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<strong>JIOMICS</strong> | VOL 5 | ISSUE 2 | DECEMBER 2015 | 1-62<br />

JOURNAL OF INTEGRATED OMICS<br />

Journal of Integrated Omics<br />

A METHODOLOGICAL JOURNAL<br />

HTTP://WWW.<strong>JIOMICS</strong>.COM<br />

Special Issue: Proceeding Abstracts of the 4 th International Congress on Analytical Proteomics (ICAP 2015)<br />

Development and evaluation of method for metalloproteins detection<br />

involved in bipolar disorder<br />

G. S Pessôa* 1,2 , J. R. de Jesus 1,2 , A. Sussulini 1,2 , J. L. C. Martínez 3 ; M. A. Z. Arruda 1,2<br />

1<br />

Spectrometry, Sample Preparation, Mecanization Group, Analytical Chemistry Department, Institute of Chemistry, University of Campinas,<br />

P.O. box 6154, 13083970, Campinas, SP, Brazil. 2 National Institute of Science and Technology for Bioanalytics, Analytical Chemistry<br />

Department, Institute of Chemistry, University of Campinas, P.O. box 6154, 13083970, Campinas, SP, Brazil. 3 Bioscope group. Chemistry<br />

Department. Faculty of Sciences and Technology. New University of Lisbon. Campus de Caparica,. 2829-516. Caparica. Portugal.<br />

*Corresponding author: gpessoa@iqm.unicamp.br<br />

Available Online: 31 December 2015<br />

Abstract<br />

Purpose: Bipolar disorder (BD) is characterized as a chronic psychiatric illness, severe and highly debilitating, with recurrent mood disorders,<br />

presenting episodes of mania and depression separated by periods of normal behavior (Sussulini, et al., 2009;).The cause of bipolar<br />

disorder is unknown, although it is known that a variety of biochemical, genetic, and environmental factors can be involved in the process of<br />

developing of the disorder. To date, there is no biochemical test to confirm the disease, and the diagnosis is still based on experience and clinical<br />

judgment (Jesus, et al., 2015). The main focus of this work was to propose a metalloproteomic strategy for BD, since this area has been not<br />

carried out in the literature.<br />

Experimental description: Metal and metalloid ion involved in this pathology were determined by ICP-MS, using a dynamic reaction cell<br />

(Perkin Elmer, ELAN DRC-e). For metalloproteomic evaluation, a mild procedure for removal of major abundant protein was applied. For<br />

this task, a high performance liquid chromatograph was used to separate the proteins, using a sequential detection of proteins (UV-Vis) and<br />

metal ions (hyphenated LC-ICP-MS).<br />

Results: Considering the elemental determination, the DRC strategy was considered as an efficient method in the removal of interferences,<br />

since satisfactory results in terms of trueness and precision were obtained, using a certified reference material. Thus, an ionomic profile<br />

of each group was possible. After the chromatographic separation of proteins and metalloproteins, the removal of major abundant proteins is a<br />

main challenging step, since for a metallomic study, the information about tertiary structure must be preserved as intact as possible. The detection<br />

of proteins in UV-Vis and metalloproteins in LC-ICP-MS confirmed that our strategy was reliable for a metalloprotemic evaluation.<br />

Conclusions: Differential levels of metal and metalloid ions were observed when comparing the three studied groups, as well as the detection<br />

of metalloproteins by LC-ICP-MS. Thus, our method can be considered as reliable for evaluation of BD disorder.<br />

Keywords: bipolar disorder, metallomic, metalloprotein.<br />

Acknowledgements: FAPESP, FAEPEX, Capes and CNPq<br />

1-62: 7

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