecting the resolution of the HPLC sep a rat i o n, s u ch as ph and chemical composition of the mobile p h a s e, and their influence on the ICP mass spectro m e t ri c detection of the transient signals we re inve s t i gated on a PC re fe rence sample well ch a ra c t e rised for the peptide composition. The metal concentration of these sample wa s u n k n own. The best analytical perfo rmance of the HPLC-ICP MS system was ach i eved at a ph value of 7, 10 mm ammonium acetate as the mobile phase and a fl ow rate betwe e n 0.5 and 1.0 ml/min. A lower ph results in the displacement of the HM ions from the PC-complex; a higher concentration of the ammonium acetate leads to an increase of the b a ck ground intensity for diffe rent elements (e. g. Zn) and t h e re fo re to a deteri o ration of the detection limits. The analysis of ex t racts of Silene vulga ri s and tomato cell suspension cultures shows a new ly synthesised compound with a molecular weight of ap p rox i m at e ly 13000 Da wh i ch can be observed in the UV ch ro m at ogram and was not d e t e c t able in the control plants (Fi g. 1). The corre s p o n d i n g t ransient ICP MS signals of these ex t racts cl e a rly indicat e t h at this compound is a HM-binding complex with the applied HM ions in both cell suspension cultures (Fi g. 2). I n fo rm ations about the stru c t u re of the HM-binding complex a re not ava i l able from the HPLC-ICP MS measure m e n t s. Th e re fo re, the puri fied HM-binding compound of both cell Figure 1. HPLC chromatograms of soluble extracts from tomato cell suspension cultures 5 h after HM incubation. a) contro l cells, b) cell cultures incubated with 1 mm Cd 2+. The peak indicated by an arrow corresponds to the HM-induced compound with an estimated molecular weight of approximately 13000 Da. Elution with 0.5 ml/min 10 mm ammonium acetate, ph 7. For Silene vulgaris cell suspension cultures see [7]. Table I. Chromatographic conditions and operating parameters of the HPLC-ICP MS system. H P L C Mobile phase 10 mm ammonium acetate, ph 7 F l ow ra t e 0.5 1.0 ml/min Death time betwe e n 30 60 s UV and ICP-MS d e t e c t o r I n j e c tion vo l u m e 20 µl I C P - M S RF fo r ward powe r 1350 W Reflected powe r < 5 W Cool gas flow 13 L/min Au x i l i a ry gas flow 0.8 L/min N e bu l i zer gas flow 0.74 L/min Data aquisition mode Peak jumping Points per peak 1 D well time 20.48 ms suspension cultures we re analysed by electro s p ray ionisat i o n mass spectro m e t ry (ESI MS). Fi g u re 3 shows the ESI mass s p e c t rum of the HM-binding complex from a tomato cell suspension culture incubated with 0.01 mm Cu 2 + and Cd 2 +. For tomato as well as for Silene vulga ri s ( d ata not show n ) the HM-binding complexes can be cl e a rly identified from the ICP MS measurements and the ESI mass spectra as a comp l ex of HM ions and PC or desgly-pc molecules with the s t ru c t u re (γ G l u C y s ) 2 G ly and (γ G l u C y s ) 2. PC molecules with n > 2 are not found in the HM-PC-complexe s after 24 h of HM exposition. The S-S-bonds observed in the mass spectrum seems to result from re a rra n gement re a c t i o n s d u ring the ionisation process or from the dissociation of the H M - P C - c o m p l exes. It is not cl e a r, whether the desgly - P C - molecules are constituents of the HM-PC-complex with a function in HM-binding or if they are produced during the i o n i s ation pro c e s s. In roots and leaves of water cultures of Silene vulga ri s and tomato and in cell cultures exposed to equivalent conc e n t rations of Cu 2 +, C d 2 +, P b 2 + and Zn 2 + o n ly Cu- and Cd- P C - c o m p l exes are detectable in the ex t ra c t s, while Pb and Zn are bound to non-ch a ra c t e rised lower molecular we i g h t c o m p o u n d s. In vivo a n d in vitro s at u ration ex p e riments with M 30

Dossier Figure 2. ICP-MS signals of the isotope 114 Cd in the soluble extracts of a tomato cell suspension culture incubated with 1 mm Cd 2+ for up to 5 hours. The peak with a retention time of approximately 17.5 min corresponds to the new synthesised compound indicated by an arrow in figure 1. Elution with 0.5 ml/min 10 mm ammonium acetate, ph 7. The time difference between the UV and the ICP-MS detector was ca. 60 s. Figure 3. ESI mass spectrum of the purified HM-binding compound from a tomato cell suspension culture incubated with 0.01 mm Cu 2 + and Cd 2 + for 24 h. P C 2 corresponds to (γ Glu Cys) 2 Gly; desgly PC 2 to (γ Glu Cys) 2. d i ffe rent concentrated Cu 2 + - and Cd 2 + -solutions confi rm e d the higher binding stability of Cu 2 + ions in the PC-complexe s in comparison to Cd 2 + [ 9 ]. The amounts of HM ions in the soluble fractions of the samples we re quantified from the HPLC-ICP MS ex p e riments using HM-EDTA-solutions injected dow n - s t ream fro m the sep a ration column as calibration standards. Cert i fied re f- e rence mat e rials for the speciation of low and high molecular weight HM-binding components in biological samples a re not ava i l abl e. Th e re fo re, a metallothionein-standard fro m rabbit liver (Sigma, St Louis, USA) was analysed to estimat e the accura cy of the quantitat ive pro c e d u re. The re c ove ry wa s d e t e rmined to be better than 90% (n = 5), despite memory e ffects on the column mat e rial. The total HM concentrat i o n s in the cell suspension cultures and whole plants we re determined by direct nebu l i z ation into the ICP MS after m i c rowave digestion. The comparison of the results of both q u a n t i t at ive measurements shows that only a minor part of the total HM concentration is present in a soluble fo rm as well in cell suspension cultures (less then 5%) as in wh o l e plants (less then 25%). The inve s t i gation of HM tolerant Silene cucubalus, M i nu a rtia ve rn a, a n d A rm e ria maritima plants grown on a m e d i eval copper mining region ( Saugru n d, E i s l eb e n, G e rm a ny) shows no fo rm ation of HM-PC-complexes in these plants. The HM ions in the soluble ex t racts are ex cl u- s ive ly bound to lower molecular weight compounds. Th e s e results explain that PCs are not the major source of the high HM tolerance of these plants, although these plants are abl e to synthesise HM-PC-complexes as could be revealed in the water cultures. Using electron microscopic inve s t i gat i o n s combined with element-specific techniques it was confi rm e d t h at a couple of other mechanisms (e. g. HM ex c retion by s p e c i fic glands or hy d athodes in the leave s, binding of HM ions on proteins or silicates in an insoluble fo rm, s t o rage of HM ions in the intercellular spaces of the leaf pare n chy m a ) is invo l ved in the detox i fi c ation of high concentrations of essential and non-essential elements in the HM-tolera n t plants of the copper mining region [3,10]. Conclusion The ap p l i c ation of diffe rent concentrated HM solutions to cell suspension cultures and water cultures induces the synthesis of HM-PC-complexes with Cu and Cd ions as well in the HM tolerant Silene vulga ri s as in the non-tolerant tomat o under ex p e rimental conditions. Zn and Pb ions are ex cl u- s ive ly bound to lower molecular weight substances in all i nve s t i gated plant systems. HM-PC-complexes we re not M 31

synthesised in HM tolerant Silene cucubalus plants grow n on a medieval copper mining dump showing that PCs are not mainly re s p o n s i ble for the HM tolerance of these special phenotypes under nat u ral conditions. The high sensitivity of ICP MS combined with its ab i l i t y to deal with a liquid eluent at typical ch ro m at ographic fl ow rates makes it an useful detector for multielemental speciation analysis in combination with a sep a ration tech n i q u e. A n on-line coupled HPLC-ICP MS system was successfully used for the ch a ra c t e ri s ation of HM-PC-complexes of diffe rent plant systems and for the inve s t i gation of the binding p ro p e rties of these components under in vivo and in vitro conditions. Howeve r, t h e re are a couple of limitations of this a n a lytical system re s t ricting the ap p l i c ability of the technique especially for many biological samples. Low concent rations of sulphur or nitrogen wh i ch would be important fo r the qualitat ive or even quantitat ive analysis of amino acids or proteins as binding part n e rs of trace elements are not d e t e c t able with ICP MS due to the high back ground signal on these elements. Furt h e rm o re, the determ i n ation of uncomp l exed metal ions in the sample is hard ly possible because t h ey can be adsorbed to some extent on the size ex cl u s i o n column mat e rial. Because cert i fied re fe rence mat e rials fo r these types of HM-complexes are not ava i l able until now, the ve ri fi c ation of quantitat ive results is complicat e d. Eve n c o n s i d e ring the limitations of this system, the re s u l t s obtained in the present study show the gre at potential of ch ro m at ographic techniques combined with an elemental detector. The careful optimisation of all parameters influencing the HPLC-ICP MS system and a accurate sample p rep a ration lead to analytical results wh i ch allow more detailed insides into particular biological pro c e s s e s. Acknowledgements We thank Dr. Jürgen Schmidt from the Institute of Plant B i o ch e m i s t ry for the ESI-MS analy s e s. References 1. Va l l e, B. L.; Ulmer, D. D. Ann. Rev. Bioch e m. 1 9 7 2, 4 1, 9 1. 2. E rn s t, W. H. O.; Ve rk l e i j, J. A. C.; Sch at, H. Acta Bot. Neerl. 1 9 9 2, 4 1, 2 2 9. 3. N e u m a n n, D.; zur Nieden, U.; Lich t e n b e rge r, O.; Leopold, I. J. Plant. Phy s i o l. 1 9 9 5, 1 4 6, 7 0 4. 4. K r ä m e r, U.; Cotter- H owe l l s, J. D.; Charn o ck, J. M.; Bake r, A. J. M.; Smith, J. A. C. N at u re 1 9 9 6, 3 7 9, 6 3 5. 5. Z e n k, M. H. G e n e 1 9 9 6, 1 7 9, 2 1. 6. G ri l l, E.; Wi n n a cke r, E. L.; Zenk, M. H. Meth. Enzymol. 1 9 9 1, 2 0 5, 3 3 3. 7. R i j s t e n b i l, J. W.; Wi j n h o l d s, J. A. M a rine Biol. 1 9 9 6, 1 2 7, 4 5. 8. Ve l a, N. P.; Caru s o, J. A. J. Anal. At. Spectro m. 1 9 9 3, 8, 7 8 7. 9. L e o p o l d, I.; Günther, D. Fresenius J. Anal. Chem. 1 9 9 7, 3 5 9, 3 6 4. 1 0. N e u m a n n, D. zur Nieden, U.; Sch w i ege r, W.; Leopold, I. ; L i ch t e n b e rge r, O. J. Plant. Phy s i o l. 1 9 9 7, 1 5 1, 1 0 1. M 32