Productivity in large areas of the world's oceans is limited by low concentrations of dissolved iron in surface waters. Phytoplankton have adapted to persist in these environments by reducing their requirements for iron (Fe) in key metabolic pathways, in some cases by replacing Fe-containing catalysts with their iron-free functional equivalents. This thesis examines the requirements and biochemical roles for copper (Cu) and manganese (Mn) in Fe-limited centric marine diatoms. A major finding of my research is that diatoms have elevated requirements for Mn and Cu when grown in Fe-deficient seawater. Iron deficiency induces oxidative stress and increases the cellular concentrations of toxic oxygen radicals and damage products in Thalassiosira pseudonana. The increased Mn-requirement is used, in part, to activate Mn-containing isoforms of the antioxidant enzyme superoxide dismutase. Cultures co-limited by Fe and Mn exhibit high levels of oxidative stress and an inefficient detoxification pathway that further reduces cell growth. Diatoms isolated from the metal poor open ocean require more Cu to divide than related species from metal-rich coastal waters. This pattern is in stark contrast to all other known nutritive trace metals. One part of the diatom Cu requirement that is independent of provenance is for efficient Fe transport. The additional Cu requirement of oceanic species appears to be due to the constitutive expression of a Cu-containing electron transport protein, possibly plastocyanin. Coastal species, which have higher Fe-requirements for growth, retain the Fe-containing functional homologue cytochrome c6. By employing metals other than Fe within photosynthesis and antioxidant pathways, marine diatoms are able to increase their fitness in Fe-deficient environments. However, Mn and Cu also occur in low concentrations in the open ocean and thus may co-limit growth of natural populations of phytoplankton. Metal enrichment experiments i

Changes in copper metabolism have been reported in both thermal injury and skeletal trauma; data regarding copper status in multiple trauma patients (MTP) are nonexistent. Hypercatabolism following multiple trauma may increase copper utilization, deplete copper stores and compromise cuproenzyme synthesis and function. The purpose of this study was to provide information on copper status in MTP and determine whether age, injury severity, clinical outcome or nutritional intake influenced copper status. Twenty-four hour copper losses, serum copper and ceruloplasmin were measured in 11 MTP with Injury Severity Scores (ISS) >12 at 24-48 hours post admission. Collections of biological fluids (urine, nasogastric, chest tube, drains, stools) were analyzed for copper using atomic absorption spectrophotometry (AAS) and quantified over 5 days. Serial serum copper and ceruloplasmin were determined on days 1,3,5,10,15 and patient discharge by ASS and rate nephelometry inmunoprecipition, respectively. Eight patients received parenteral nutrition (PN). Three received intravenous glucose/electrolyte infusions (IV). urine (n=11) and nasogastric losses (n=8) were statistically greater than normal (p<.001). The mean ± SEM cumulative copper losses of urine, chest tube drainage, nasogastric secretions and other drains were 790 ± 116 (n=11), 833 ± 130 (n=7), 261 ± 46 (n+8), and 150 ± 58 μg/5 d (n=8), respectively. Urinary losses represented 10 to 12 times the normal copper excretion. Serum copper on day 1 and ceruloplasmin day 3 were significantly higher than normal (p<.025). Cumulative copper balance in the IV group was - 2266 μg and -440 μg in the PN group. No relationship was found between copper loss and ISS. Patients in their twenties demonstrated the greatest urinary copper loss. The physiological and biochemical effects of extensive copper loss in the MTP require further evaluation. These patients may have a predisposition to copper deficiency due to excessive copper losses and may require increased copper supplementation. / Ph. D.

The object of this study is to determine the copper and iron intake in food and the output in the urine and feces of women students living in the Home Management House eating a self-selected diet.

The effects of sublethal copper on metabolism were in vestigated in bluegill (Lepomis macrochirus) by measuring whole body oxygen consumption in fish exposed to sublethal copper alone and in conjunction with a temperature increase. In vitro oxygen consumptions of liver, brain, and gill were also measured under these two conditions, as was the accumulation of copper in these tissues. In addition, the concentration of copper in bile was measured. Copper was found to decrease whole body oxygen consumption in animals exposed to copper alone, although the oxygen consumptions of tissues were not significantly altered. This indicates that copper is acting to decrease VO₂ at a higher level of integration than the individual tissues. In animals subjected to an increase in temperature as well as sublethal copper, oxygen consumption was higher than controls five days after the temperature was increased, indicating a delay in temperature acclimation. This increase was reflected in higher in vitro oxygen consumption in the liver and gill indicating that sublethal copper delays temperature acclimation by acting directly on the tissues. Tissue copper accumulation was seen first in the gills followed by accumulation in the liver. Copper was not found to accumulate in the brain. Increased copper levels were found in the bile at all tested exposure times. A discussion of the ecological implications of these findings is included. / M. S.

Le cuivre (Cu) est un nutriment essentiel à la vie des organismes mais aussi, lorsqu’il est présent en excès, un constituant toxique de la cellule. Pour faire face à des concentrations élevées en Cu dans l’environnement, les plantes ont développé des mécanismes complexes d’homéostasie et de tolérance au Cu. L’objectif de ce travail est d’apporter une contribution à la compréhension de ces mécanismes en utilisant la plante modèle Arabidopsis thaliana. Dans un premier temps, nous avons montré que l’excès de Cu2+ entraînait une réorganisation de l’architecture du système racinaire caractérisée par une inhibition de la croissance de la racine primaire et l’augmentation de la densité de racines latérales. Nous avons mis en évidence plusieurs processus métaboliques qui pourraient être impliqués dans cette réorganisation, tels que des changements dans l’homéostasie minérale, le statut hormonal, et la production de lignine. Une approche de génétique classique a ensuite été entreprise afin de mieux comprendre les composants moléculaires impliqués dans cette réponse. Un criblage de mutants a été effectué sur excès de Cu2+ dans le but d’isoler des mutants présentant un phénotype racinaire altéré par le Cu2+. Un mutant sensible au Cu2+ (appelé cop29) a été sélectionné en raison de sa forte inhibition de croissance racinaire sur excès de Cu2+. Le clonage positionnel du mutant, combiné avec des approches génomiques, a permis d’identifier le gène At3g14190 comme étant le gène muté responsable du phénotype de cop29. Ce gène encode une protéine de fonction encore inconnue. La caractérisation phénotypique de cop29 a révélé que le mutant était également sensible à l’excès de Zn2+, Mn2+ et Na+. De plus, nous avons montré qu’en présence d’un excès de Cu2+ ou de NaCl le mutant présentait des concentrations en K+ significativement plus faibles que le type sauvage. Etant donné que le maintien de l’homéostasie du K+ joue un rôle essentiel dans la tolérance des plantes à l’excès de Cu ou de NaCl, nous avons émis l’hypothèse que ces faibles concentrations en K+ pourraient être la cause du phénotype de cop29. Par ailleurs, l’utilisation des banques de données génomiques et protéomiques a mis en avant que la protéine COP29 pourrait également jouer un rôle dans la régulation du cycle cellulaire. Les perspectives consisteront à découvrir la fonction de la protéine COP29 et contribueront ainsi à mettre en évidence un nouveau composant moléculaire impliqué dans la tolérance des plantes aux stress. / Doctorat en Sciences / info:eu-repo/semantics/nonPublished

[ES] La enfermedad de Wilson (EW) es un trastorno hereditario del metabolismo del cobre causado por mutaciones en ATP7B, que codifica una proteína transportadora de cobre en el hígado. Su mal funcionamiento provoca un fallo en la excreción biliar de cobre y una acumulación progresiva de este metal en el organismo, especialmente en hígado y cerebro. En este trabajo, se explora la posible utilidad de miRNAs circulantes en plasma para identificar biomarcadores que sirvan para controlar la progresión de la enfermedad en pacientes con EW bajo tratamiento. Los modelos desarrollados para cada miRNA mostraron un buen rendimiento al clasificar a los pacientes con factores de evolución desfavorable, por lo que estos tres miRNAs se proponen como candidatos para mejorar el seguimiento clínico o para respaldar la eficacia de nuevas terapias en la EW. / [CA] La malaltia de Wilson és un trastorn hereditari del metabolisme del coure causat per mutacions en ATP7B, que codifica per a una proteïna transportadora del coure al fetge. El seu mal funcionament produeix alteracions en l'excreció biliar i l'acumulació progressiva de coure, especialment en fetge i cervell. Es va explorar la possible utilitat del perfil de miRNAs circulants com biomarcadors de progressió de la patologia hepàtica. L'avaluació dels models obtinguts per a cadascun dels tres miRNAs va mostrar un bon rendiment per a classificar al grup de pacients amb factors d’evolució desfavorable, en conseqüència, es proposen com a candidats per tal de millorar el seguiment clínic o comprovar l’efectivitat de noves teràpies en la malaltia de Wilson. / [EN] Wilson disease (WD) is an inherited disorder of copper metabolism caused by mutations in ATP7B, which encodes for a liver copper-transporting protein. Its dysfunction causes a deficit in biliary copper excretion and a progressive accumulation of this metal in the organism, mainly in liver and brain. In this work, circulating miRNAs profiling in plasma has been accomplished to identify biomarkers that could serve to monitor disease progression in WD patients under chelation therapy. Developed models for each miRNA exhibited good performance classifying patients with poor outcome factors, consequently, these three miRNAs are proposed as candidates to improve clinical follow-up or to support efficacy of novel therapies in WD. / Esta Tesis Doctoral ha sido financiada por los siguientes proyectos de investigación: “Avanzar en el diagnóstico y la prognosis de la enfermedad de Wilson” Duración: 2016-2019, Fundació Per Amor a l’Art (FPAA) IP: C. Espinós; “Bases genéticas y biomarcadores pronóstico de la enfermedad de Wilson y Wilson-like” 2020-2022, Fundació Per Amor a l’Art (FPAA) IP: C. Espinós; “Estudios clínicos, bases genéticas y biomarcadores pronóstico en enfermedades raras neurodegenerativas” 2019-2021, Instituto de Salud Carlos III (Expediente: PI18/00147) IP: C. Espinós; “De genes a terapia en enfermedades neurodegenerativas y neuromusculares” 2018-2021, Generalitat Valenciana, Programa Prometeo para grupos de investigación de excelencia (Expediente: PROMETEO/2018/135) Consorcio de investigadores formado por F. V. Pallardó (coordinador), J.M. Millán, I. Galindo, P. Sanz, T. Sevilla y C. Espinós. / Sánchez Monteagudo, A. (2021). Genética molecular y biomarcadores de la enfermedad de Wilson [Tesis doctoral]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/171454

Neste trabalho, alguns novos complexos imínicos de cobre(II) com ligantes inspirados em biomoléculas como oxindóis, contendo grupos indólicos, imidazólicos ou pirrólicos com diferentes características estruturais, foram sintetizados e caracterizados por análise elementar, espectrometria ESI-MS e espectroscopias IV, UVNis e EPR. As possíveis interações desses complexos de cobre com a albumina humana (HSA) e com o plasma sanguíneo foram estudadas através das técnicas EPR, CD e SDS-PAGE, indicando que estas ocorrem principalmente no sítio N-terminal da proteína. Suas reatividades frente a compostos biológicos relevantes, tais como glutationa, ascorbato e peróxido de hidrogênio, também foram verificadas. Alguns dos complexos estudados podem ser ativados por glutationa, ascorbato ou peróxido de hidrogênio, sendo capazes de gerar espécies reativas de oxigênio em concentrações significativas, na presença desses redutores ou oxidantes biológicos. Adicionalmente, as propriedades pró-oxidantes de tais complexos foram investigadas, visando elucidar estudos prévios de suas atividades pró-apoptótica e antitumoral. Alguns destes complexos foram mais eficientes em causar danos oxidativos à 2-deoxi-D-ribose, enquanto outros foram mais eficientes em causar oxidantes na proteína HSA, com formação de grupos carbonílicos, principalmente em presença de H202. Experimentos de CD complementaram estes resultados, indicando que somente alguns complexos causaram modificações na &#945;-hélice da proteína. Experimentos de EPR com captador de spin, na presença de HSA e H202, mostraram a formação de quantidades apreciáveis de radicais hidroxil e radicais de carbono, em presença de peróxido de hidrogênio. Além disso, os complexos apresentaram notável habilidade de ligação ao DNA e conseqüente atividade nuclease, promovendo clivagens nas duas fitas. Experimentos de fluorescência, EPR, gel de eletroforese marcado com &#945;-32P-UTP e CD foram ainda realizados, visando elucidar o mecanismo de ação destes complexos no meio biológico. Estes experimentos indicaram que eles podem se associar ao DNA, através de suas bases ou pela interação com a deoxi-ribose, já que promoveram danos oxidativos nestes substratos. Entretanto, não catalisam a hidrólise dos grupos fosfato, atuando, portanto, predominantemente por um mecanismo oxidativo. Através de CD, poucas perturbações na elipsicidade do DNA foram observadas, o que indica que estes complexos provavelmente estão localizadas nas cavidades ou alças do ácido nucléico. / Some novel imine-copper(II) complexes with ligands inspired in biomolecules such as oxindoles, containing indole, pirrole or imidazole moieties with different structural features were synthesized, and characterized by elemental analysis, IV, UV/Vis and EPR spectroscopies, and ESI-MS spectrommetry. Interactions of these complexes with human serum albumin (HSA) and human plasma were verified by EPR, CD and SDS-PAGE techniques, showing that they occur mainly at the N-terminal site of the protein. Their reactivity towards biological relevant compounds, such as glutathione, ascorbate and hydrogen peroxide were also verified; some of them are capable of generating ROS in significant concentrations, in the presence of these reducing or oxidant agents. Additionally, the activity of such copper(II) complexes in promoting oxidative damage to different substrates was investigated, in order to elucidate previous studies on their pro-apoptotic and antitumoral activity. Some of these complexes were much more efficient to cause oxidative damage to 2-deoxy-D-ribose, especially in the presence of hydrogen peroxide. On the contrary, others were more active in causing damage to HSA protein, with the formation of carbonyl groups. Experiments by CD corroborated these results, since only some of the complexes caused modifications in the protein -helix. EPR spin trapping experiments, in the presence of HSA and H2O2, showed significant generation of hydroxyl as well as carbon centered radicals. Moreover, all the complexes showed remarkable ability to bind to DNA, promoting double-strand cleavage, upon H2O2 activation. In order to investigate their mechanism of action, fluorescence, EPR, gel-electrophoresis with labeled &#945;-32P-UTP and CD experiments were carried out. The results indicated that these complexes can bind to DNA through its bases or can interact with the deoxi-ribose rings, promoting oxidative damage to those substrates. On the contrary, they do not catalyze the hydrolysis of phosphate groups. By CD spectroscopy, little perturbations on the helicity conformation of the DNA were observed, indicating that these complexes are probably located in the grooves.

Neste trabalho, alguns novos complexos imínicos de cobre(II) com ligantes inspirados em biomoléculas como oxindóis, contendo grupos indólicos, imidazólicos ou pirrólicos com diferentes características estruturais, foram sintetizados e caracterizados por análise elementar, espectrometria ESI-MS e espectroscopias IV, UVNis e EPR. As possíveis interações desses complexos de cobre com a albumina humana (HSA) e com o plasma sanguíneo foram estudadas através das técnicas EPR, CD e SDS-PAGE, indicando que estas ocorrem principalmente no sítio N-terminal da proteína. Suas reatividades frente a compostos biológicos relevantes, tais como glutationa, ascorbato e peróxido de hidrogênio, também foram verificadas. Alguns dos complexos estudados podem ser ativados por glutationa, ascorbato ou peróxido de hidrogênio, sendo capazes de gerar espécies reativas de oxigênio em concentrações significativas, na presença desses redutores ou oxidantes biológicos. Adicionalmente, as propriedades pró-oxidantes de tais complexos foram investigadas, visando elucidar estudos prévios de suas atividades pró-apoptótica e antitumoral. Alguns destes complexos foram mais eficientes em causar danos oxidativos à 2-deoxi-D-ribose, enquanto outros foram mais eficientes em causar oxidantes na proteína HSA, com formação de grupos carbonílicos, principalmente em presença de H202. Experimentos de CD complementaram estes resultados, indicando que somente alguns complexos causaram modificações na &#945;-hélice da proteína. Experimentos de EPR com captador de spin, na presença de HSA e H202, mostraram a formação de quantidades apreciáveis de radicais hidroxil e radicais de carbono, em presença de peróxido de hidrogênio. Além disso, os complexos apresentaram notável habilidade de ligação ao DNA e conseqüente atividade nuclease, promovendo clivagens nas duas fitas. Experimentos de fluorescência, EPR, gel de eletroforese marcado com &#945;-32P-UTP e CD foram ainda realizados, visando elucidar o mecanismo de ação destes complexos no meio biológico. Estes experimentos indicaram que eles podem se associar ao DNA, através de suas bases ou pela interação com a deoxi-ribose, já que promoveram danos oxidativos nestes substratos. Entretanto, não catalisam a hidrólise dos grupos fosfato, atuando, portanto, predominantemente por um mecanismo oxidativo. Através de CD, poucas perturbações na elipsicidade do DNA foram observadas, o que indica que estes complexos provavelmente estão localizadas nas cavidades ou alças do ácido nucléico. / Some novel imine-copper(II) complexes with ligands inspired in biomolecules such as oxindoles, containing indole, pirrole or imidazole moieties with different structural features were synthesized, and characterized by elemental analysis, IV, UV/Vis and EPR spectroscopies, and ESI-MS spectrommetry. Interactions of these complexes with human serum albumin (HSA) and human plasma were verified by EPR, CD and SDS-PAGE techniques, showing that they occur mainly at the N-terminal site of the protein. Their reactivity towards biological relevant compounds, such as glutathione, ascorbate and hydrogen peroxide were also verified; some of them are capable of generating ROS in significant concentrations, in the presence of these reducing or oxidant agents. Additionally, the activity of such copper(II) complexes in promoting oxidative damage to different substrates was investigated, in order to elucidate previous studies on their pro-apoptotic and antitumoral activity. Some of these complexes were much more efficient to cause oxidative damage to 2-deoxy-D-ribose, especially in the presence of hydrogen peroxide. On the contrary, others were more active in causing damage to HSA protein, with the formation of carbonyl groups. Experiments by CD corroborated these results, since only some of the complexes caused modifications in the protein -helix. EPR spin trapping experiments, in the presence of HSA and H2O2, showed significant generation of hydroxyl as well as carbon centered radicals. Moreover, all the complexes showed remarkable ability to bind to DNA, promoting double-strand cleavage, upon H2O2 activation. In order to investigate their mechanism of action, fluorescence, EPR, gel-electrophoresis with labeled &#945;-32P-UTP and CD experiments were carried out. The results indicated that these complexes can bind to DNA through its bases or can interact with the deoxi-ribose rings, promoting oxidative damage to those substrates. On the contrary, they do not catalyze the hydrolysis of phosphate groups. By CD spectroscopy, little perturbations on the helicity conformation of the DNA were observed, indicating that these complexes are probably located in the grooves.

Szeto Tsz Kwan Leo. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2005. / Includes bibliographical references (leaves 112-120). / Abstracts in English and Chinese. / Abstract --- p.i / 摘要 --- p.iii / Acknowledgements --- p.v / Table of Contents --- p.vi / List of Tables --- p.ix / List of Figures --- p.x / Abbreviations --- p.xii / Chapter Chapter 1 --- Introduction --- p.1 / Chapter 1.1 --- Heavy metals contaminations in Shing Mun River --- p.1 / Chapter 1.1 --- Importance of copper regulation and role of liverin copper metabolism --- p.6 / Chapter 1.1.1 --- Role of copper --- p.6 / Chapter 1.1.2 --- Toxicity due to unbalanced copper regulation --- p.7 / Chapter 1.1.3 --- Function of liver in copper detoxification --- p.9 / Chapter 1.2 --- Aims and rationale of this research --- p.11 / Chapter Chapter 2 --- Heavy metal concentrations of tilapia samples collected from Shing Mun River --- p.12 / Chapter 2.1 --- Introduction --- p.12 / Chapter 2.1.1 --- Sampling sites - Fo Tan and Siu Lek Yuen Nullah --- p.12 / Chapter 2.1.2 --- Tilapia samples collected from the sites --- p.16 / Chapter 2.1.3 --- Tilapia as a study model --- p.18 / Chapter 2.1.4 --- Bioavailability of heavy metals in water --- p.19 / Chapter 2.1.5 --- Metal content in liver --- p.20 / Chapter 2.1.6 --- Aim of this chapter --- p.20 / Chapter 2.2 --- Materials and Methods --- p.22 / Chapter 2.2.1 --- Collection of control and field samples --- p.22 / Chapter 2.2.2 --- Heavy metal concentrations determination --- p.23 / Chapter 2.2.3 --- Homogenization of liver cells --- p.24 / Chapter 2.2.4 --- Subcellular fractionation --- p.24 / Chapter 2.2.5 --- Determination of copper and zinc content in each subcellular fraction --- p.253 / Chapter 2.3 --- Results --- p.27 / Chapter 2.3.1 --- Physical data --- p.27 / Chapter 2.3.2 --- Metal concentrations in liver and muscle --- p.27 / Chapter 2.3.3 --- Copper and zinc subcellular distribution in liver cell --- p.33 / Chapter 2.4 --- Discussion --- p.36 / Chapter 2.4.1 --- Difference in metal concentration between sites --- p.36 / Chapter 2.4.2 --- Copper contamination in water and fish organ (muscle and liver) from the Shing Mun River --- p.36 / Chapter 2.4.3 --- Comparison of metal content in muscle and liver at Fo Tan site with previous studies --- p.39 / Chapter 2.4.4 --- Copper and zinc concentrations in the liver of tilapia --- p.42 / Chapter 2.4.5 --- Copper and zinc sebcellular distribution in the liver of tilapia --- p.43 / Chapter Chapter 3 --- Column chromatography of hepatic proteins from tilapias --- p.44 / Chapter 3.1 --- Transport of metals from circulatory system to liver --- p.44 / Chapter 3.1.1 --- Copper transporting plasma proteins in vertebrates --- p.44 / Chapter 3.1.2 --- Copper uptake into hepatocytes --- p.45 / Chapter 3.1.3 --- Intracellular metabolism of copper --- p.48 / Chapter 3.1.4 --- Mechanism of copper toxicity following excess accumulation --- p.49 / Chapter 3.1.5 --- Aim of this chapter --- p.50 / Chapter 3.2 --- Materials and Methods --- p.51 / Chapter 3.2.1 --- Purification of liver cytosolic proteins by gel-filtration column chromatography --- p.51 / Chapter 3.2.2 --- Copper content detection in elution --- p.52 / Chapter 3.2.3 --- Analysis of peaks from elution profile using tricine gel SDS PAGE --- p.53 / Chapter 3.3 --- Results --- p.55 / Chapter 3.3.1 --- Gel-filtration liquid chromatography elution profiles --- p.55 / Chapter 3.3.2 --- SDS PAGE analysis of peaks in elution profiles --- p.51 / Chapter 3.4 --- Discussion --- p.54 / Chapter 3.4.1 --- Comparison of gel filtration profiles of sample liver cytosol between sites and sexes --- p.64 / Chapter 3.4.2 --- Possible proteins in peaks found in the gel filtration profiles --- p.64 / Chapter 3.4.3 --- Common copper-indeced proteins --- p.67 / Chapter 3.5 --- Conclusion --- p.70 / Chapter Chapter 4 --- Two-dimensional electrophoresis of hepatic cutosol of tilapias caught from Shing Mun River and copper-treated HEPA T1 cell --- p.72 / Chapter 4.1 --- Introduction --- p.72 / Chapter 4.1.1 --- The need of ´بin vitro' experiment --- p.72 / Chapter 4.1.2 --- Choice of cell line --- p.73 / Chapter 4.1.3 --- Aim of this chapter --- p.74 / Chapter 4.2 --- Materials and Methods --- p.76 / Chapter 4.2.1 --- HEPA T1 cell cultivation --- p.76 / Chapter 4.2.2 --- Copper exposure of HEPA T1 cell --- p.77 / Chapter 4.2.3 --- Subcellular protein extraction of the copper-treated HEPA T1 cells --- p.77 / Chapter 4.2.4 --- Bicinchoninic Acidic (BCA) Protein Assay --- p.79 / Chapter 4.2.5 --- Two-dimensional gel electrophoresis --- p.79 / Chapter 4.3 --- Results --- p.83 / Chapter 4.3.1 --- Graphical presentation of spots observed on 2-dimensional gel of field samples and copper-injected samples --- p.33 / Chapter 4.3.2 --- Graphical presentation of spots detected on 2-dimensional gel of HEPAT1 cells --- p.84 / Chapter 4.3.3 --- Comparison of matched spots on 2-dimensional gels among control and copper-treated HEPAT1 cells --- p.97 / Chapter 4.4 --- Discussion --- p.105 / Chapter 4.4.1 --- Comparison of the spot patterns between field sample and copperOtreated HEPA T1 cells --- p.105 / Chapter 4.5 --- Conclusion --- p.107 / Chapter Chapter 5 --- General Discussions --- p.108 / Chapter 5.2 --- Research Overview --- p.108 / Chapter 5.2 --- Characterization of metal binding proteins from the cytosol of liver of tilapia --- p.109 / REFERENCES --- p.112